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<description>Last 10 Controlled Substances Updates</description>
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<item>
	<title></title>
	<pubDate>Mon, 21 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/fluoro-n-methylcathinone.php</guid>
	<description><![CDATA[Flephedrone is a synthetic stimulant drug of the amphetamine and cathinone classes. It is chemically similar to the <a href='https://www.nonpsychotoxic.com/substances/cathinone.php'>cathinone compounds found in the khat plant</a> of eastern Africa. It comes in the form of a powder, which users can swallow, snort, inject or insert rectally producing effects which are somewhat similar to <a href='https://www.nonpsychotoxic.com/substances/mdma.php'>MDMA</a>, <a href='https://www.nonpsychotoxic.com/substances/amphetamine.php'>amphetamine</a>, and <a href='https://www.nonpsychotoxic.com/substances/cocaine.php'>cocaine</a>. Almost nothing is known about the long-term effects of flephedrone due to its short history of its use. The exact toxic dosage is unknown. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/psychonautwiki.php'><img src='/images/psychonautwiki.gif' alt='psychonautwiki.org' title='psychonautwiki.org' class='logo'></a>
<div class='talllink'>Excerpt from psychonautwiki.org: <br><a href='https://psychonautwiki.org/wiki/Talk:4-FMC'>
https://psychonautwiki.org/wiki/Talk:4-FMC</a>
</div></div>

<p>
<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/2mNXMDGZuYE" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <br>

<p>
<blockquote class='who'>
<b style='color: #d86422'>World Health Organization 2014:</b><br>
4-FMC, has emerged in recent years as a recreational psychostimulant. Its synthesis was first published in 1952 in order to explore the potential for antithyroidal, antibacterial and bacteriostatic properties. Publications about the detection of 4-FMC obtained from Internet sources and test purchases started to appear from 2009 onwards. The first official notification submitted to the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) by a European member state was 2008. Since then, it has been detected across the globe as a reflection of modern forms of trade within a globalised world. As was the case with many other emerging substances with psychoactive properties, commonly used terms include "legal highs", "bath salts" or "new psychoactive substances" (NPS) in the attempt to highlight the fact that many, if not most, did not originally fall under any legislative control and that detailed data on both pre-clinical and clinical levels were normally less well explored. The amount of research data on 4-FMC is comparatively small in comparison with other cathinones. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/who.php'><img src='/images/who.gif' alt='World Health Organization' title='World Health Organization' class='logo'></a>
<a href='https://legal-high-inhaltsstoffe.de/sites/default/files/uploads/flephedron_-_4-fmc.pdf'><img src='/images/4-FMC-who-pdf.png' alt='WHO PDF 4-FMC' class='pdf'></a>
<div class='pdflink'>World Health Organization 4-FMC (PDF 22 pages): <br><a href='https://legal-high-inhaltsstoffe.de/sites/default/files/uploads/flephedron_-_4-fmc.pdf'>
https://legal-high-inhaltsstoffe.de/sites/default/files/uploads/flephedron_-_4-fmc.pdf</a>
</div></div>
</blockquote>

<p>
On the drug forums, the users report effects comparable to <a href='https://www.nonpsychotoxic.com/substances/mdma.php'>MDMA</a> and <a href='https://www.nonpsychotoxic.com/substances/mephedrone.php'>mephedrone</a>. Flephedrone is usually administered orally, nasally or rectally over 2 -4 hour period in divided doses totaling 200-700 mg.  Some users find flephedrone less pleasurable, more addictive and "toxic" than <a href='https://www.nonpsychotoxic.com/substances/mephedrone.php'>mephedrone</a> and <a href='https://www.nonpsychotoxic.com/substances/methylone.php'>methylone</a>.  Fatigue, sleep deprivation and loss of appetite are the common after effects, similar to other cathinones. The recreational use of flephedrone was first reported in 2009
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/soft-tox.php'><img src='/images/softtox.gif' alt='soft-tox.org' title='soft-tox.org' class='logo'></a>
<img src='/images/4-FMC-soft-tox-pdf.png' alt='Soft Tox PDF 4-FMC' class='pdf'>
<div class='link'>Society of Forensic Toxicologists Flephedrone Monograph (PDF 2 pages): <br><span style='color: #DCDCDC;'>
https://www.soft-tox.org/files/designer_drugs/Flephedrone.pdf</span>
</div></div>




<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugs-forum.php'><img src='/images/drugs-forum.gif' alt='drugs-forum.com' title='drugs-forum.com' class='logo'></a>
<div class='link'>Drugs-Forum Experiences: <br><a href='https://drugs-forum.com/threads/flephedrone-4-fluoromethcathinone-4-fmc-experiences.96599/'>
https://drugs-forum.com/threads/flephedrone-4-fluoromethcathinone-4-fmc-experiences.96599/</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/erowid.php'><img src='/images/erowid.gif' alt='Erowid Experience Vaults' title='Erowid Experience Vaults' class='logo'></a>
<div class='link'>Erowid Vault 4-FMC: <br><a href='https://erowid.org/chemicals/4_fluoromethcathinone/'>
https://erowid.org/chemicals/4_fluoromethcathinone/</a>
</div></div>

<p>
<blockquote class='wikipedia'>
<b>Flephedrone:</b><br>
<ul><li>A stimulant drug of the cathinone chemical class
</li><li>Has been sold online as a designer drug starting in 2008.
</li></ul>
<p class='thumbsup'>Flephedrone has only a short history of human use and its toxicity is not well established</p>
</blockquote>
]]></description>
	<link>https://www.nonpsychotoxic.com/substances/fluoro-n-methylcathinone.php</link>
</item>

<item>
	<title></title>
	<pubDate>Sun, 20 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/synthetic-cannabinoids#mab-chminaca.php</guid>
	<description><![CDATA[<p>
<blockquote class='emcdda'>
<b>EMCDDA - Europol Joint Report 2017:</b><br>
ADB-CHMINACA appears to cause effects that resemble those of cannabis and other synthetic cannabinoids.
<p>
ADB-CHMINACA has been available in the European Union since at least August 2014 and has been detected in 18 Member States, Turkey and Norway. More than 600 seizures have been made within the European Union, which includes 7 kg of powder and 11 kg of herbal material which has been laced with ADB-CHMINACA. 
<p>
This herbal material is typically sold as smoking mixtures; the products are marketed as 'legal' replacements to cannabis. Due to the way that these products are produced, it appears that users are at risk of serious poisoning. 
<p>
There are indications that the AB-CHMINACA available on the market was synthesised by chemical companies based in China.Twelve deaths with confirmed exposure to ADB-CHMINACA have been reported by three Member States. In at least nine of the deaths, ADB-CHMINACA was the cause of death or contributed to the death.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/europol.php'><img src='/images/europol.gif' alt='Europol' title='Europol' height='30'></a><br><a href='https://www.nonpsychotoxic.com/sources/emcdda.php'><img src='/images/emcdda.gif' alt='European Monitoring Centre for Drugs and Drug Addiction' title='European Monitoring Centre for Drugs and Drug Addiction' class='logo'></a>
<a href='http://www.emcdda.europa.eu/system/files/publications/5485/2017.4966_TDAS17006ENN_PDFWEB.pdf'><img src='/images/adb-chminaca-emcdda.png' alt='ADB-CHMINACA Joint Report' class='pdf'></a>
<div class='tallpdflink'>Excerpt (PDF 15 pages): <br><a href='http://www.emcdda.europa.eu/system/files/publications/5485/2017.4966_TDAS17006ENN_PDFWEB.pdf'>
http://www.emcdda.europa.eu/system/files/publications/5485/2017.4966_TDAS17006ENN_PDFWEB.pdf</a>
</div></div>
</blockquote>

<p>
<blockquote class='who'>
<b style='color: #d86422'>World Health Organization 2018:</b><br>
First documented in international patent WO 2009/106980-A2 issued to Ingrid Buchler and colleagues at Pfizer on September 3, 2009. ADB-CHMINACA is also referred to as MAB-CHMINACA.
<p>
Case studies and reports of mass intoxication indicate that acute administration of ADB-CHMINACA has the potential to produce severe adverse reactions in humans up to, and including, death.  Symptoms of ADB-CHMINACA overdose may include tachycardia, unresponsiveness, seizures, delirium, slurred speech, vomiting, agitation and combativeness. In the spring of 2015, ADB-CHMINACA was associated with several drug-induced clusters of severe illness and death in the U.S. It has also been associated with 13 deaths in the European Union and one death in Japan.
<p class='who'>
White powder or crystalline solid.
</p>
The acute psychological effects of synthetic cannabinoids (including ADB-CHMINACA)may resemble those reported during acute intoxication with cannabis, ranging from a relaxed and unfocused euphoria to feelings of distress (e.g., confusion, anxiety, and fear).  Time perception may be distorted, and in susceptible individuals, hallucinations, paranoia, and more serious psychiatric disorder may occur.  Physical effects may include bloodshot eyes (as is characteristic of THC), tachycardia, nausea, vomiting, seizures, and impaired motor performance. Because synthetic cannabinoids are usually more potent (and also may be more efficacious) than phytocannabinoids, their effects occur at lower doses, and overdose may be more common, as suggested by increased reports of deaths and serious adverse reactions with this class of cannabinoids as compared to cannabis.11, 17-20Since users usually are unaware of which synthetic cannabinoid is contained in a product, they may administer a chemical with greater potency than the chemical contained in previous products.  Further, the chemical may not be evenly distributed throughout the plant material, creating "hot spots" containing higher concentrations of synthetic cannabinoid.  For these reasons, dose (in THC equivalents) often exceeds intended dose.  Contaminants (e.g., pesticides, heavy metals, rodent feces) may also be present and may contribute to adverse reactions.<p>
Case studies and reports of mass intoxication suggest that acute administration of ADB-CHMINACA has the potential to produce severe adverse reactions in humans up to, and including, death.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/who.php'><img src='/images/who.gif' alt='World Health Organization' title='World Health Organization' class='logo'></a>
<a href='https://www.who.int/medicines/access/controlled-substances/ADB_chmnaca.pdf'><img src='/images/adb-chmnaca-who-pdf.png' alt='WHO PDF ADB CHMNACA' class='pdf'></a>
<div class='pdflink'>Excerpt (PDF 18 pages): <br><a href='https://www.who.int/medicines/access/controlled-substances/ADB_chmnaca.pdf'>
https://www.who.int/medicines/access/controlled-substances/ADB_chmnaca.pdf</a>
</div></div>
</blockquote>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/swgdrug.php'><img src='/images/swgdrug.gif' alt='Science Working Group' title='Science Working Group' class='logo'></a>
<a href='https://www.swgdrug.org/Monographs/MAB-CHMINACA.pdf'><img src='/images/mab-chminaca-swgdrug-pdf.png' alt='SWGDRUG PDF MAB CHMINACA' class='pdf'></a>
<div class='pdflink'>MAB-Chminaca Monograph (PDF 5 pages): <br><a href='http://www.swgdrug.org/Monographs/MAB-CHMINACA.pdf'>
http://www.swgdrug.org/Monographs/MAB-CHMINACA.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/caymanchem.php'><img src='/images/caymanchemical.gif' alt='Cayman Chemical' title='Cayman Chemical' class='logo'></a>
<a href='https://www.caymanchem.com/msdss/16616m.pdf'><img src='/images/mab-chminaca-caymanchem-pdf.png' alt='CaymanChem PDF MAB CHMINACA' class='pdf'></a>
<div class='tallpdflink'>MAB-Chminaca Safety Data Sheet: <br><a href='https://www.caymanchem.com/msdss/16616m.pdf'>
https://www.caymanchem.com/msdss/16616m.pdf</a>
</div></div>

<p>
<blockquote class='wikipedia'>
<b>ADB-CHMINACA:</b><br>
<ul><li>An indazole-based synthetic cannabinoid
</li><li>Originally developed by Pfizer in 2009 as an analgesic medication
</li><li>It was identified in cannabinoid blends in Japan in early 2015
</li></ul>
<p class='update'>There have been a number of reported cases of deaths and hospitalizations in relation to this synthetic cannabinoid.</p>
</blockquote>
]]></description>
	<link>https://www.nonpsychotoxic.com/substances/synthetic-cannabinoids#mab-chminaca.php</link>
</item>

<item>
	<title></title>
	<pubDate>Thu, 17 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/methyl-2.php</guid>
	<description><![CDATA[<b>DOM</b>, a hallucinogen related to <a href='https://www.nonpsychotoxic.com/substances/mescaline.php'>mescaline</a> and <a href='https://www.nonpsychotoxic.com/substances/amphetamine.php'>amphetamine</a> and designated "STP" by hippies, along with <a href='https://www.nonpsychotoxic.com/substances/doet.php'>DOET</a>, the ethyl homologue of DOM, were given in small doses to normal subjects in a double-blind study. Both drugs increased self-awareness and produced mild euphoria but no hallucinogenic or psychotomimetic effects. The two drugs "freed up" subjects' word associations without impairing memory or concentration; in fact, DOM enhanced performance on serial learning tasks. Although DOM did not affect visual discrimination, it altered the perception of tachistoscopically presented TAT cards.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/psychiatryonline.php'><img src='/images/psychiatryonline.gif' alt='psychiatryonline.org' title='psychiatryonline.org' class='logo'></a>
<div class='link'>DOM (STP), a New Hallucinogenic Drug, and DOET: Effects in Normal Subjects: <br><a href='https://ajp.psychiatryonline.org/doi/abs/10.1176/ajp.125.3.357?journalCode=ajp'>
https://ajp.psychiatryonline.org/doi/abs/10.1176/ajp.125.3.357?journalCode=ajp<br>
</td></tr></table>




<p>
<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/CeFCkmuH4Uk" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <br>


<p>
<b>DOM:</b><br>
Is a psychedelic with strong stimulant qualities that has been used since the late 1960s. However, between the 1970s and 1990s, it was almost never used. The drug, which is also known as STP, has a relatively intense body high that can manifest as a feeling of energy and tingling through the body. Because it's a more stimulating psychedelic, it lends itself to physical activities. It may take a long time to begin working, which means you should avoid redosing anywhere near your initial administration. It'd be wise to avoid considering an extra dose for at least 4-5 hours. DOM hasn't caused death even with doses over 20-30 mg, but that doesn't mean those doses can be regarded as safe. While common doses do appear relatively safe for healthy people, you should minimize your use due to the lack of information.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/thedrugclassroom.php'><img src='/images/thedrugclassroom.gif' alt='The Drug Classroom' title='The Drug Classroom' class='logo'></a>
<div class='link'>The Drug Classroom: <br><a href='https://thedrugclassroom.com/video/dom/'>
https://thedrugclassroom.com/video/dom/</a>
</div></div>


<p class='eat'>
<b>DOM History:</b><br><br>
Dec 1, 1963<br>		DOM is first synthesized by Alexander Shulgin in 1963 and is first bio-assayed in December of that year. 
<br><br>
1967<br>		DOM (STP) first appears on the street in San Francisco, sometimes being confused with LSD and causing problems due to its long duration.
<br><br>
Jan 14, 1967<br>		Human Be-In in San Francisco is attended by 20,000. 5,000 doses of DOM (STP) were distributed for free, unfortunately, they were distributed in approximately 10-15 mg doses, 5-10 times higher than Shulgin had recommended.
<br><br>
Apr 2, 1968<br>		DOM (STP) was placed under DACA control in the United States, making it illegal to possess, sell, or manufacture except for personal use.
<br><br>
Sep 21, 1973<br> 		DOM is placed in <a href='https://www.nonpsychotoxic.com/definition.php?term=dea-schedules'>Schedule I of the CSA</a> in the U.S. making it illegal to buy, sell, or possess. <br>
<br>
- <a href='https://erowid.org/chemicals/dom/dom_timeline.php'>https://erowid.org/chemicals/dom/dom_timeline.php</a>
</p>


<p>
<b>STP:</b><br>
Slang for the long lasting psychedelic 2,5-dimethoxy-4-methylamphetamine, also known as DOM. STP was said to stand for Serenity, Tranquility, and Peace. Has properties related to <a href='https://www.nonpsychotoxic.com/substances/lysergic-acid-diethylamide.php'>LSD</a>. The high comes in at around half an hour after swallowing the tablet and is at peak at 2 to 3 hours depending on the quantity consumed. High can last 14 to 20 hours depending on dosage (14 to 20 according to 3 - 10 mg of STP consumed)
<ul><li>At 1 mg: Eyes dilated, mouth somewhat dry, and eerie feeling.
</li><li>At 2.3 mg: Mood elevation, emotional effects and colors become radiant.
</li><li>At 3 mg: Observation enhanced. Brighter and more colors
</li><li>At 4 mg: Arousing sensation. Colors intensify and slight hallucinations occur. Effects similar to <a href='https://www.nonpsychotoxic.com/substances/lysergic-acid-diethylamide.php'>LSD</a> and <a href='https://www.nonpsychotoxic.com/substances/mescaline.php'>Mescaline</a>.
</li><li>At 5 mg: Magnification of light, colors, and odors. Slight feeling of unhappiness along with joy. Hallucination occurs but can be stopped at will.
</li><li>At 8 mg: Music and visual warp into one being. "An off-beat fantasy."
</li><li>At 10 mg: Same as 8 mg, but effects come sooner and lasts a little longer.
</li><li>At 12 mg: Tremors, feeling of paralysis with music and visuals binding into an erotic fantasy.
</li></ul>Anyone planning on attempting to take STP should know that the effects may take up to an hour or two to show, so taking more dose is strictly unrecommended.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/urbandictionary.php'><img src='/images/urbandictionary.gif' alt='Urban Dictionary' title='Urban Dictionary' class='logo'></a>
<div class='link'>STP: <br><a href='https://www.urbandictionary.com/define.php?term=s.t.p.&page=2'>
https://www.urbandictionary.com/define.php?term=s.t.p.&page=2</a>
</div></div>

<p>
<table class='tripsit'>
<caption>DOM </caption>
<thead><tr><td colspan = '4'><b>Duration:</b><br>
<p class='eat'>The most popular psychedelic amphetamine due to its pleasant effects, lower potency and shorter duration. Effects have been described as 'sillier' than <a href='https://www.nonpsychotoxic.com/substances/lysergic-acid-diethylamide.php'>LSD</a> and related DOX chemicals</p></td></tr>
<tr><th style='text-align: left;'>
<b>Route</b></th><th>Onset</th><th>Duration</th><th style='text-align: right;'>After Effects</th></tr></thead>
<tfoot><tr><th colspan = '4'>Tripsit Factsheets</th></tr>
<tr><td colspan='4'>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/tripsit.php'><img src='/images/tripsit.gif' alt='Tripsit Factsheets' title='Tripsit Factsheets' class='logo'></a>
<div class='link'>DOM Basic Information: <br><a href='http://drugs.tripsit.me/dom'>
http://drugs.tripsit.me/dom</a>
</div></div>
</td></tr></tfoot>
<tbody>
<tr><td style='text-align: left;'><b>All ROAs:</b></td><td>2-4 hours</td><td>8-30 hours</td><td style='text-align: right;'>12-24 hours</td></tr>
<tr><td colspan = '4'><img src='/images/dom-duration-tripsit.gif' alt='DOM Duration' class='tripsit'>
</td></tr><tr><th colspan = '4'><b>Avoid:</b><br>
marijuana (Can potentiate effects)
</th></tr><tr><th colspan = '4'><b>Effects:</b><br>
visual distortions, a 'stoned' feeling, sense of well being.
</th></tr><tr><th colspan = '4'><b>Detection:</b><br>
DOM is a substituted amphetamine, so it can cause you to test positive for amphetamines 3 to 7 days after dosing.
</th></tr></tbody></table>


<p>
<b>Its use was short-lived due to its side effects:</b><br>
Over the years, DOM has gained a reputation for being a highly dose-sensitive psychedelic that is often sold on blotting paper and known for its strong visuals, body load and neutral, analytical headspace. Many reports also indicate that the effects of this chemical may be overly difficult to use for those who are not already experienced with psychedelics. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/psychonautwiki.php'><img src='/images/psychonautwiki.gif' alt='psychonautwiki.org' title='psychonautwiki.org' class='logo'></a>
<div class='talllink'>DOM Summary Sheet: <br><a href='https://psychonautwiki.org/wiki/DOM'>
https://psychonautwiki.org/wiki/DOM</a>
</div></div>


<p>
<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/lETfKJ04rmg" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <br>


<p>
<div class='source'><a href='https://erowid.org/experiences/subs/exp_DOM.shtml'><img src='/images/erowid.gif' alt='Erowid Experience Vaults' title='Erowid Experience Vaults' class='logo'></a>
<div class='link'>Erowid Experience Vault: <br><a href='https://erowid.org/experiences/subs/exp_DOM.shtml'>
https://erowid.org/experiences/subs/exp_DOM.shtml</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugs-forum.php'><img src='/images/drugs-forum.gif' alt='drugs-forum.com' title='drugs-forum.com' class='logo'></a>
<div class='link'>Experiences - DOM (STP): <br><a href='https://drugs-forum.com/threads/dom-stp-2-5-dimethoxy-4-methylamphetamine-experiences.42378/'>
https://drugs-forum.com/threads/dom-stp-2-5-dimethoxy-4-methylamphetamine-experiences.42378/</a>
</div></div>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/bluelight.php'><img src='/images/bluelight.gif' alt='Bluelight Forum' title='Bluelight Forum' class='logo'></a>
<div class='link'>The Big & Dandy DOM Thread (500 comments): <br>
https://www.bluelight.org/xf/threads/the-big-dandy-dom-thread.291980/
</div></div>



<p>
<b>A 1967 Newspaper Article:</b><br>
<img src='/images/stp-newspaperscom.gif' alt='' class='center'><br>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/newspapers.php'><img src='/images/newspapers.gif' alt='Newspapers.com' title='Newspapers.com' class='logo'></a>
<div class='link'>STP: <br><a href='https://www.newspapers.com/clip/39613954/dom-stp-article/'>
https://www.newspapers.com/clip/39613954/dom-stp-article/</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/pihkal.php'><img src='/images/pihkal.gif' alt='Pihkal' title='Pihkal' class='logo'></a>
<div class='link'>Pihkal DOM Entry: <br><a href='https://www.erowid.org/library/books_online/pihkal/pihkal068.shtml'>
https://www.erowid.org/library/books_online/pihkal/pihkal068.shtml</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/swgdrug.php'><img src='/images/swgdrug.gif' alt='Science Working Group' title='Science Working Group' class='logo'></a>
<a href='http://www.swgdrug.org/Monographs/2,5-dimethoxy-4-methylamphetamine.pdf'><img src='/images/dom-swgdrug-pdf.png' alt='SWGDRUG PDF DOM' class='pdf'></a>
<div class='pdflink'>2,5-Dimethoxy-4-methylamphetamine Monograph (PDF 5 pages): <br><a href='http://www.swgdrug.org/Monographs/2,5-dimethoxy-4-methylamphetamine.pdf'>
http://www.swgdrug.org/Monographs/2,5-dimethoxy-4-methylamphetamine.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/caymanchemical.php'><img src='/images/caymanchemical.gif' alt='Cayman Chemical' title='Cayman Chemical' class='logo'></a>
<a href='https://www.caymanchem.com/msdss/11145m.pdf'><img src='/images/dom-caymanchem-pdf.png' alt='Caymanchem PDF DOM' class='pdf'></a>
<div class='tallpdflink'>DOM Safety Data Sheet (PDF 6 pages): <br><a href='https://www.caymanchem.com/msdss/11145m.pdf'>
https://www.caymanchem.com/msdss/11145m.pdf</a>
</div></div>

<p>
<blockquote class='wikipedia'>
Effects of this drug include substantial perceptual changes such as blurred vision, multiple images, vibration of objects, visual alterations, distorted shapes, enhancement of details, slowed passage of time, increased sexual drive and pleasure, and increased contrasts. It may cause mystical experiences and changes in consciousness. It may also cause pupillary dilation and a rise in systolic blood pressure.
</blockquote>]]></description>
	<link>https://www.nonpsychotoxic.com/substances/methyl-2.php</link>
</item>

<item>
	<title></title>
	<pubDate>Thu, 17 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/methyl-n-ethylcathinone.php</guid>
	<description><![CDATA[<p>
<b>AKA Shrimp:</b><br>
4-MEC is an illegal stimulant, its chemical name is 4-Methylethcathinone. It is chemically similar to <a href='https://www.nonpsychotoxic.com/substances/mephedrone.php'>Mephedrone</a> and they are both cathinones. It is a white-powdered amphetamine like substance. It is mainly snorted, sometimes swallowed and acts on the central nervous system. 4-MEC can causes rapid heartbeat but also give a strong sense of well-being. It lasts an hour or more - you feel alert, exhilarated and very talkative. It was marketed and advertised as plant food or bath salts simply to get around medicine and consumer legislation. The price is relatively low (about 10-15 per gram) less than half the cost of cocaine but with much higher purity. It is much less prevalent than M-Cat.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/wnfo.php'><img src='/images/wnfo.gif' alt='WhyNotFindOut' title='WhyNotFindOut' class='logo'></a>
<div class='link'>4-MEC: <br><a href='http://www.wnfo.org.uk/drugs/4-mec/'>
http://www.wnfo.org.uk/drugs/4-mec/</a>
</div></div>


<p>
<table class='tripsit'>
<caption>4-MEC </caption>
<thead><tr><td colspan = '4'><b>Duration:</b><br>
<p class='eat'>A substituted cathinone stimulant; little is known about its safety or subjective effects. It is believed to have similar effects to <a href='https://www.nonpsychotoxic.com/substances/mephedrone.php'>mephedrone</a>, but with a lower potency and a stronger stimulating character.</p></td></tr>
<tr><th style='text-align: left;'>
<b>Route</b></th><th>Onset</th><th>Duration</th><th style='text-align: right;'>After Effects</th></tr></thead>
<tfoot><tr><th colspan = '4'>Tripsit Factsheets</th></tr>
<tr><td colspan='4'>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/tripsit.php'><img src='/images/tripsit.gif' alt='Tripsit Factsheets' title='Tripsit Factsheets' class='logo'></a>
<div class='link'>4-MEC Basic Information: <br><a href='http://drugs.tripsit.me/4-MEC'>
http://drugs.tripsit.me/4-MEC</a>
</div></div>
</td></tr></tfoot>
<tbody>
<tr><td style='text-align: left;'><b>Oral:</b></td><td>15-45 minutes</td><td>2-5 hours</td><td style='text-align: right;'>2-4 hours</td></tr>
<tr><td colspan = '4'><img src='/images/4-mec-duration-tripsit.gif' alt='4-MEC Duration' class='tripsit'>
</td></tr><tr><th colspan = '4'><b>Effects:</b><br>
Euphoria, increased energy/alertness, decreased need for sleep, increased sociability, mood lift, increased sexuality, excessive talking, decreased appetite, weight loss, sweating, disturbed sleep patterns, bruxism, visual and auditory hallucinations, itchiness, aggressiveness, moodiness.
</th></tr></tbody></table>

<p>
<blockquote class='who'>
<b style='color: #d86422'>World Health Organization 2016:</b><br>
4-Methylethcathinone (2-(ethylamino)-1-(4-methylphenyl)propan-1-one), also known as 4-MEC, has emerged in recent years as a recreational psychostimulant. Its homolog mephedrone (4-methylmethcathinone) is listed as a Schedule II substance under the 1971 United Nations Convention on Psychotropic Substances.The first official notification submitted to the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) by a European member state was 2010. Since then it has been detected across the globe and marketed as a "research chemical" although it has also been detected as a constituent in branded products available for purchase viathe Internet or brick-and-mortar shops. 
<p>
4-MEC is a psychostimulant with monoamine transporter activity with indications of abuse liability. Some data obtained from the analysis of user reports suggest that 4-MEC produces euphoria, a sense of well being,psychostimulant effects and lack of comedown symptomatology and that these appear to be less intense and short-lived compared to mephedrone. Conflicting information is available related to the urge of redosing, craving and bingeing. Negative effects associated with 4-MEC use include excessive sweating in the armpits, nausea, and vomiting but also jaw clenching, nystagmus, heart palpitations, loss of sightand migraine. 
<p class='who'>The available data so far also suggest that it may also function as a serotonin releasing agent but not dopamine, which would differentiate it from its homolog <a href='https://www.nonpsychotoxic.com/substances/mephedrone.php'>mephedrone</a>.</p>
Further studies are needed to assess the dependence potential.The number of case reports that demonstrate a causal relationship between 4-MEC consumption and fatal intoxication is relatively limited.There is no known therapeutic and medical use.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/who.php'><img src='/images/who.gif' alt='World Health Organization' title='World Health Organization' class='logo'></a>
<a href='https://www.who.int/medicines/access/controlled-substances/4.3_4-MEC_CritReview.pdf?ua=1'><img src='/images/methylethcathinone-who-pdf.png' alt='WHO PDF Methylethcathinone' class='pdf'></a>
<div class='pdflink'>4-Methylethcathinone (4-MEC)Critical Review Report (PDF 38 pages): <br><a href='https://www.who.int/medicines/access/controlled-substances/4.3_4-MEC_CritReview.pdf?ua=1'>
https://www.who.int/medicines/access/controlled-substances/4.3_4-MEC_CritReview.pdf?ua=1</a><br>
</div></div>
</blockquote>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/psychonautwiki.php'><img src='/images/psychonautwiki.gif' alt='psychonautwiki.org' title='psychonautwiki.org' class='logo'></a>
<div class='talllink'>4-MEC Summary Sheet: <br><a href='https://psychonautwiki.org/wiki/Talk:4-MEC'>
https://psychonautwiki.org/wiki/Talk:4-MEC</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/erowid.php'><img src='/images/erowid.gif' alt='Erowid Experience Vaults' title='Erowid Experience Vaults' class='logo'></a>
<div class='link'>4-Methylethcathinone Experience Reports: <br><a href='https://www.erowid.org/experiences/subs/exp_4Methylethcathinone.shtml'>
https://www.erowid.org/experiences/subs/exp_4Methylethcathinone.shtml</a>
</div></div>



<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/swgdrug.php'><img src='/images/swgdrug.gif' alt='Science Working Group' title='Science Working Group' class='logo'></a>
<a href='https://www.swgdrug.org/Monographs/4-MEC.pdf'><img src='/images/methylethcathinone-swgdrug-pdf.png' alt='SWGDRUG PDF Methylethcathinone' class='pdf'></a>
<div class='pdflink'>4-methylethcathinone Monograph (PDF 5 pages): <br><a href='http://www.swgdrug.org/Monographs/4-MEC.pdf'>
http://www.swgdrug.org/Monographs/4-MEC.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/caymanchemical.php'><img src='/images/caymanchemical.gif' alt='Cayman Chemical' title='Cayman Chemical' class='logo'></a>
<a href='https://www.caymanchem.com/msdss/9001069m.pdf'><img src='/images/methylethcathinone-caymanchem-pdf.png' alt='Caymanchem PDF Methylethcathinone' class='pdf'></a>
<div class='tallpdflink'>4-Methylethcathinone (hydrochloride) Safety Data Sheet (PDF 5 pages): <br><a href='https://www.caymanchem.com/msdss/9001069m.pdf'>
https://www.caymanchem.com/msdss/9001069m.pdf</a>
</div></div>
]]></description>
	<link>https://www.nonpsychotoxic.com/substances/methyl-n-ethylcathinone.php</link>
</item>

<item>
	<title></title>
	<pubDate>Thu, 17 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/methandriol.php</guid>
	<description><![CDATA[<blockquote class='ncats'>
Methandriol is an anabolic steroid. Methandriol is classified as a weak anabolic with weak androgenic properties. Methandriol displays some level of estrogenic activity, making this steroid less useful for dieting. The drug is generally considered too mild and is not widely popular among bodybuilders and athletes. It seems most prominent in Australia now, where it remains included in a number of veterinary anabolic steroid products.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/ncats.php'><img src='/images/ncats.gif' alt='NCATS' title='NCATS' class='logo'></a>
<div class='link'>Methandriol: <br><a href='https://drugs.ncats.io/drug/8XIW70Q5I3'>
https://drugs.ncats.io/drug/8XIW70Q5I3</a>
</div></div>
</blockquote>

<p>
Methylandrostenediol (methandriol for short) is an anabolic steroid derived from <a href='https://www.nonpsychotoxic.com/substances/dihydrotestosterone.php'>dihydrotestosterone</a>. The drug itself is manufactured in two very distinct forms. The first is unesterified (straight) methylandrostenediol, which is used when making an oral medication with this steroid (although an injectable once existed in the U.S.). It is also found as esterified methylandrostenediol dipropionate, which is prepared as an injectable. The added propionate esters in the injectable form extend the activity of the drug for several days. Basically, methandriol drugs are altered c17-alkylated forms of 5-androstenediol. Methandriol is classified as a weak anabolic with weak androgenic properties. It also seems to display some level of estrogenic activity, making this steroid less ideal for dieting. The drug is generally considered too mild, and is not widely popular among bodybuilders and athletes. Sometimes, however, it is used in place of other anabolic/androgenic agents in bulking stacks when available.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/anabolicorg.php'><img src='/images/anabolicorg.gif' alt='anabolic.org' title='anabolic.org' class='logo'></a>
<div class='link'>Steroid Profiles - Methandriol and Methandriol Dipropionate: <br><span style='color: #DCDCDC;'>
https://anabolic.org/methandriol-dipropionate/</span>
</div></div>

<p>
<b>One of the more rare and exotic anabolic steroids:</b><br>
Methandriol (or MAD as I like to call it) seems to be one of the more rare and exotic anabolic steroids. It is actually 5-androstenediol (5AD) that has had its chemical structure modified by adding a methyl group so the compound can resist being broken-down by the liver when taken orally. This results in better utilization by the body and is called 17-alpha alkylation (17AA). The first aspect that will be addressed is the one that most interests bodybuilders, the muscle building potential of the drug. With an anabolic (muscle building) effect of 20-60 (compared <a href='https://www.nonpsychotoxic.com/substances/testosterone.php'>testosterone</a> which has an anabolic rating of 100), not much muscle gain can be expected from MAD use. It is also slightly androgenic, again when compared to testosterone which has an androgenic effect of 100 MAD only rates 30-60. Methandriol low androgenic properties may be a blessing and a curse, on one hand with its low androgenic effects the drug can be used without worries by prone individuals who suffer from prostate problems, hair loss and acne. It may also be used by female bodybuilders who wish to avoid the masculinizing side effects of androgens once they stick to a reasonable dosage and cycle duration. On the other hand the benefits of using an androgenic steroid are lost, there is a direct correlation between a drugs androgenic levels and strength gains, highly androgenic steroids also tend to aid in fat loss by binding strongly to the androgen receptor (A.R). So not much muscle or strength gain from this one. So what the hell is it good for? Glad you asked. Methandriol has been shown to have an affinity for glucocorticoid-binding sites so this may result in an anti-catabolic (muscle destroying) effect by inhibiting the muscle wasting effects of glucocorticoid hormones also the parent hormone of methandriol, 5-androstenediol (5AD) has been shown to promote favorable immune function.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/steroidcom.php'><img src='/images/steroidcom.gif' alt='steroid.com' title='steroid.com' class='logo'></a>
<div class='talllink'>Steroid Profiles - Methandriol: <br><a href='https://www.steroid.com/Methandriol.php'>
https://www.steroid.com/Methandriol.php</a>
</div></div>

<p>
<b>Magnifies the effects of other steroids:</b><br>
The best results can be obtained, however, if Methandriol Dipropionate is not taken alone but in combination with another steroid. This is because Methandriol Dipropionate is able to magnify the effects of other steroid compounds. It does this by increasingly sensitizing the androgenic receptors of the muscle cell, allowing a higher amount of the steroid molecules of the additionally taken steroids to be absorbed by the receptors. This also explains why injectable Methandriol Dipropionate is only available today as a combination compound with an additional steroid substance. Injectable Methandriol Dipropionate is only available in the Australian veterinary steroids Drive, Spectriol, Geldabol, and Filibol Forte so that procurement of the compound is difficult. The few athletes using this drug report good strength gains, a solid muscle gain, and low water retention. The combination steroids aromatize only slightly so, when taking only Methandriol Dipropionate, the use of antiestrogens is perhaps appropriate. The injectable form is only slightly toxic.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/worldofchemicals.php'><img src='/images/worldofchemicals.gif' alt='World of Chemicals' title='World of Chemicals' class='logo'></a>
<div class='link'>Steroid Hormone Powder Methandriol Dipropionate: <br><a href='https://www.worldofchemicals.com/chemicals/chemical-suppliers/99-purity-high-quality-steroid-hormone-powder-methandriol-dipropionate-3593-85-9.html'>
https://www.worldofchemicals.com/chemicals/chemical-suppliers/99-purity-high-quality-steroid-hormone-powder-methandriol-dipropionate-3593-85-9.html</a>
</div></div>

<p>
<b>Tissue Repair:</b><br>
Methandriol comes as an injectable form and oral pills, all of which are highly bio-available. Its powerful tissue-formulation properties and amazing muscle-building properties make it a popular option in the sporting world. It has been supported by the fact that it can stimulate hormones responsible for tissue repair without having any adverse effects such as virilization. It is the reason it has been used for many years as a tissue-builder.
<p>
<div class='source'><img src='/images/anabolicsteroiddrugs.gif' alt='anabolicsteroiddrugs.com' title='anabolicsteroiddrugs.com' height='80' class='logo'>
<div class='link'>A Robust Description Of Methandriol: <br><span style='color: #DCDCDC;'>
https://anabolicsteroiddrugs.com/methandriol/</span>
</div></div>

<p>
<b>Methylandrostenediol History:</b><br>
Methylandrostenediol was first described in 1935, making this a very old agent as far as synthetic anabolic steroids are concerned. Methylandrostendiol was developed into a medicine by Organon, which sold it in the United States under the Stenediol brand name in both oral (methylandrostenediol) and injectable (methylandrostendiol dipropionate) forms. Many other generics and other brands of methylandrostenediol soon followed, and the drug was a popular anabolic agent in the United States during the 1950's. Methylandrostenediol was essentially the first steroid perceived to have a notable separation of anabolic (higher) and androgenic (lower) effect, a persistent goal of pharmaceutical developers. Early product literature described it as, "a steroid which has considerable of the male hormone's tissuebuilding action without to the same extent causing virilization." It was indicated for use as a, "tissue-builder in cases of retarded growth or failure to gain weight accompanied by protein wastage, negative nitrogen balance, or failure to build body proteins." Early assessments of methylandrostenediol being primarily anabolic in nature did not hold up well with later extensive use in humans. It was eventually determined that in doses sufficient to promote weight gain, its anabolic properties were accompanied by significant androgenic activity. Ultimately, this drug would be viewed as one of balanced anabolic and androgenic action, not as a highly anabolic agent as originally thought. Organon would go on to develop more effective anabolic agents, such as their 19-nor series of drugs including <a href='https://www.nonpsychotoxic.com/substances/nandrolone.php'>Durabolin, Deca-Durabolin</a>, and <a href='https://www.nonpsychotoxic.com/substances/ethylestrenol.php'>Maxibolin</a>, and eventually discontinued the Stenediol Methandriol products. The other U.S. brand and generic forms of the drug would follow as well, although methylandrostenediol would persist in the U.S. scene for some time. Currently, no domestic source of the drug exists, although it is still found in certain international markets. It seems most prominent in Australia at the present time, where it remains included in a number of veterinary anabolic steroid products. 
<p>
<b>Methylandrostenediol Side Effects:</b><br>
<ul><li>Estrogenic
</li><li>Androgenic
</li><li>Hepatotoxicity
</li><li>Cardiovascular
</li><li>Testosterone Suppression
</li></ul>
<p class='eat'>
This drug is derived from <a href='https://www.nonpsychotoxic.com/substances/androstenediol.php'>androstenediol</a>, which is a metabolite of <a href='https://www.nonpsychotoxic.com/substances/testosterone.php'>testosterone</a>. It has not been seen in any form for several years in the athletic community. Just recently though it has shown up in a couple of new vet drugs from Australia; Spectriol and Drive. Methandriol itself is a high anabolic, high androgenic steroid. It is used for strength and weight gains. Some lifters feel it works well stacked with injectable testosterones. One claim is that it enhances receptor stimulation, causing the drug it is stacked with to bind better to androgen sites at the cell. Perhaps this is why the two new drugs previously mentioned are combination drugs. Methandriol will aromatise and it is moderately toxic. A popular counterfeit, Abolic injection or Metabolin claimed to be Methandriol dipropionate. It was quite abundant on the market, but has pretty much disappeared from the market at this time. 
</p>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/steroidsworld.php'><img src='/images/steroidsworld.gif' alt='Steroids World' title='Steroids World' class='logo'></a>
<div class='link'>Steroid profiles | Anabolic / Androgenic Steroids| Methandriol - methylandrostenediol: <br><a href='https://steroid.to/methandriol-methylandrostenediol'>
https://steroid.to/methandriol-methylandrostenediol</a>
</div></div>

<p>
<b>The possible side effects of Methandriol Dipropionate pills:</b><br>
<ul><li>The liver increase secretion
</li><li>The gastrointestinal affections
</li><li>The acne
</li><li>The ginaecomasthy
</li><li>An expanded aggressiveness
</li><li>An easy arterial tension increase
</li></ul>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/blogger.php'><img src='/images/blogger.gif' alt='Blogger' title='Blogger' class='logo'></a>
<div class='link'>Roid Powers Blog: <br><a href='http://roidpowders.blogspot.com/2016/11/what-is-methandriol-dipropyonate.html?m=0'>
http://roidpowders.blogspot.com/2016/11/what-is-methandriol-dipropyonate.html?m=0</a>
</div></div>

<p>
<b>Methandriol is a poor anabolic:</b><br>
Methandriol dipropionate, used in some Australian veterinary products, is to be avoided by male bodybuilders. It is highly estrogenic, and has no redeeming properties. Methandriol is a poor anabolic and the mythical "receptor-cleaning" properties that have been claimed for it are pure fantasy. An anti-aromatase would not correct the estrogenic problems of methandriol dipropionate, since it is directly estrogenic, not requiring conversion by aromatase. An anti-estrogen such as Clomid would probably help, but since methandriol is a poor anabolic anyway, there is no point to a methandriol/Clomid stack.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/thinksteroids.php'><img src='/images/thinksteroids.gif' alt='thinksteroids.com' title='thinksteroids.com' class='logo'></a>
<div class='link'>Anabolic Steroids and Performance-Enhancing Drugs / Methandriol Dipropionate: <br><a href='https://thinksteroids.com/steroid-profiles/methandriol-dipropionate/'>
https://thinksteroids.com/steroid-profiles/methandriol-dipropionate/</a>
</div></div>

<p>
<b>Methandriol is rather unheard of:</b><br>
Methandriol (MAD, as bodybuilders often refer to it) is a rather unheard of steroid for most people. For those familiar with the brief-lived popularity of prohormones as nutritional supplements, Methandriol's chemical name, "Methylandrostendiol" will sound more familiar . Methandriol is simply the prohormone 5-androstendiol, altered to be orally available. MAD is an Anabolic/Androgenic steroid which reportedly improves receptor affinity for/with other anabolic/androgenic compounds. This is why it has been added to several veterinary compounds, in small doses, such as Libriol, Drive, Spectriol, and Tribolan. It can provide good muscle gains along with good strength gains, and unfortunately causes high water retention as well. MAD 's supposed ability to "clean out" or potentiate androgen receptor sites is certainly possible (as other drugs have been known to increase androgen receptor concentration and number), but literature on it is scarce. In bodybuilding circles, this is it's claim to fame, however. Reportedly, long-term steroid users who had experienced so called receptor burn-out, or a possible decrease in receptor number or concentration were able to use MAD to renew gains. Recently, British Dragon has brought a solo Methandriol product to the market, and this is, at the time of this writing the only legitimate one being produced in the world today. 
<p>
<div class='source'><img src='/images/blank.gif' alt='' title='' height='30' class='logo'>
<div class='link'>Thread: Methandriol Dipropionate (methyldrostenediol Dipropionate): <br><a href='http://infinitymuscle.com/threads/40-Methandriol-Dipropionate-(methyldrostenediol-Dipropionate)'>
http://infinitymuscle.com/threads/40-Methandriol-Dipropionate-(methyldrostenediol-Dipropionate)</a>
</div></div>

<p>
<b>Primarily manufactured for use in veterinary medicine:</b><br>
Methylandrostenediol is an anabolic steroid that gained popularity because of its reputation for putting on significant body mass to meat producing animals, with these results attempting to be reproduced by steroid users. The steroid utilizes 17 alpha alkylation as to better prepare the compound to resist being broken down by the liver when ingested orally. As stated, it is still primarily manufactured for use in veterinary medicine as a means to help increase weight gain in meat producing animals and was first marketed in the 1980s. For strength athletes and bodybuilders it is thought to produce weight gain in users when used in adequate doses, although these gains often result in both increases in muscle as well as water retention and body fat due to the unique characteristics of the compound.
<p>
<div class='source'><img src='/images/canadabodybuilding.gif' alt='canadabodybuilding.com' title='canadabodybuilding.com' height='30' class='logo'>
<div class='link'>Methandriol Dipropionate: <br><span style='color: #DCDCDC;'>
http://www.canadabodybuilding.com/showthread.php?6078-Methylandrostenediol-Methandriol-Profile</span>
</div></div>

<p>
<b>Methandriol is not really an actual steroid. It's more of a prohormone:</b><br>
Its only illegal because it's either esterized or methylated, both practices declaring any steroidal substance illegal by the catch clause for schedule III drugs. But basically its 5-androstene-3beta, 17beta-diol, better known as 5AD. A prohormone that is legally available in pure form and a rather weak one at that. Being a prohormone it means it needs to interact with an enzyme to form the active substrate. In this case 5AD is a testosterone precursor, but it only yields about 0.19% of testosterone upon interaction with the 3beta hydroxysteroid dehydrogenase enzyme1 it uses to convert. So in terms of active anabolic compounds you see MAD is weaker than weak. Even in legal circles 5AD isn't really used very often because there are better substances available. So what's really the use of MAD? Well it seems 5AD is a potent estrogen agonist. That means it doesn't necessarily act as an estrogen and it certainly doesn't convert to an estrogen, but that it increases the effect of circulating estrogens from other compounds. This makes MAD quite capable of increasing bulk weight (water and/or fat) quite well when stacked with a substance that aromatizes heavily, such as methandrostenolone or testosterone. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/elitefitness.php'><img src='/images/elitefitness.gif' alt='elitefitness.com' title='elitefitness.com' class='logo'></a>
<div class='talllink'>Methandriol Dipropionate? (2004): <br><a href='https://www.elitefitness.com/forum/anabolic-steroids/methandriol-dipropionate-336738.html'>
https://www.elitefitness.com/forum/anabolic-steroids/methandriol-dipropionate-336738.html</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/juicedmuscle.php'><img src='/images/juicedmuscle.gif' alt='juicedmuscle.com' title='juicedmuscle.com' class='logo'></a>
<div class='link'>Methandriol Dipropionate: <br><a href='https://juicedmuscle.com/jmblog/content/methandriol-dipropionate-0'>
https://juicedmuscle.com/jmblog/content/methandriol-dipropionate-0</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/swgdrug.php'><img src='/images/swgdrug.gif' alt='Science Working Group' title='Science Working Group' class='logo'></a>
<a href='https://www.swgdrug.org/Monographs/Methandriol.pdf'><img src='/images/methandriol-swgdrug-pdf.png' alt='SWGDRUG PDF Methandriol' class='pdf'></a>
<div class='pdflink'>Methandriol Monograph (PDF 5 pages): <br><a href='http://www.swgdrug.org/Monographs/Methandriol.pdf'>
http://www.swgdrug.org/Monographs/Methandriol.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/inchem.php'><img src='/images/inchem.gif' alt='Inchem' title='Inchem' class='logo'></a>
<div class='link'>Methandriol Monograph: <br><a href='http://www.inchem.org/documents/pims/pharm/pim906.htm'>
http://www.inchem.org/documents/pims/pharm/pim906.htm</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/wikipedia.php'><img src='/images/wikipedia.gif' alt='Wikipedia' title='Wikipedia' class='logo'></a>
<div class='link'>Methandriol dipropionate (MADP): <br><a href='https://en.wikipedia.org/wiki/Methandriol_dipropionate'>
https://en.wikipedia.org/wiki/Methandriol_dipropionate</a>
</div></div>
]]></description>
	<link>https://www.nonpsychotoxic.com/substances/methandriol.php</link>
</item>

<item>
	<title></title>
	<pubDate>Thu, 17 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/methenolone.php</guid>
	<description><![CDATA[<blockquote class='ncats'>
Methenolone (also known as primobolan) was described in 1960. Squibb Company began producing injectable drug in 1962. Methenolone originally was prescribed in case of muscle loss after operations, infections, long-term illnesses, aggressive therapy with corticoids or malnutrition, and in some cases it was used to treat osteoporosis and breast cancer. Methenolone was commonly used to promote weight gain in infants, weighing less than normal, without any side effects. Methenolone is an anabolic steroid, modification of dihydrotestosterone (DHT) with weak androgenic activity and a moderate anabolic effect. A notable trait of methenolone is that it can firmly bind to androgen receptors, stronger than <a href='https://www.nonpsychotoxic.com/substances/testosterone.php'>testosterone</a>. Adult doses for the treatment of aplastic anemia are usually in a range of 1 - 3 mg/kg per day. <p>Adverse side effects include fluid and electrolyte retention, hypercalcaemia, increased bone growth and skeletal weight. In men, additional side priapism, azoospermia, hirsutism, male pattern baldness, acne andoedema. In women, side effects include virilization, amenorrhoea, menstrual irregularities, suppressed lactation, and increased libido. In children, side effects may include virilization symptoms. Metenolone may enhance effects of antidiabetics, ciclosporin, levothyroxine, warfarin. Resistance to the effects of neuromuscular blockers may occur, and metenolone also has the potential to interfere with glucose tolerance and thyroidfunction tests. Metenolone enanthate (methenolone enanthate) is an ester derivative of methenolone sold commonly under the brand names Primobolan (tablet form) orPrimobolan Depot (injectable). When it interacts with the aromatase enzyme it does not form any estrogens. It is used by people who are very susceptible to estrogenic side effects, having lowerestrogenic properties than <a href='https://www.nonpsychotoxic.com/substances/nandrolone.php'>nandrolone</a>. This trait makes primobolan to be a good fat burner. Primobolan does not convert into estradiol. <p>As an anabolic steroid, the use of metenolone is banned from use in sports governed by the World Anti-Doping Agency. Belarusian shot putter Nadzeya Ostapchuk was stripped of her gold medal after testing positive for metenolone at the London 2012 Olympic Games. She has been excluded from future IOC events. The NBA and NBPA also banned the use of methenolone under the Anti-Drug Program. In February 2013, Hedo Turkoglu of the Orlando Magic was suspended for 20 games without pay by the league after testing positive for methenolone. In December 2013, Natalia Volgina was stripped of her 2013 Old Mutual Two Oceans Marathon title and received a two-year competition ban, subsequent to a final guilty verdict for using the steroid Metenolone.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/ncats.php'><img src='/images/ncats.gif' alt='NCATS' title='NCATS' class='logo'></a>
<div class='link'>Methenolone: <br><a href='https://drugs.ncats.io/drug/9062ZT8Q5C'>
https://drugs.ncats.io/drug/9062ZT8Q5C</a>
</div></div>
</blockquote>

<p>
<b>Began as a Starter Steroid:</b><br>
Many beginners make first steroid experiences with methenolone. It is milder than many other steroids and has significantly fewer side effects. However, the weight gain and the increase in force are also significantly lower than by other steroids.
<p>
Metenolon was then much sought after and considered as a very mild steroid. In the end, it was not so mild and free of side effects, as we have seen today. For a long time, Metenolon was considered a starter steroid. For bodybuilders who have already had experience with stronger steroids, methenolone (neither in the acetate nor in the enatate form) is suitable neither for the build-up nor for the settling phase to maintain the muscle mass.
<p>
General experience of bodybuilders who have taken methenolone speak of a mass increase of just 3 - 4 kg in 6 weeks. The tablet version (metelonone acetate) is, however, discouraged, since the active ingredient is very poorly absorbed and is therefore no longer available for the purpose to be fulfilled. In order to achieve a better efficiency, body builders usually use the injection-variant (Methenolonenantat).
<p>
Methenolone acetate products (tablets) today come mainly from Japan and South Africa.
Today, methenolonenate products (ampoules) come mainly from Mexico, Spain and Turkey.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/anabolikade.php'><img src='/images/anabolikade.gif' alt='anabolika.de' title='anabolika.de' class='logo'></a>
<div class='link'>Methenolone: <br><a href='https://anabolika.de/en/methenolone'>
https://anabolika.de/en/methenolone</a>
</div></div>

<p>
<b>A mild nature:</b><br>
Primobolan is nowhere near the most popular or powerful anabolic steroid on the market. But it is still popular, maybe for a different reason. The compound seems to hold potential for great results if used for the correct purpose. It is said to be one of Arnold Schwarzenegger's favorite steroids. You may conclude the benefits are obvious in that case if the rumors are true. Primobolan is a popular trade name of the anabolic and androgen steroid methenolone. This compound is familiar to many experienced steroid users, who often call it "Primo." It has a mild nature that makes it more tolerable to use compared to many other steroids. This drug is often compared to another popular anabolic steroid <a href='https://www.nonpsychotoxic.com/substances/oxandrolone.php'>Anavar</a>. But Primobolan is actually milder than Anavar. It has an androgenic rating between 44 and 57 and an anabolic rating of 88. Both ratings are even lower than those of testosterone.

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/gilmorehealth.php'><img src='/images/gilmorehealth.gif' alt='gilmorehealth.com' title='gilmorehealth.com' class='logo'></a>
<div class='link'>Primobolan A Popular Steroid Amongst Athletes for Its Limited Side Effects: <br><a href='https://www.gilmorehealth.com/primobolan-a-popular-steroid-amongst-athletes-for-its-limited-side-effects/'>
https://www.gilmorehealth.com/primobolan-a-popular-steroid-amongst-athletes-for-its-limited-side-effects/</a>
</div></div>



<p>
<blockquote class='hmdb'>
<b>Anabolic Steroid:</b><br>
Metenolone (or methenolone) is a long-acting anabolic steroid with weak androgenic (testosterone or androsterone-like) properties. It is a naturally occurring drug, found within the adrenal glands of pregnant domesticated felines, and is supplied as the acetate ester for oral administration and as the enanthate ester for intramuscular injection. Adult doses for the treatment of aplastic anemia are usually in a range of 1-3 mg/kg per day. Belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/hmdb.php'><img src='/images/hmdb.gif' alt='hmdb.ca' title='hmdb.ca' class='logo'></a>
<div class='link'>Metabocard for Methenolone: <br><a href='https://hmdb.ca/metabolites/HMDB0041928'>
https://hmdb.ca/metabolites/HMDB0041928</a>
</div></div>
</blockquote>


<p>
<b>What are Primobolan side effects/dangers?</b><br>
Primobolan may be milder than other anabolic steroids and promise safer results; however, misuse - like with all things - can result in some pretty nasty side effects. Even though there aren't many scientific studies on the drug (aside from on rats), people who have used the steroid have reported many bad side effects. Common Primobolan side effects include: depression, acne, oily skin, hair loss/balding, excess body hair, increases in bad cholesterol, and gynecomastia (this usually only occurs if it has been stacked with another anabolic steroid). Obviously, if you keep to safe, lower dosages, the chance of these side effects happening should be minimal. However, we do advise leaning on the side of caution - especially if you are already predisposed to them e.g. you've got sensitive skin. Women especially should be careful.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/crazybulk.php'><img src='/images/crazybulk.gif' alt='crazybulk.com' title='crazybulk.com' class='logo'></a>
<div class='link'>Primobolan Depot Steroid (Methenolone) - Cycle, Dosage & Side Effects: <br><a href='https://crazybulk.com/blog/primobolan-depot-methonolone'>
https://crazybulk.com/blog/primobolan-depot-methonolone</a>
</div></div>


<p>
<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/ljviMEFeWaQ" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <br>
<p>
<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/clt3YRTSTDo" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <br>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/caymanchemical.php'><img src='/images/caymanchemical.gif' alt='Cayman Chemical' title='Cayman Chemical' class='logo'></a>
<a href='https://www.caymanchem.com/msdss/17148m.pdf'><img src='/images/primobolan-caymanchem-pdf.png' alt='Caymanchem PDF Primovolan' class='pdf'></a>
<div class='tallpdflink'>Primobolan Safety Data Sheet (PDF 6 pages): <br><a href='https://www.caymanchem.com/msdss/17148m.pdf'>
https://www.caymanchem.com/msdss/17148m.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/thinksteroids.php'><img src='/images/thinksteroids.gif' alt='thinksteroids.com' title='thinksteroids.com' class='logo'></a>
<div class='link'>Primobolan discussion: <br><a href='https://thinksteroids.com/community/threads/lets-talk-about-primobolan.134381483/'>
https://thinksteroids.com/community/threads/lets-talk-about-primobolan.134381483/</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/canadianbrawn.php'><img src='/images/canadianbrawn.gif' alt='canadianbrawn.com' title='canadianbrawn.com' class='logo'></a>
<div class='link'>Primobolan discussion: <br><a href='https://canadianbrawn.com/threads/what-does-primobolan-metenolone-enanthate-do-for-you.814/'>
https://canadianbrawn.com/threads/what-does-primobolan-metenolone-enanthate-do-for-you.814/</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/gymnation.php'><img src='/images/gymnation.gif' alt='gymnation.co.nz' title='gymnation.co.nz' class='logo'></a>
<div class='link'>Primobolan discussion: <br><a href='http://www.gymnation.co.nz/forums/topic/10131-primobolan-opinions-from-personal-experiences/'>
http://www.gymnation.co.nz/forums/topic/10131-primobolan-opinions-from-personal-experiences/</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/tnation.php'><img src='/images/tnation.gif' alt='T-Nation Forum' title='T-Nation Forum' class='logo'></a>
<div class='link'>50+ results for Primobolan: <br><a href='https://forums.t-nation.com/search?q=primobolan'>
https://forums.t-nation.com/search?q=primobolan</a>
</div></div>


<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/instagram.php'><img src='/images/instagram.gif' alt='instagram.com' title='instagram.com' class='logo'></a>
<div class='link'>#methenolone: <br><a href='https://www.instagram.com/explore/tags/methenolone/?hl=en'>
https://www.instagram.com/explore/tags/methenolone/?hl=en</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/thecanadianpharm.php'><img src='/images/thecanadianpharm.gif' alt='thecanadianpharm.com' title='thecanadianpharm.com' class='logo'></a>
<a href='http://thecanadianpharm.com/images/products_images/primobolan.pdf'><img src='/images/primobolan-thecanadianpharm-pdf.png' alt='thecanadianpharm PDF Primovolan' class='pdf'></a>
<div class='pdflink'>Primobolan Package Leaflet (PDF 2 pages): <br><a href='http://thecanadianpharm.com/images/products_images/primobolan.pdf'>
http://thecanadianpharm.com/images/products_images/primobolan.pdf</a>
</div></div>

<p>
<blockquote class='wikipedia'>
Metenolone esters are used mainly in the treatment of anemia due to bone marrow failure. Side effects of metenolone esters include symptoms of masculinization like acne, increased hair growth, voice changes, and increased sexual desire. Metenolone esters are synthetic androgens and anabolic steroids. They have moderate anabolic effects and weak androgenic effects, as well as no estrogenic effects or risk of liver damage. Metenolone esters were introduced for medical use in the early 1960s. In addition to their medical use, metenolone esters are used to improve physique and performance. The drugs are controlled substances in many countries and so non-medical use is generally illicit. They have mostly been discontinued for medical use and have limited availability.
</blockquote>]]></description>
	<link>https://www.nonpsychotoxic.com/substances/methenolone.php</link>
</item>

<item>
	<title></title>
	<pubDate>Thu, 17 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/methylone.php</guid>
	<description><![CDATA[<blockquote class='ncats'>
Methylone (3, 4-Methylenedioxy-N-methylcathinone), a B-keto analog of 3,4-methylenedioxy-N-methylamphetamine (MDMA) is a stimulant and psychoactive drug. Methylone is a popular drug of abuse that strongly increases the release of the three monoamines: dopamine, serotonin (5-HT) and norepinephrine. In addition, methylone inhibits plasma membrane catecholamine transporters but only weakly inhibit the vesicle transporter. In April 2013, methylone was listed in the Schedule 1 substance under the Controlled Substances Act.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/ncats.php'><img src='/images/ncats.gif' alt='NCATS' title='NCATS' class='logo'></a>
<div class='link'>Methylone: <br><a href='https://drugs.ncats.io/drug/L4I4B1R01F'>
https://drugs.ncats.io/drug/L4I4B1R01F</a>
</div></div>
</blockquote>

<p>
Methylone is sometimes used as a substitute for MDMA due to similarities in their effects. Alexander Shulgin commented that the substances has "almost the same potency of MDMA, but it does not produce the same effects." He also stated that it "has an almost antidepressant action, pleasant and positive, but not the unique magic of MDMA." The toxicity of methylone has not been well-studied, although it likely does not exceed that of MDMA, and it has a limited history of human usage.

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/psychonautwiki.php'><img src='/images/psychonautwiki.gif' alt='psychonautwiki.org' title='psychonautwiki.org' class='logo'></a>
<div class='talllink'>Methylone Psychonaut Wiki: <br><a href='https://psychonautwiki.org/wiki/Methylone'>
https://psychonautwiki.org/wiki/Methylone</a>
</div></div>

<p>
<b>Similar to Ecstasy:</b><br>
The designer drug 3, 4-methylenedioxymethcathinone, commonly known as methylone, is often found in the substances labeled as "bath salts." The chemical composition of methylone is very similar to the structure of <a href='https://www.nonpsychotoxic.com/substances/mdma.php'>MDMA</a> (3, 4-methylenedioxymethamphetamine), and methylone is sometimes sold as Molly, suggesting that dealers are trying to pass it off as a substitute for ecstasy or similar drugs. Other street names for methylone include bubbles, explosion, MDMCAT, and ease. A number of research reports suggest that methylone use produces effects similar to MDMA and amphetamine. While the drug is a Schedule I controlled substance, it appears that its effects are not as well known as its use is not as extensive as similar drugs, even though the drug has been on the market for decades; it was originally developed in 1996 as a potential treatment for depression. Anecdotal evidence online from individuals claiming to have used the substance suggests that its effects can be somewhat varied and that its use is associated with a significant "crash" once the individual has stopped using the drug and its effects have begun to wear off.

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/americanaddictioncenters.php'><img src='/images/americanaddictioncenters.gif' alt='American Addiction Centers' title='American Addiction Centers' class='logo'></a>
<div class='talllink'>
Methylone Abuse: Dangers, Symptoms, and Treatment: <br><a href='https://americanaddictioncenters.org/bath-salts-abuse/methylone'>
https://americanaddictioncenters.org/bath-salts-abuse/methylone</a>
</div></div>

<p>
<b>Street Names:</b><br>
Meph, MC, MCAT, M-Cat, 4-MMC, Miaow, Meow Meow, Bubbles, Bounce, Charge, Drone, White Magic, Marzipan, Methylone

<p><b>Effects:</b><br>
Often described as a mix between Amphetamines, Ecstasy and Cocaine.  Users feel alert, confident, euphoric and talkative, and some feel greater empathy with those around them.  The effects last about an hour, but this can vary.

<p><b>Drug form and method of use:</b><br>
A fine white, off-white or yellowish powder - usually snorted like Cocaine or swallowed 'bombed' in wraps of paper.  Can be smoked and in rare cases is injected.  Also comes in capsules and pills.

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/ascert.php'><img src='/images/ascert.gif' alt='ASCERT' title='ASCERT' class='logo'></a>
<div class='link'>
Methylone (Cathinones): <br><a href='https://www.ascert.biz/drug-and-alcohol-information/a-z-drugs/methylone-cathinones/'>
https://www.ascert.biz/drug-and-alcohol-information/a-z-drugs/methylone-cathinones/</a>
</div></div>

<p>
<b>History:</b><br>

The drug methylone first made an appearance in 2004 under the name 'Explosion' in a number of smart shops in the Netherlands. The product was advertised as a 'room odorizer' containing 5ml of the liquid drug. 

When the new product was first introduced, there was much confusion over what each bottle contained. It was not until January 2005 that the contents of 'explosion' was analysed. In March 2005 there was only one manufacturer and therefore this one sample analysis came to represent all 'Explosion' bottles, despite any further quantitative and confirmative data.

 The new drug gained a great amount of popularity after the Dutch radio presenter Giel Beelen took the drug during a live show.

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/release.php'><img src='/images/release.gif' alt='Release' title='Release' class='logo'></a>
<div class='link'>
Methylone (Cathinones): <br><a href='https://www.release.org.uk/drugs/methylone/history'>
https://www.release.org.uk/drugs/methylone/history</a>
</div></div>

<p>
<table class='tripsit'>
<caption>Methylone </caption>
<thead><tr><td colspan = '4'><b>Duration:</b><br>
<p class='eat'>bk-MDMA is a cathinone stimulant and empathogen, similar in structure to <a href='https://www.nonpsychotoxic.com/substances/mdma.php'>MDMA</a>, though more stimulating and less empathogenic in comparison. Was very commonly mis-sold as MDMA on the street until it was banned in 2013. The Marquis reagent can differentiate bk-MDMA from MDMA. Less potent than MDMA with a slightly shorter duration.</p></td></tr>
<tr><th style='text-align: left;'>
<b>Route</b></th><th>Onset</th><th>Duration</th><th style='text-align: right;'>After Effects</th></tr></thead>
<tfoot><tr><th colspan = '4'>Tripsit Factsheets</th></tr>
<tr><td colspan='4'>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/tripsit.php'><img src='/images/tripsit.gif' alt='Tripsit Factsheets' title='Tripsit Factsheets' class='logo'></a>
<div class='link'>Methylone Basic Information: <br><a href='http://drugs.tripsit.me/methylone'>
http://drugs.tripsit.me/methylone</a>
</div></div>
</td></tr></tfoot>
<tbody>
<tr><td style='text-align: left;'><b>All ROAs:</b></td><td>15-60 minutes</td><td>2-4 hours</td><td style='text-align: right;'>6-24 hours</td></tr>
<tr><td colspan = '4'><img src='/images/methylone-duration-tripsit.gif' alt='Methylone Duration' class='tripsit'>
</td></tr><tr><th colspan = '4'><b>Marquis:</b><br>
Yellow 
</th></tr></tbody></table>

<p>
<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/njnQgxPZlqo" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <br>

<p>
<blockquote class='who'>
<b style='color: #d86422'>World Health Organization 2014:</b><br>
Methylone ((3,4-methylenedioxy)methcathinone) is a synthetic cathinone. It is the beta-keto version of 3,4-methylenedioxymethylamphetamine (<a href='https://www.nonpsychotoxic.com/substances/mdma.php'>mdma</a>). It was originally developed as a therapeutic for Parkinson's disease or depression by Shulgin. Use of methylone was first reported around 2005. Use/abuse has been reported from Japan, the USA and Europe. The effects and the mode of use reported have similarities with mdma, but its potency is less. <p class='who'>Reported toxic effects of methylone include tachycardia, hypertension, paranoia, anxiety, bruxism and muscle tension and aching. Some of these effects leeding to hospital admissions. A number of analytically confirmed drug-related deaths have been reported.</p>
Animal studies have indicated that methylone possesses an abuse or dependence potential but there are no human clinical data to support this. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/who.php'><img src='/images/who.gif' alt='World Health Organization' title='World Health Organization' class='logo'></a>
<a href='https://www.who.int/medicines/areas/quality_safety/4_14_Review.pdf'><img src='/images/methylone-who-pdf.png' alt='WHO PDF Methylone' class='pdf'></a>
<div class='pdflink'>Methylone (bk&#8208;MDMA) Critical Review Report (PDF 24 pages): <br><a href='https://www.who.int/medicines/areas/quality_safety/4_14_Review.pdf'>
https://www.who.int/medicines/areas/quality_safety/4_14_Review.pdf</a>
</div></div>
</blockquote>


<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/reddit.php'><img src='/images/reddit.gif' alt='Reddit' title='Reddit' class='logo'></a>
<div class='link'>Methylone Reddit Search Results: <br><a href='https://www.reddit.com/search/?q=methylone'>
https://www.reddit.com/search/?q=methylone</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/bluelight.php'><img src='/images/bluelight.gif' alt='Bluelight Forum' title='Bluelight Forum' class='logo'></a>
<div class='link'>The Big & Dandy bk-MDMA (Methylone) Thread (1000 comments): <br>
https://www.bluelight.org/xf/threads/the-big-dandy-bk-mdma-methylone-thread.299732/
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugs-forum.php'><img src='/images/drugs-forum.gif' alt='drugs-forum.com' title='drugs-forum.com' class='logo'></a>
<div class='link'>Tags - Methylone: <br><a href='https://drugs-forum.com/tags/methylone/'>
https://drugs-forum.com/tags/methylone/</a>
</div></div>




<p>
<div class='source'><a href='https://erowid.org/experiences/subs/exp_Methylone.shtml'><img src='/images/erowid.gif' alt='Erowid Experience Vaults' title='Erowid Experience Vaults' class='logo'></a>
<div class='link'>Erowid Experience Vault: <br><a href='https://erowid.org/experiences/subs/exp_Methylone.shtml'>
https://erowid.org/experiences/subs/exp_Methylone.shtml</a>
</div></div>
<p>


<div class='source'><img src='/images/blank.gif' alt='' title='' class='logo'></a>
<div class='link'>
Methylone and me: <br><a href='https://www.methylone.com/experiences/'>
https://www.methylone.com/experiences/</a>
</div></div>



<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/caymanchemical.php'><img src='/images/caymanchemical.gif' alt='Cayman Chemical' title='Cayman Chemical' class='logo'></a>
<a href='https://www.caymanchem.com/msdss/10986m.pdf'><img src='/images/methylone-caymanchem-pdf.png' alt='Caymanchem PDF Methylone' class='pdf'></a>
<div class='tallpdflink'>Methylone (hydrochloride) Safety Data Sheet (PDF 5 pages): <br><a href='https://www.caymanchem.com/msdss/10986m.pdf'>
https://www.caymanchem.com/msdss/10986m.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/swgdrug.php'><img src='/images/swgdrug.gif' alt='Science Working Group' title='Science Working Group' class='logo'></a>
<a href='https://www.swgdrug.org/Monographs/Methylone.pdf'><img src='/images/methylone-swgdrug-pdf.png' alt='SWGDRUG PDF Methylone' class='pdf'></a>
<div class='pdflink'>Methylone Monograph (PDF 4 pages): <br><a href='http://www.swgdrug.org/Monographs/Methylone.pdf'>
http://www.swgdrug.org/Monographs/Methylone.pdf</a>
</div></div>

<p>
<blockquote class='wikipedia'>
"Methylone" is also a trademarked brand name for an injectable form of methylprednisolone, a corticosteroid hormone used to treat arthritis and severe allergic reactions; hence, methylone may be confused with it. Aside from context, they can be distinguished by the fact that the name will usually be capitalized when referring to the prescription drug.
 A proposed alternate name is Bk-MDMA, or beta-keto-MDMA. While this nomenclature has not caught on because the name "methylone" became widely used before the conflicting Methylone trademark was noticed, the analogous names for related chemicals &#946;k-MDEA and &#946;k-MBDB have become the established names for those substances. 
</blockquote>
]]></description>
	<link>https://www.nonpsychotoxic.com/substances/methylone.php</link>
</item>

<item>
	<title></title>
	<pubDate>Tue, 15 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/methoxyamphetamine.php</guid>
	<description><![CDATA[<p>
<b>What is PMA?</b><br>
PMA is a methoxylated phenethylamine derivative. It is related in chemical structure and pharmacological properties to <a href='https://www.nonpsychotoxic.com/substances/mda.php'>methylenedioxyamphetamine (MDA)</a>, <a href='https://www.nonpsychotoxic.com/substances/mdma.php'>methylenedioxymethylamphetamine (MDMA)</a>, <a href='https://www.nonpsychotoxic.com/substances/n-ethyl-mda.php'>methy-lenedioxyethylamphetamine (MDEA)</a>, and <a href='https://www.nonpsychotoxic.com/substances/mescaline.php'>mescaline</a>. Although often sold as 'ecstasy', PMA is structurally most similar to mescaline and subsequently has strong hallucinogenic properties.
<p>
PMA was first encountered in the illegal drug market in the 1970s. Within a few years, PMA had been associated with several fatalities in Canada and subsequently earned the street name 'death'. PMA resurfaced in the 1990s in Australia and was again associated with a number of fatalities, particularly in South Australia. These deaths primarily occurred amongst people who thought they were consuming ecstasy.
<p>
PMA is also known as: 4-methoxyamphetamine, 4-MA, 'death', 'Dr Death'. Pure PMA is a white powder, but forms found on the street can also be beige, pink, or yellowish. It may knowingly be used on its own in order to increase the effects of MDMA; however, more often than not, PMA is sold as 'ecstasy' in either pill or capsule form. In these cases, it comes in a variety of different colours and with a variety of different logos, and is usually indistinguishable from ecstasy. This can be extremely dangerous since PMA has a higher potency (i.e. effects at lower doses) and a more delayed onset of activity than MDMA, and as such it is easier to overdose on PMA. High dosages of PMA can lead to sudden, large and potentially fatal increases in blood temperature, body temperature and blood pressure.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/ndarc.php'><img src='/images/ndarc.gif' alt='UNSW Australia National Drug and Alcohol Research Center' title='UNSW Australia National Drug and Alcohol Research Center' class='logo'></a>
<a href='https://ndarc.med.unsw.edu.au/sites/default/files/ndarc/resources/NDA073%20Fact%20Sheet%20PMA.pdf'><img src='/images/pma-ndarc-pdf.png' alt='NDARC PDF PMA' class='pdf'></a>
<div class='pdflink'>Paramethoxyamphetamine (PMA) Fact Sheet (PDF 1 page): <br><a href='https://ndarc.med.unsw.edu.au/sites/default/files/ndarc/resources/NDA073%20Fact%20Sheet%20PMA.pdf'>
https://ndarc.med.unsw.edu.au/sites/default/files/ndarc/resources/NDA073%20Fact%20Sheet%20PMA.pdf</a>
</div></div>

<p>
<b>What it looks like:</b><br>
PMA is sold as a pill but the pills can be lots of different colours and can have different marks on them. It is relatively easy to grind down pills to recolor and re-brand them with a new logo or design, so a pink heart-shaped pill can be made into a green round pill or a yellow square pill. As with any pill you can never be sure what it contains or how this might affect you.

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/knowthescore.php'><img src='/images/knowthescore.gif' alt='knowthescore.info' title='knowthescore.info' class='logo'></a>
<div class='talllink'>Scottish PMA Facts: <br><a href='https://knowthescore.info/drugs-a-z/pma/'>
https://knowthescore.info/drugs-a-z/pma/</a>
</div></div>


<p>
<b>PMA: not just another drug scare story:</b><br>
PMA - the common name for paramethoxyamphetamine - is usually sold in pill form, sometimes stamped with a crown, or M and sometimes pink (hence the nickname "pink ecstasy"). People who take PMA often believe they are taking ecstasy. The drug's effects are similar but they can take up to an hour to be felt, so users may take another pill in the mistaken belief that the first has not worked, resulting in a massive dose.
<p>
"PMA is a potent releaser of serotonin," says Sumnall. "It also prevents the reuptake of serotonin back into neurons and inhibits the enzymes which are responsible for the breakdown of serotonin. This increase in serotonin, especially when PMA is taken in combination with other drugs, can lead to hyperthermia and subsequently, organ failure. Basically people are overheating and collapsing."

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/theguardian.php'><img src='/images/theguardian.gif' alt='The Guardian' title='The Guardian' class='logo'></a>
<div class='link'>PMA: not just another drug scare story (2013): <br><a href='https://www.theguardian.com/society/shortcuts/2013/jul/22/pma-not-another-drug-scare-story'>
https://www.theguardian.com/society/shortcuts/2013/jul/22/pma-not-another-drug-scare-story</a>
</div></div>

<p>
<b>Dr Death is often mistaken for ecstasy, but is more lethal:</b><br>
Dr Death is also known as Pink Mitsubishi, PMA, Pink McDonalds, Pink Ecstasy, Killer, and Chicken Fever. The drug was first synthesised in 1967 by the psychedelic chemist Alexander Shulgin, the so-called godfather of <a href='https://www.nonpsychotoxic.com/substances/mdma.php'>MDMA</a>. At the time he advised people to beware of the compound, according to Mike Power, author of Drugs 2.0. The drug is believed to have been first identified in the United States in the early 1970s.
<p><b>What are its effects?</b><br>

The drug has a similar high to MDMA, and can have psychedelic properties. It gives the user a buzz which makes sounds and colours feel more intense. It can also make a person feel like they have an intense affinity with those around them. But while Ecstasy can kick in after 20 minutes, it can take PMA up to an hour to begin working - sometimes leading people to fatally up their dose.

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/independent.php'><img src='/images/independent.gif' alt='independent.co.uk' title='independent.co.uk' class='logo'></a>
<div class='link'>Dr Death is often mistaken for ecstasy, but is more lethal (2014): <br><a href='https://www.independent.co.uk/life-style/health-and-families/health-news/dr-death-what-is-new-party-drug-and-what-are-the-risks-9644008.html'>
https://www.independent.co.uk/life-style/health-and-families/health-news/dr-death-what-is-new-party-drug-and-what-are-the-risks-9644008.html</a>
</div></div>

<p>
<b>Effects of PMA and PMMA:</b><br>

There is no safe level of drug use. Use of any drug always carries some risk. It's important to be careful when taking any kind type of drug.
<p>
PMA and PMMA affect everyone differently, but effects may include:
<ul><li>Moderate stimulation</li><li>Seeing colours and shapes</li><li>Heightened senses (sight, hearing and touch)</li><li>Dizziness</li><li>Dry mouth and dehydration</li><li>Increased bodily temperature - <b>The most common cause of death from PMA is due to severe hyperthermia</b></li><li>Increased perspiration teeth grinding</li><li>Increased sweating</li><li>Increased heartbeat and blood pressure</li><li>Difficulty breathing</li><li>Irregular eye movements</li><li>Muscle spasms</li><li>Decreased appetite</li><li>Nausea and vomiting (common at any dose)</li><li>Seizures - (more common with PMMA than with almost any other substance)</LI></UL>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/adf.php'><img src='/images/adf.gif' alt='Austrailia Alcohol and Drug Foundation' title='Austrailia Alcohol and Drug Foundation' class='logo'></a>
<div class='link'>PMA and PMMA?: <br><a href='https://adf.org.au/drug-facts/pma-and-pmma/'>
https://adf.org.au/drug-facts/pma-and-pmma/</a>
</div></div>

<p class='update'>
PMA can cause life-threatening side effects (such as hyperthermia and serotonin syndrome) even at moderate doses. As a result, using this substance is strongly discouraged. It is also advised to always test your MDMA for the presence of PMA using a <a href='https://www.google.com/search?q=reagent+testing+kit'>reagent testing kit</a> as it is a common adulterant.
</p>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/psychonautwiki.php'><img src='/images/psychonautwiki.gif' alt='psychonautwiki.org' title='psychonautwiki.org' class='logo'></a>
<div class='talllink'>PMA Summary Sheet: <br><a href='https://psychonautwiki.org/wiki/PMA'>
https://psychonautwiki.org/wiki/PMA</a>
</div></div>



<p>
<b>Addictive:</b><br>
As with ecstasy, it's possible to build up a tolerance (which means people need to take more PMA to get the same level of buzz). Psychological dependence may also develop (with an increased desire to keep taking the drug despite the risks). There have been no clear physical withdrawals reported with PMA but, as with ecstasy, users may feel lethargic or low for some days after having used.
<p>
<b>How long does it stay in your system?</b><br>
Shows up in urine tests for 3-8 days. (The length of time depends on the test used, the amount you take, if you have other medical conditions and your own metabolism. Please use this figure as a guide only).
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugsie.php'><img src='/images/drugsie.gif' alt='drugs.ie' title='drugs.ie' class='logo'></a>
<div class='link'>PMA: <br><a href='http://www.drugs.ie/drugtypes/drug/pma'>
http://www.drugs.ie/drugtypes/drug/pma</a>
</div></div>

<p>
<blockquote class='emcdda'>
<b>EMCDDA - Europol Joint Report 2012:</b><br>
<ul><li>Twelve Member States as well as Croatia and Norway reported to Europol and the EMCDDA seizures of 4-methylamphetamine mostly in powder or paste form, ranging from 0.02 g up to 147 kg. A few seizures were in tablet or liquid form.
</li><li>Samples that contained 4-methylamphetamine typically contained amphetamine and caffeine in varying ratios.
</li><li>According to information provided to Europol, in recent years multiple illicit production sites and/or other indications related to the production of 4-methylamphetamine have been discovered in the Netherlands. Seizures related to international trafficking of 4-methylamphetamine have been reported by two Member States with indications of trafficking from a third Member State.
</li><li>According to information provided to Europol no distinct difference can be made between 4-methylamphetamine and <a href='https://www.nonpsychotoxic.com/substances/amphetamine.php'>amphetamine</a> in terms of the involvement of organised crime groups, production, trade, and/or users. 
</li><li>There is little evidence to suggest a specific demand for 4-methylamphetamine. However, the substance is sold as amphetamine (e.g. as 'speed'). Drug prevalence estimates suggest that about 12.5 million Europeans have tried amphetamines, and about 2 million have used the drug during the last year. Consequently, this population may be at risk of exposure to 4-methylamphetamine if this substance becomes more widely available.
</li><li>4-methylamphetamine has no known medical use (human or veterinary) in the European Union. </li></ul>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/europol.php'><img src='/images/europol.gif' alt='Europol' title='Europol' height='30'></a><br><a href='https://www.nonpsychotoxic.com/sources/emcdda.php'><img src='/images/emcdda.gif' alt='European Monitoring Centre for Drugs and Drug Addiction' title='European Monitoring Centre for Drugs and Drug Addiction' class='logo'></a>
<a href='https://www.emcdda.europa.eu/system/files/publications/749/TDAS12001ENN_400433.PDF'><img src='/images/4-ma-emcdda.png' alt='4-MA Joint Report' class='pdf'></a>
<div class='tallpdflink'>4-MA Joint Reports (PDF 40 pages): <br><a href='https://www.emcdda.europa.eu/system/files/publications/749/TDAS12001ENN_400433.PDF'>
https://www.emcdda.europa.eu/system/files/publications/749/TDAS12001ENN_400433.PDF</a><br>
</div></div>
</blockquote>


<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/erowid.php'><img src='/images/erowid.gif' alt='Erowid Experience Vaults' title='Erowid Experience Vaults' class='logo'></a>
<div class='link'>PMA Experience Reports: <br><a href='https://www.erowid.org/experiences/subs/exp_PMA.shtml'>
https://www.erowid.org/experiences/subs/exp_PMA.shtml</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/swgdrug.php'><img src='/images/swgdrug.gif' alt='Science Working Group' title='Science Working Group' class='logo'></a>
<a href='https://www.swgdrug.org/Monographs/p-METHOXYAMPHETAMINE.pdf'><img src='/images/pma-swgdrugc-pdf.png' alt='SWGDRUG PDF PMA' class='pdf'></a>
<div class='pdflink'>p-Methoxyamphetamine (PMA) Monograph (PDF 12 pages): <br><a href='http://www.swgdrug.org/Monographs/p-METHOXYAMPHETAMINE.pdf'>
http://www.swgdrug.org/Monographs/p-METHOXYAMPHETAMINE.pdf</a>
</div></div>


<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/caymanchemical.php'><img src='/images/caymanchemical.gif' alt='Cayman Chemical' title='Cayman Chemical' class='logo'></a>
<a href='https://www.caymanchem.com/msdss/12041m.pdf'><img src='/images/4-methoxyamphetamine-caymanchem-pdf.png' alt='Caymanchem PDF 4-Methoxyamphetamine' class='pdf'></a>
<div class='tallpdflink'>4-Methoxyamphetamine (hydrochloride) Safety Data Sheet (PDF 5 pages): <br><a href='https://www.caymanchem.com/msdss/12041m.pdf'>
https://www.caymanchem.com/msdss/12041m.pdf</a>
</div></div>

<p>
<blockquote class='dgidb'>
<b>Alternate Names:</b><br>
para-Methoxyamphetamine, 
beta-methoxyamphetamine
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/dgidb.php'><img src='/images/dgidb.gif' alt='The Drug Gene Interaction Database' title='The Drug Gene Interaction Database' class='logo'></a>
<div class='link'>para-Methoxyamphetamine Drug Record: <br><a href='http://www.dgidb.org/drugs/PARA-METHOXYAMPHETAMINE'>
http://www.dgidb.org/drugs/PARA-METHOXYAMPHETAMINE</a>
</div></div>
</blockquote>



<p>
<blockquote class='wikipedia'>
Effects of PMA ingestion include many effects of the hallucinogenic amphetamines including accelerated and irregular heartbeat, blurred vision, and a strong feeling of intoxication that is often unpleasant. At high doses unpleasant effects such as nausea and vomiting, severe hyperthermia and hallucinations may occur. The effects of PMA also seem to be much more unpredictable and variable between individuals than those of MDMA, and sensitive individuals may die from a dose of PMA that a less susceptible person might only be mildly affected by. While PMA alone may cause significant toxicity, the combination of PMA with MDMA has a synergistic effect that seems to be particularly hazardous.
</blockquote>
]]></description>
	<link>https://www.nonpsychotoxic.com/substances/methoxyamphetamine.php</link>
</item>

<item>
	<title></title>
	<pubDate>Mon, 14 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/marihuana.php</guid>
	<description><![CDATA[<div class='container' style='max-width: 900px;'>
   <img src='/images/marijuana-campusdrugprevention.jpg' alt='Marijuana'>
  <div class='containerbottom'><p>Marijuana</p></div>
</div>

<p>
Marijuana refers to the dried leaves, flowers, stems, and seeds from the Cannabis sativa or Cannabis indica plant. The plant contains the mind-altering chemical THC and other related compounds. People use marijuana by smoking, eating, drinking, or inhaling it. Smoking and vaping THC-rich extracts from the marijuana plant (a practice called dabbing) is on the rise.
<p>
THC overactivates certain brain cell receptors, resulting in effects such as:
<ul>
 <li>Altered senses</li>
 <li>Changes in mood</li>
 <li>Impaired body movement</li>
 <li>Difficulty with thinking and problem-solving</li>
 <li>Impaired memory and learning</li>
</ul>
<p>
Marijuana use can have a wide range of health effects, including:
<ul>
 <li>Hallucinations and paranoia</li>
 <li>Breathing problems</li>
 <li>Possible harm to a fetus's brain in pregnant women</li>
</ul>
<p>
The amount of THC in marijuana has been increasing steadily in recent decades, creating more harmful effects in some people. It's unlikely that a person will fail a drug test or get high from passive exposure by inhaling secondhand marijuana smoke. There aren't any reports of teens and adults dying from using marijuana alone, but marijuana use can cause some very uncomfortable side effects, such as anxiety and paranoia and, in rare cases, extreme psychotic reactions. Marijuana use can lead to a substance use disorder, which can develop into an addiction in severe cases. No medications are currently available to treat marijuana use disorder, but behavioral support can be effective.
<p class='update'>
Marijuana is the most commonly used illicit drug in the United States.
</p>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugabuse.php'><img src='/images/drugfacts.gif' alt='Drugabuse.gov' title='drugabuse.gov' class='logo'></a>
<div class='link'>Excerpt from <a href='https://www.drugabuse.gov/publications/drugfacts/marijuana'>https://www.drugabuse.gov/publications/drugfacts/marijuana</a>
</div></div>

<p>
The term 'marijuana' (sometimes spelled 'marihuana') is Mexican in origin and typically refers to any part of - or any one of - the three distinctive subspecies of the cannabis plant: cannabis sativa (which tends to grow tall and stalky), cannabis indica (which tends to grow smaller and bushier), or cannabis ruderalis (found primarily in Russia and Eastern Europe.) Marijuana is the third most popular recreational drug in America (behind only alcohol and tobacco), and has been used by nearly 100 million Americans. According to government surveys, some 25 million Americans have smoked marijuana in the past year, and more than 14 million do so regularly despite laws against its use.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/norml.php'><img src='/images/norml.gif' alt='National Organization for the Reform of Marijuana Laws' title='National Organization for the Reform of Marijuana Laws' class='logo'></a>
<div class='link'>About Marijuana: <br><a href='https://norml.org/aboutmarijuana'>
https://norml.org/aboutmarijuana</a>
</div></div>

<p>
<b>Legality (December 2020):</b><br>
<p><img src='/images/marijuana-states-mpp.gif' alt='Marijuana State Policy Map mpp.org' class='center'>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/mpp.php'><img src='/images/mpp.gif' alt='Marijuana Policy Project' title='Marijuana Policy Project' class='logo'></a>
<div class='talllink'>Select Your State Here: <br><a href='https://www.mpp.org/states/'>
https://www.mpp.org/states/</a>
</div></div>

<p>
<img src='/images/marijuana-testing-questdiagnostics.gif' alt='US Marijuana Drug Testing Psoitivity' class='center'><br>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/questdiagnostics.php'><img src='/images/questdiagnostics.gif' alt='Quest Diagnostics' title='Quest Diagnostics' class='logo'></a>
<div class='link'>Map of the U.S. depicting Marijuana positivity: <br><a href='https://www.questdiagnostics.com/home/physicians/health-trends/drug-testing/map_marijuana/'>
https://www.questdiagnostics.com/home/physicians/health-trends/drug-testing/map_marijuana/</a>
</div></div>

<p>
<b>Why spelled with an H:</b><br>
So why does Michigan (and Cannabis Attorneys of Michigan) spell marihuana with an "h" anyway?  Michigan's spelling is primarily sourced from the original spelling of the word, which first appears in US law in the Marihuana Tax Act of 1937, drafted by the infamous Harry Anslinger, head of the Bureau of Narcotics under FDR.  Its origins are in , Mexican-Spanish, and the later modern spelling using a "j" was an uniquely American one.  Canada spells it with an "h" as well, as does the federal government on occasion.  Our firm uses the "h" spelling out of deference to the Michigan spelling.  Both "j" and "h" spellings are equally accurate and acceptable, but if you are conflicted, you can always just use "cannabis".<p>
<div class='source'><img src='/images/blank.gif' alt='' title='' height='30' class='logo'>
<div class='link'>- <a href='https://www.cannabisattorneysofmichigan.com/marihuana-with-an-h/'>https://www.cannabisattorneysofmichigan.com/marihuana-with-an-h/</a>
</div></div>

<p>
<b>Edibles:</b><br>
Food products infused with marijuana. Though smoking marijuana is the most prevalent method of consumption, eating marijuana is quickly becoming a popular way to consume the drug. Brownies are among the most common food products infused with marijuana, however, almost any food product may be infused with marijuana and eaten. In addition to placing marijuana directly in food, marijuana-infused cooking oil can be used when frying or searing food, and marijuana-infused butter can be spread directly on prepared food. These marijuana edibles are more common in states that have legalized marijuana and also states that permit medical marijuana use.
<p>
The effects from smoking marijuana only takes minutes. Edibles, however, take between 1-3 hours because food is absorbed into the bloodstream through the liver. Because it takes longer, the user may end up consuming longer amounts of the drug while thinking the drug isn't working. The amount of THC, the active ingredient in marijuana, is very difficult to measure and is often unknown in these food products. If the user has other medications in his or her system, their body may metabolize different amounts of THC, causing THC levels in the bloodstream to dangerously increase five-fold.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/justthinktwice.php'><img src='/images/justthinktwice.gif' alt='Drug Enforcement Administration Website Just Think Twice' title='Drug Enforcement Administration Website Just Think Twice' class='logo'></a>
<div class='talllink'>Drug Alert: Marijuana Edibles: <br><a href='https://www.justthinktwice.gov/article/drug-alert-marijuana-edibles'>
https://www.justthinktwice.gov/article/drug-alert-marijuana-edibles</a>
</div></div>

<p>
<b>Marijuana in the Body:</b><br>
When marijuana is smoked, it travels down the windpipe and into the lungs. Once in the lungs, the smoke passes through the bronchi and into the alveoli (air sacs) where the THC passes into the bloodstream. THC is then absorbed by most tissues and organs in the body, especially fat cells and organs such as the brain. The "high" reaches its peak in approximately 10-30 minutes and will last from two to eight hours, depending on the amount of marijuana used. It takes a week to one month for all the chemicals from one marijuana cigarette to leave the body. As more marijuana is smoked, THC accumulates in the cells and the body is never drug free. When chronic users stop using marijuana, it takes about three months for the accumulation of THC to leave the body. When marijuana is eaten, it enters the stomach and is broken down for digestion by enzymes. At this time, THC passes into the bloodstream. Smoking marijuana puts 5-10 times more THC into the body than eating it.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/gmu.php'><img src='/images/gmu.gif' alt='George Mason University' title='George Mason University' class='logo'></a>
<div class='talllink'>What is Marijuana: <br><a href='http://www.gmu.edu/resources/facstaff/facultyfacts/1-2/grass.html'>
http://www.gmu.edu/resources/facstaff/facultyfacts/1-2/grass.html</a>
</div></div>

<p>
<b>Endocannabinoids and What They Do:</b><br>
To understand what marijuana does to a user in the long run, it's necessary to look at how the drug works in the brain. Marijuana is as effective as it is because its active chemical compound (tetrahydrocannabinol, or THC) mimics substances called endocannabinoids that the human body produces on its own. In the brain, endocannabinoids work by controlling the production of neurotransmitters (chemical substances that facilitate communication between the brain and the central nervous system). In the rest of the body, endocannabinoids relax muscles, reduce inflammation, protect damaged tissue, and regulate appetite and metabolism, among many other functions. Because endocannabinoids are so important, the brain has readymade receptors for them. Since the THC in cannabis mimics natural endocannabinoids, marijuana is unique among other drugs in that regard. The same physiological effects that arise from the normal application of endocannabinoids are triggered with the use of marijuana, especially in the brain. This is why smokers experience memory issues, augmented levels of pain, and alterations to emotion, pleasure, and movement control.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/americanaddictioncenters.php'><img src='/images/americanaddictioncenters.gif' alt='American Addiction Centers' title='American Addiction Centers' class='logo'></a>
<div class='talllink'>Dangers of Marijuana: Long-Term Effects of Pot on the Brain and Body: <br><a href='https://americanaddictioncenters.org/marijuana-rehab/long-term-effects'>
https://americanaddictioncenters.org/marijuana-rehab/long-term-effects</a>
</div></div>

<p>
<b>History:</b><br>
Marijuana is the slang term for portions of the Cannabis plant which has three species: Cannabis sativa; Cannabis indica and Cannabis ruderalis. The flowering plant, which can grow to 16 feet (5 meters) high, likely originated in the Central Asian steppe, near the Altai or Tian Shian Mountains, and was first cultivated in China and India. It is one of the oldest psychoactive substances used by man. The leaves, stems, flower buds and extracts from the marijuana plant can be eaten, brewed in a tea or put into a tincture. It can also be vaporized using an e-cigarette pen. There are hundreds of compounds in marijuana, but scientists believe the one responsible for the drugs' psychoactive effects is <a href='https://www.nonpsychotoxic.com/substances/tetrahydrocannabinols.php'>tetrahydrocannbinol, or THC</a>. THC binds to cannabinoid receptors throughout the body, and marijuana's "high" comes from THC's binding to brain regions responsible for pleasure, time perception, and pain. This binding in turn triggers a chemical cascade that eventually stimulates the production of dopamine, a brain chemical often called the "feel good chemical," which is part of the body's reward system. Subjective effects really vary," Earleywine said. "Folks who like it emphasize the euphoria and the relaxation, and then depending on the strain, it's mildly stimulating, or mildly sedating. 
<p>
<b>Ancient History:</b><br>
A 10,000-year-old archaeological site in Taiwan contains pottery fragments with a twisted strand imprinted around the edge, which some believe was made by pressing a rope made of hemp, the fibers made from the cannabis plant, across the wet clay. Hemp fabric was widely used in ancient China to make clothing. A Chinese medicinal textbook, the Pen Ts'ao, which is credited to an emperor in 2800 B.C., claims that "Ma," or marijuana, was a powerful medicinal plant. Siberian burial mounds have traces of burnt cannabis seeds dating to 3000 B.C. The plant was first given its taxonomic identification by Carl Linnaeus in 1753 and thoroughly described to Westerners in the 1800s, when the medical doctor William O'Shaughnessy gave a report to the Medical and Physical Society of Calcutta in India in 1839. The doctor described its effects on people and did a few case reports on "gunjah," the Indian name for the drug. The drug first became popular in Europe when Napoleon's troops returned from Egypt.
<p>
<b>American History:</b><br>
In the Americas, Cannabis extract was a popular medicinal drug in the 1800s. But in the 1900s, the tide began to turn against the drug. In the 1920s, Mexican immigrants became associated with the smoked, recreational version of the drug, and anti-immigrant sentiments fueled marijuana prohibition. By the 1930s, marijuana was banned in 24 states. The newly minted Federal Bureau of Narcotics launched a campaign against the drug. By 1937, Congress passed the Marihuana Tax Act, which effectively banned marijuana except for a few medicinal purposes. In the 1950s, the Narcotics Control Act and the Boggs Act stiffened penalties for marijuana possession, with first-time offenses requiring two to 10 year sentences and a minimum $20,000 fine. Penalties were relaxed in the 1970s, but President Ronald Reagan increased federal penalties for marijuana possession in the 1980s. As of early 2017, 26 states and the District of Columbia have legalized pot in some form of medical and/or recreational use, with other states soon to follow.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/livescience.php'><img src='/images/livescience.gif' alt='Live Science' title='Live Science' class='logo'></a>
<div class='link'>Marijuana: Facts About Cannabis: <br><a href='https://www.livescience.com/24559-marijuana-facts-cannabis.html'>
https://www.livescience.com/24559-marijuana-facts-cannabis.html</a>
</div></div>

<p>
<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/0ygtX2nyexo" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <p>

<div class="youtube"> <iframe class="youtubeiframe" 
src="https://www.youtube.com/embed/VFwYGFt5q90" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>
</div> <br>

<p>
<b>NIH - Letter From the Director:</b><br>
Changes in marijuana policies across states legalizing marijuana for medical and/or recreational use suggest that marijuana is gaining greater acceptance in our society. Thus, it is particularly important for people to understand what is known about both the adverse health effects and the potential therapeutic benefits linked to marijuana. Because marijuana impairs short-term memory and judgment and distorts perception, it can impair performance in school or at work and make it dangerous to drive. It also affects brain systems that are still maturing through young adulthood, so regular use by teens may have negative and long-lasting effects on their cognitive development, putting them at a competitive disadvantage and possibly interfering with their well-being in other ways.  
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugabuse.php'><img src='/images/nihreport.gif' alt='NIH RePORT' title='NIH RePORT' class='logo'></a>
<div class='link'>Marijuana Research Report: <br><a href='https://www.drugabuse.gov/publications/research-reports/marijuana/letter-director'>
https://www.drugabuse.gov/publications/research-reports/marijuana/letter-director</a>
</div></div>

<p>
<b>Does Marijuana Help Treat Glaucoma?</b><br>
Cannabis and currently available compounds derived from marijuana - like <a href='https://www.nonpsychotoxic.com/cbd-explained.php'>CBD</a> - are not an adequate treatment for glaucoma, or any eye condition. To treat glaucoma, eye pressure must be managed 24 hours a day. Marijuana is not a practical treatment for constant use. And more research is still needed into the exact effects of cannabis and cannabis compounds on eye pressure and glaucoma. The American Academy of Ophthalmology does not recommend marijuana or other cannabis products for the treatment of glaucoma. The American Glaucoma Society and the Canadian Ophthalmological Society agree.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/aao.php'><img src='/images/aao.gif' alt='American Academy of Ophthalmology' title='American Academy of Ophthalmology' class='logo'></a>
<div class='link'>Does Marijuana Help Treat Glaucoma or Other Eye Conditions?<br><a href='https://www.aao.org/eye-health/tips-prevention/medical-marijuana-glaucoma-treament'>
https://www.aao.org/eye-health/tips-prevention/medical-marijuana-glaucoma-treament</a>
</div></div>

<p>
<b>Cannabis for Multiple Sclerosis?</b><br>
There have been numerous studies conducted to evaluate the effects of cannabinoids on MS-related pain, spasticity, and bladder symptoms. Most studies involved relatively small numbers of people with MS and the outcome measures varied among studies. However, reviews of published studies have generally shown that synthetic cannabinoids favorably impact symptoms of pain and spasticity. Less in known about the impact of inhaled or ingested botanical cannabis on MS symptoms. Based on existing evidence, cannabis products are probably effective for treating patient-reported symptoms of spasticity and pain. Based on existing evidence, cannabis is probably not effective for MS-related tremor or urinary incontinence. People with MS should be aware of potential adverse effects of cannabis products, including new or worsening cognitive symptoms, psychosis, tolerance and dependence, as well as drug-drug interactions. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/nationalmssociety.php'><img src='/images/nationalmssociety.gif' alt='National Multiple Sclerosis Society' title='National Multiple Sclerosis Society' class='logo'></a>
<a href='https://www.nationalmssociety.org/NationalMSSociety/media/MSNationalFiles/Professionals/Cannabis-and-Multiple-Sclerosis.pdf'><img src='/images/marijuana-nationalmssociety-pdf.png' alt='Nationalmssociety PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Cannabis for Multiple Sclerosis Symptoms (PDF 12 pages): <br><a href='https://www.nationalmssociety.org/NationalMSSociety/media/MSNationalFiles/Professionals/Cannabis-and-Multiple-Sclerosis.pdf'>
https://www.nationalmssociety.org/NationalMSSociety/media/MSNationalFiles/Professionals/Cannabis-and-Multiple-Sclerosis.pdf</a>
</div></div>

<p>
<b>Effects of Marijuana on the Lungs:</b><br>
Someone who smokes marijuana regularly may have many of the same respiratory problems that tobacco smokers have. These individuals may have a daily cough and phlegm, symptoms of chronic bronchitis, and more frequent chest colds. Continuing to smoke marijuana can lead to abnormal functioning of lung tissue injured or destroyed by marijuana smoke. Regardless of the THC content, the amount of tar inhaled by marijuana smokers and the level of carbon monoxide absorbed are three to five times greater than among tobacco smokers. This may be due to the marijuana users inhaling more deeply and holding the smoke in the lungs.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/narconon.php'><img src='/images/narconon.gif' alt='Narconon' title='Narconon' class='logo'></a>
<div class='talllink'>Marijuana Information: <br><a href='https://www.narconon.org/drug-information/marijuana-pot.html'>
https://www.narconon.org/drug-information/marijuana-pot.html</a>
</div></div>

<p>
<b>Smoking Marijuana and the Lungs:</b><br>
Despite marijuana's legalization in many states, it may be harmful to your health, particularly if you have lung disease or other medical conditions. The harmful effects of tobacco smoke are well known, but we have less information about the health effects of marijuana. Few research studies have been done since marijuana remains illegal in most countries, and since marijuana can be inhaled in many ways (e.g. water pipes, joints, vaping etc). It is likely that in frequent users (and some less frequent users), marijuana harms the lungs, and that there is not a safe way to smoke marijuana. Marijuana smoke may increase your risk of lung cancer. Marijuana smoke contains over 450 unique chemicals including many cancer-causing chemicals (carcinogens) similar to tobacco smoke. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/thoracic.php'><img src='/images/thoracic.gif' alt='American Thoracic Society' title='American Thoracic Society' class='logo'></a>
<a href='https://www.thoracic.org/patients/patient-resources/resources/marijuana.pdf'><img src='/images/marijuana-thoracic-pdf.png' alt='Thoracic PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Smoking Marijuana and the Lungs (PDF 2 pages): <br><a href='http://www.thoracic.org/patients/patient-resources/resources/marijuana.pdf'>
http://www.thoracic.org/patients/patient-resources/resources/marijuana.pdf</a>
</div></div>

<p>
<b>Top Ten Marijuana Myths:</b><br>
<div class='columns'>
<ol class='numbers'><li><div class='together'>Marijuana is harmless
</div></li><li><div class='together'>Marijuana is medicine
</div></li><li><div class='together'>The marijuana 'high' only lasts for a few hours
</div></li><li><div class='together'>Presence-in-system testing is unreliable because it does not measure impairment
</div></li><li><div class='together'>Marijuana is not addictive
</div></li><li><div class='together'>Marijuana can be regulated like alcohol
</div></li><li><div class='together'>Marijuana is not a gateway drug
</div></li><li><div class='together'>Marijuana is safer than cigarettes or alcohol
</div></li><li><div class='together'>There are no long-term effects from marijuana use
</div></li><li><div class='together'>It is safer to drive with marijuana in your system
</div></li></ol></div>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/datia.php'><img src='/images/datia.gif' alt='The Drug and Alcohol Testing Industry Association' title='The Drug and Alcohol Testing Industry Association' class='logo'></a>
<a href='https://www.dfaf.org/wp-content/uploads/2018/08/Busting-the-Top-10-Marijuana-Myths.pdf'><img src='/images/marijuana-datia-pdf.png' alt='DATIA PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Busting the Top Ten Marijuana Myths (PDF 2 pages): <br><a href='https://www.dfaf.org/wp-content/uploads/2018/08/Busting-the-Top-10-Marijuana-Myths.pdf'>
https://www.dfaf.org/wp-content/uploads/2018/08/Busting-the-Top-10-Marijuana-Myths.pdf</a>
</div></div>

<p>
<b>Marijuana and Alcohol:</b><br>
Marijuana is a depressant and a hallucinogen, which means that while it works to lower stress and anxiety, makes it harder to think straight, and interferes with memory and movement abilities. 
People commonly combine marijuana and alcohol, and as marijuana becomes legal for recreational purposes in many states, this practice is likely to increase. Both of these drugs have many similar effects, but act through different mechanisms. Both result in sedation, alterations in judgment, perceptual effects that include time distortions and even minor hallucinogenic effects, and physical effects that include slowed reflexes and decreased motor coordination.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/alcohol.php'><img src='/images/alcoholorg.gif' alt='alchohol.org' title='alchohol.org' class='logo'></a>
<div class='link'>Excerpt from alchohol.org: <br><a href='https://www.alcohol.org/mixing-with/marijuana/'>
https://www.alcohol.org/mixing-with/marijuana/</a>
</div></div>

<p>
<b>Addiction to Marijuana:</b><br>
When an individual uses marjiuana, cannabinoid receptors in the brain are activated by a neurotransmitter called Anandamide. THC mimics and blocks the actions natural neurotransmitters like Anandamide, to the point where the body no longer produces sufficient Anandamide on its own. The user's brain gets reprogrammed to need marijuana just to feel normal. When the user stops bringing more THC into the body, they often experience withdrawal symptoms because of the resulting lack of Anandamide. Wanting to quit using marijuana, but being unable to do so, is a strong indication of an addiction.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/addictioncenter.php'><img src='/images/addictioncenter.gif' alt='addictioncenter.com' title='addictioncenter.com' class='logo'></a>
<div class='link'>Addiction to Marijuana: <br><a href='https://www.addictioncenter.com/drugs/marijuana/'>
https://www.addictioncenter.com/drugs/marijuana/</a>
</div></div>

<p>
<b>Is Marijuana Addictive?</b><br>
Numerous research studies show that marijuana is indeed an addictive substance. The rate of addiction to marijuana has increased for all age groups. Teens are using the drug at younger ages. About one out of every six adolescents who use marijuana develop addiction to it, and half the people who receive treatment for marijuana use are under the age of 25. While the frequency of use seems to have remained the same over the past several years, adults are becoming dependent on marijuana more often. Theories about potential reasons for that increase include increased access to marijuana that is of higher potency, as well as a lower age at which many individuals first use this drug. The symptoms of marijuana withdrawal are similar to those of other drugs, especially tobacco. Those symptoms usually start one to two days after last using marijuana and include irritability, anger, depression, insomnia, drug craving, and decreased appetite.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/medicinenet.php'><img src='/images/medicinenet.gif' alt='medicinenet' title='medicinenet' class='logo'></a>
<div class='link'>Marijuana (Cannabis) facts: <br><a href='https://www.medicinenet.com/marijuana/article.htm'>
https://www.medicinenet.com/marijuana/article.htm</a>
</div></div>

<p>
<b>Marijuana and Teens:</b><br>
Many teenagers try marijuana and some use it regularly. Teenage marijuana use is at its highest level in 30 years, and today's teens are more likely to use marijuana than tobacco. Many states allow recreational use of marijuana in adults ages 21 and over. Recreational marijuana use by children and teenagers is not legal in anywhere in the United States. Today's marijuana plants are grown differently than in the past and can contain two to three times more <a href='https://www.nonpsychotoxic.com/substances/tetrahydrocannabinols.php'>tetrahydrocannabinol (THC)</a>, the ingredient that makes people high. Marijuana use in teens can lead to long-term consequences. Teens rarely think they will end up with problems related to marijuana use, so it is important to begin talking about the risks with your child early and continue this discussion over time. Talking with your child about marijuana can help delay the age of first use and help protect their brain. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/aacap.php'><img src='/images/aacap.gif' alt='American Academy of Child and Adolescent Psychiatry' title='American Academy of Child and Adolescent Psychiatry' class='logo'></a>
<div class='talllink'>Marijuana and Teens: <br><a href='https://www.aacap.org/AACAP/Families_and_Youth/Facts_for_Families/FFF-Guide/Marijuana-and-Teens-106.aspx'>
https://www.aacap.org/AACAP/Families_and_Youth/Facts_for_Families/FFF-Guide/Marijuana-and-Teens-106.aspx</a>
</div></div>

<p>
<b>Tips for Teens:</b>
<ul><li><b>Q.</b> Isn't smoking marijuana less dangerous than smoking cigarettes?<br>
<b>A.</b> No. It's even worse. Five joints a day can be as harmful as 20 cigarettes a day.
</li><li><b>Q.</b> Can people become addicted to marijuana?<br>
<b>A.</b> Yes. Research confirms you can become hooked on marijuana
</li><li>Marijuana affects your brain. THC (the active ingredient in marijuana) affects the nerve cells in the part of the brain where memories are formed.
</li><li>Know the risks.  Marijuana affects your coordination and reaction time, raising your risk of injury or death from car crashes and other accidents. In 2011, nearly 456,000 emergency room visits were related to marijuana use.
</li><li>Marijuana affects your lungs. Marijuana smoke deposits four times more tar in the lungs and contains 50 percent to 70 percent more cancer-causing substances than tobacco smoke does.
</li><li>Marijuana is not always what it seems. Marijuana can be laced with substances such as PCP, formaldehyde, or codeine cough syrup without your knowledge. "Blunts" - hollowed-out cigars filled with marijuana - sometimes have crack cocaine added.
</li></ul>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/samhsa.php'><img src='/images/samhsa.gif' alt='samhsa.gov' title='samhsa.gov' class='logo'></a>
<a href='https://store.samhsa.gov/system/files/phd641.pdf'><img src='/images/marijuana-samhsa-pdf.png' alt='SAMHSA PDF Marijuana' class='pdf'></a>
<div class='pdflink'>Tips for Teens - The Truth about Marijuana (PDF 2 pages): <br><a href='https://store.samhsa.gov/system/files/phd641.pdf'>
https://store.samhsa.gov/system/files/phd641.pdf</a>
</div></div>

<p>
<p class='eat'>
<b>How to Talk About Marijuana with a Teen:</b><br>
The parts of the adolescent brain that develop first are those responsible for physical coordination, emotion and motivation. However, the part of the brain that controls reasoning and impulses - known as the prefrontal cortex - does not fully mature until the age of 25. It's as if, while the other parts of the brain are shouting, the prefrontal cortex is not quite ready to play referee. This can have noticeable effects on behavior. Unfortunately, there isn't a script for talking about marijuana, but there are some common arguments and questions that you're likely to hear - and suggestions for how to respond.
</p><p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugfree.php'><img src='/images/drugfreeworld.gif' alt='Foundation for a Drug-Free World' title='Foundation for a Drug-Free World' class='logo'></a>
<div class='talllink'>How to Talk About Marijuana: <br><a href='https://drugfree.org/article/how-to-talk-about-marijuana/'>
https://drugfree.org/article/how-to-talk-about-marijuana/</a>
</div></div>

<p>
<b>Scope of the Youth Issue:</b><br>
Marijuana Use in the United States In 2015: more than 22 million Americans aged 12 or older were current users of marijuana.
<ul><li>Adolescents aged 12-17: 1.8 million
</li><li>Young adults aged 18-25: 6.9 million
</li><li>Adults aged 26 or older: 13.6 million
</li></ul>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/dea.php'><img src='/images/dea.gif' alt='DEA' title='DEA' class='logo'></a>
<a href='https://www.dea.gov/sites/default/files/2018-07/DEA-Marijuana-Prevention-2017-ONLINE.PDF'><img src='/images/marijuana-dea-pdf.png' alt='DEA PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Preventing Marijuana use among youth and young adults (PDF 8 pages): <br><a href='https://www.dea.gov/sites/default/files/2018-07/DEA-Marijuana-Prevention-2017-ONLINE.PDF'>
https://www.dea.gov/sites/default/files/2018-07/DEA-Marijuana-Prevention-2017-ONLINE.PDF</a><br>
</div></div>

<p>
<b>Does Persistent Cannabis Use Show IQ Decline?</b><br>
Persistent cannabis use over 20 y was associated with neuropsychological decline, and greater decline was evident for more persistent users. This effect was concentrated among adolescent-onset cannabis users, a finding consistent with results of several studies showing executive functioning or verbal IQ deficits among adolescent-onset but not adult-onset chronic cannabis users, as well as studies showing impairment of learning, memory, and executive functions in samples of adolescent cannabis users. Increasing efforts should be directed toward delaying the onset of cannabis use by young people, particularly given the recent trend of younger ages of cannabis-use initiation in the United States and evidence that fewer adolescents believe that cannabis use is associated with serious health risk. 
<p>
<p class='update'>
In the present study, the most persistent adolescent-onset cannabis users evidenced an average 8-point IQ decline from childhood to adulthood. 
</p>
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/pnas.php'><img src='/images/pnas.gif' alt='Proceedings of the National Academy of Sciences' title='Proceedings of the National Academy of Sciences' class='logo'></a>
<div class='link'>Study: Persistent cannabis users show neuropsychological decline from childhood to midlife: <br><a href='https://www.pnas.org/content/109/40/E2657'>
https://www.pnas.org/content/109/40/E2657</a>
</div></div> 

<p>
<b>Is Marijuana a Gateway Drug:</b><br>
One common myth is that marijuana is a gateway drug that almost always leads to the use of "harder" drugs. While there is some evidence that exposure to marijuana may make it easier to use other substances, the National Institute on Drug Abuse (NIDA) suggests that most people who use marijuana do not go on to try to become addicted to other drugs.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/verywellmind.php'><img src='/images/verywellmind.gif' alt='verywellmind.com' title='verywellmind.com' class='logo'></a>
<div class='link'>Marijuana: Myths, Effects, Risks, and How to Get Help: <br><a href='https://www.verywellmind.com/basic-facts-about-marijuana-67790'>
https://www.verywellmind.com/basic-facts-about-marijuana-67790</a>
</div></div>

<p>
<b>Is it possible to "overdose" or have a "bad reaction" to marijuana?</b><br>
A fatal overdose is unlikely, but that doesn't mean marijuana is harmless. The signs of using too much marijuana are similar to the typical effects of using marijuana but more severe. These signs may include extreme confusion, anxiety, paranoia, panic, fast heart rate, delusions or hallucinations, increased blood pressure, and severe nausea or vomiting. In some cases, these reactions can lead to unintentional injury such as a motor vehicle crash, fall, or poisoning.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/cdc.php'><img src='/images/cdc.gif' alt='Center for Disease Control and Prevention' title='Center for Disease Control and Prevention' class='logo'></a>
<div class='link'>Is it possible to "overdose" or have a "bad reaction" to marijuana?<br><a href='https://www.cdc.gov/marijuana/faqs/overdose-bad-reaction.html'>
https://www.cdc.gov/marijuana/faqs/overdose-bad-reaction.html</a>
</div></div>

<p>
<b>Pregnancy:</b><br>
Most studies have not found an increase in the chance for birth defects among babies prenatally exposed to "occasional" marijuana use. It is difficult to accurately study marijuana use during pregnancy. Differences in brain activity, behavior, and sleeping patterns of infants and children exposed to marijuana in pregnancy have been reported in some studies. It is believed that these children might have more problems with attention, impulsive behavior, short term memory, academic performance and difficulty at work as an adult. These problems have been seen more often in children whose mothers were "heavy" marijuana users (smoked one or more marijuana cigarettes per day). The evidence is not conclusive and some studies report conflicting results. While most studies are reassuring regarding birth defects, without good studies among heavy marijuana users, and because of other potential pregnancy complications it is best to avoid marijuana during pregnancy.
<p>
<b>Breastfeeding:</b><br>
Marijuana can be passed to infants through their mother's breast milk. Marijuana may also affect the quality and quantity of breast milk that you make. There are no good studies on how marijuana in breast milk might affect a nursing baby. Although no consistent effects have been noticed in infants exposed to marijuana through breast milk, the American Academy of Pediatrics and the Academy of Breastfeeding Medicine advise that breastfeeding mothers avoid using marijuana.
<p>
<b>Fertility:</b><br>
In women, long-term use of marijuana may affect the menstrual cycle and lead to a reduction in hormones involved in reproduction and fertility. In men, an association with reduced sperm count has been seen. These side effects might make it harder to get pregnant. The effects on fertility appear to go away when marijuana use is stopped.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/mothertobaby.php'><img src='/images/mothertobaby.gif' alt='mothertobaby.org' title='mothertobaby.org' class='logo'></a>
<a href='https://mothertobaby.org/fact-sheets/marijuana-pregnancy/pdf/'><img src='/images/marijuana-mothertobaby-pdf.png' alt='Mothertobaby PDF Marijuana' class='pdf'></a>
<div class='pdflink'>Marijuana Fact Sheet (PDF 3 pages): <br><a href='https://mothertobaby.org/fact-sheets/marijuana-pregnancy/pdf/'>
https://mothertobaby.org/fact-sheets/marijuana-pregnancy/pdf/</a><br>
</div></div>

<p>
<b>Can medical marijuana help with seizure disorders?</b><br>
Medical marijuana received a lot of attention a few years ago when parents said that a special form of the drug helped control seizures in their children. The FDA recently approved Epidiolex, which is made from <a href='https://www.nonpsychotoxic.com/cbd-explained.php'>CBD</a>, as a therapy for people with very severe or hard-to-treat seizures. In studies, some people had a dramatic drop in seizures after taking this drug.
<p>
<b>Has the FDA approved medical marijuana?</b><br>
The FDA has approved two man-made cannabinoid medicines - dronabinol (Marinol, Syndros) and nabilone (Cesamet) - to treat nausea and vomiting from chemotherapy. The cannabidiol Epidiolex was approved in 2018 for treating seizures associated with two rare and severe forms of epilepsy, Lennox-Gastaut syndrome and Dravet syndrome.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/webmd.php'><img src='/images/webmd.gif' alt='webmd.com' title='webmd.com' class='logo'></a>
<div class='link'>Medical Marijuana FAQ: <br><a href='https://www.webmd.com/a-to-z-guides/medical-marijuana-faq'>
https://www.webmd.com/a-to-z-guides/medical-marijuana-faq</a>
</div></div>
 
<p>
<b>Medical Marijuana:</b><br>
The most common use for medical marijuana in the United States is for pain control. While marijuana isn't strong enough for severe pain (for example, post-surgical pain or a broken bone), it is quite effective for the chronic pain that plagues millions of Americans, especially as they age. Part of its allure is that it is clearly safer than opiates (it is impossible to overdose on and far less addictive) and it can take the place of NSAIDs such as Advil or Aleve, if people can't take them due to problems with their kidneys or ulcers or GERD. In particular, marijuana appears to ease the pain of multiple sclerosis, and nerve pain in general. This is an area where few other options exist, and those that do, such as Neurontin, Lyrica, or opiates are highly sedating. Patients claim that marijuana allows them to resume their previous activities without feeling completely out of it and disengaged. Along these lines, marijuana is said to be a fantastic muscle relaxant, and people swear by its ability to lessen tremors in Parkinson's disease. I have also heard of its use quite successfully for fibromyalgia, endometriosis, interstitial cystitis, and most other conditions where the final common pathway is chronic pain.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/harvardhealth.php'><img src='/images/harvardhealth.gif' alt='Harvard Medical School' title='Harvard Medical School' class='logo'></a>
<div class='link'>Medical Marijuana: <br><a href='https://www.health.harvard.edu/blog/medical-marijuana-2018011513085'>
https://www.health.harvard.edu/blog/medical-marijuana-2018011513085</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/emcdda.php'><img src='/images/emcdda.gif' alt='European Monitoring Centre for Drugs and Drug Addiction' title='European Monitoring Centre for Drugs and Drug Addiction' class='logo'></a>
<a href='https://www.emcdda.europa.eu/system/files/publications/10171/20185584_TD0618186ENN_PDF.pdf'><img src='/images/marijuana-emcdda-pdf.png' alt='EMCDDA PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Medical use of cannabis and cannabinoids (PDF 48 pages): <br><a href='http://www.emcdda.europa.eu/system/files/publications/10171/20185584_TD0618186ENN_PDF.pdf'>
http://www.emcdda.europa.eu/system/files/publications/10171/20185584_TD0618186ENN_PDF.pdf</a>
</div></div>

<p>
<blockquote class='dgidb'>
<b>Street Names:</b><br>
Aunt Mary, BC Bud, Chronic, Dope, Gangster, Ganja, Grass, Hash, Herb, Joint, Mary Jane, Mota, Pot, Reefer, Sinsemilla, Skunk, Smoke, Weed, Yerba 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/dea.php'><img src='/images/dea.gif' alt='DEA' title='DEA' class='logo'></a>
<a href='https://www.dea.gov/sites/default/files/sites/getsmartaboutdrugs.com/files/publications/DoA_2017Ed_Updated_6.16.17.pdf#page=74'><img src='/images/marijuana-cannabis-dea-pdf.png' alt='DEA PDF Marijuana / Cannabis' class='pdf'></a>
<div class='tallpdflink'>Marijuana/Cannabis (PDF page 74 of 94): <br><a href='https://www.dea.gov/sites/default/files/sites/getsmartaboutdrugs.com/files/publications/DoA_2017Ed_Updated_6.16.17.pdf#page=74'>
https://www.dea.gov/sites/default/files/sites/getsmartaboutdrugs.com/files/publications/DoA_2017Ed_Updated_6.16.17.pdf#page=74</a><br>
</div></div>
</blockquote>

<p>
<b>Effects of Marijuana:</b><br>
The effects of the 120-plus cannabinoids present in cannabis are mostly unknown, but the most potent psychoactive agent identified to date is THC. Some studies have shown that THC affects areas of the brain that control memory creation and attention. It also disrupts other parts of the brain, adversely affecting balance, posture, coordination, and reaction time. People use marijuana to achieve a feeling of elation (a high), giddiness, and relaxation. Marijuana also produces sensory perception changes; colors may seem brighter, music more vivid, and emotions more profound. Some people experience feelings of paranoia, increase in appetite, higher heart rate, reduction in blood pressure, nausea, even though some cannabinoids may help reduce nausea.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/medicalnewstoday.php'><img src='/images/medicalnewstoday.gif' alt='Medical News Today' title='Medical News Today' class='logo'></a>
<div class='talllink'>Everything you need to know about marijuana (cannabis): <br><a href='https://www.medicalnewstoday.com/articles/246392.php'>
https://www.medicalnewstoday.com/articles/246392.php</a>
</div></div>

<p>
<b>THC Extractions:</b><br>
Marijuana concentrates contain extraordinarily high THC levels that could range from 40 to 80 percent. This form of marijuana can be up to four times stronger in THC content than high grade or top shelf marijuana, which normally measures around 20 percent THC levels. Many users of marijuana concentrates prefer the e-cigarette/vaporizer because it's smokeless, odorless, and easy to hide or conceal. The user takes a small amount of marijuana concentrate, referred to as a "dab," then heats the substance using the e-cigarette/vaporizer producing vapors that ensures an instant "high" effect upon the user. Using an e-cigarette/vaporizer to ingest marijuana concentrates is commonly referred to as "dabbing" or "vaping." Common street names include: 710 (the word "OIL" flipped and spelled backwards), wax, ear wax, honey oil, budder, butane hash oil, butane honey oil (BHO), shatter, dabs (dabbing), black glass, and errl.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/getsmartaboutdrugs.php''><img src='/images/getsmartaboutdrugs.gif' alt='DEA' title='DEA' class='logo'></a>
<a href='https://www.getsmartaboutdrugs.gov/sites/getsmartaboutdrugs.com/files/files/Marijuana%20Concentrates_R.pdf'><img src='/images/marijuana-getsmartaboutdrugs-pdf.png' alt='Getsmartaboutdrugs PDF Marijuana' class='pdf'></a>
<div class='pdflink'>Marijuana Concentrates Drug Fact Sheet (PDF 2 pages): <br><a href='https://www.getsmartaboutdrugs.gov/sites/getsmartaboutdrugs.com/files/files/Marijuana%20Concentrates_R.pdf'>
https://www.getsmartaboutdrugs.gov/sites/getsmartaboutdrugs.com/files/files/Marijuana%20Concentrates_R.pdf</a>
</div></div>

<p>
<b>Q: My downstairs neighbor smokes marijuana every night on his balcony. Will I test positive for marijuana from the second-hand smoke?</b><br>
No. It is possible THC (the psychoactive ingredient in marijuana) may be in your system and you could experience a "contact high," but even this is doubtful under these circumstances. With the initial and confirmatory concentration cut-off levels established by the Substance Abuse and Mental Health Services Administration (SAMSHA), passive inhalation will not produce a positive test result for marijuana.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/navy.php'><img src='/images/navy.gif' alt='US NAVY' title='US NAVY' class='logo'></a>
<a href='https://www.secnav.navy.mil/rda/workforce/Documents/Marijuana-Factsheet.pdf'><img src='/images/marijuana-navy-pdf.png' alt='Navy PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Marijuana Fact Sheet: <br><a href='https://www.secnav.navy.mil/rda/workforce/Documents/Marijuana-Factsheet.pdf'>
https://www.secnav.navy.mil/rda/workforce/Documents/Marijuana-Factsheet.pdf</a>
</div></div>

<p>
<b>Does marijuana impair driving the way alcohol does?</b><br>
Yes and no. Marijuana can affect perception and psychomotor performance, changes that could impair driving ability. But in driving studies, marijuana produces little or no car-handling impairment - consistently less than produced by moderate doses of alcohol and many legal medications. Mixing marijuana and alcohol together amplifies potential risks. Surveys of fatally injured drivers show that when THC is detected in the blood, alcohol is often detected as well. That said, it is never a good idea to get behind the wheel when intoxicated, even if just from marijuana alone.For some people, marijuana may play a role in bad driving, but the overall rate of highway accidents does not appear to be significantly affected by marijuana's widespread use. Also, people who frequently use marijuana appear to develop a tolerance to marijuana's impairing effects.  
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/drugpolicy.php'><img src='/images/drugpolicy.gif' alt='Drugpolicy.org' title='Drugpolicy.org' class='logo'></a>
<a href='https://drugpolicy.org/sites/default/files/dpa_marijuana_booklet_january2018_0.pdf'><img src='/images/marijuana-drugpolicy-pdf.png' alt='Drugpolicy PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Marijuana Facts (PDF 28 pages): <br><a href='http://www.drugpolicy.org/sites/default/files/dpa_marijuana_booklet_january2018_0.pdf'>
http://www.drugpolicy.org/sites/default/files/dpa_marijuana_booklet_january2018_0.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/cdc.php'><img src='/images/cdc.gif' alt='Center for Disease Control and Prevention' title='Center for Disease Control and Prevention' class='logo'></a>
<a href='https://www.cdc.gov/marijuana/pdf/marijuana-driving-508.pdf'><img src='/images/marijuana-cdc-pdf.png' alt='CDC PDF Marijuana' class='pdf'></a>
<div class='pdflink'>What You Need to Know About Marijuana Use and Driving (PDF 2 pages): <br><a href='https://www.cdc.gov/marijuana/pdf/marijuana-driving-508.pdf'>
https://www.cdc.gov/marijuana/pdf/marijuana-driving-508.pdf</a>
</div></div>

<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/crs.php'><img src='/images/crs.gif' alt='US Library of Congress Congressinal Research Service' title='US Library of Congress Congressinal Research Service' class='logo'></a>
<a href='https://fas.org/sgp/crs/misc/R45719.pdf'><img src='/images/marijuana-fas-pdf.png' alt='FAS PDF Marijuana' class='pdf'></a>
<div class='tallpdflink'>Marijuana Use and Highway Safety (PDF 14 pages): <br><a href='https://fas.org/sgp/crs/misc/R45719.pdf'>
https://fas.org/sgp/crs/misc/R45719.pdf</a>
</div></div>

<p>
<b>Drug Testing Marijuana:</b><br>
The initial effects created by the THC in marijuana wear off after an hour or two, but the chemicals stay in your body for much longer. The terminal half-life of THC can range from about 20 hours to 10 days, depending on the amount and potency of the marijuana used. This means that if you take 1 milligram of THC that has a half-life of 20 hours, you will still have 0.031 milligrams of THC in your body more than four days later. The longer the half-life, the longer the THC lingers in your body. In 2011, 57 percent of U.S. businesses required prospective employees to pass a drug test. Drug tests detect the five metabolites that THC breaks down into before passing into urine. Detectable amounts can remain in the system for several days or weeks following use, depending on potency and amount consumed. One of the most common tests is the immunoassay, in which urine is mixed with a solution containing an antibody specific to certain metabolites, typically tagged with fluorescent dye or a radioactive substance. The amount of fluorescent light or radioactivity indicates the concentration of metabolites in the sample.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/howstuffworks.php'><img src='/images/howstuffworks.gif' alt='howstuffworks.com' title='howstuffworks.com' class='logo'></a>
<div class='link'>How Marijuana Works: <br><a href='https://science.howstuffworks.com/marijuana5.htm'>
https://science.howstuffworks.com/marijuana5.htm</a>
</div></div>

<p>
<b>Curaleaf the World's Biggest Marijuana Seller:</b><br>
The American marijuana chain Curaleaf Holdings solidified its lead as the country's biggest legal cannabis operation, saying Wednesday it has agreed to buy a privately held rival GR Companies. The chain, based in the Midwest, operates 20 dispensaries under the Grassroots name and has licenses for 41 more. The combined entity will cover 19 states, with 68 operating dispensaries and licenses for an additional 63. Its revenues would have exceeded those of any pot producer - including Canadian leaders like Canopy Growth (CGC) and Aurora Cannabis (ACB) - at more than $250 million in 2018 and nearly $90 million in the March 2019 quarter. The consensus forecast for Curaleaf sales in 2020 is about $900 million, according to FactSet. Grassroots has been reported to be on track for 2020 sales of $350 million. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/barrons.php'><img src='/images/barrons.gif' alt='barrons.com' title='barrons.com' class='logo'></a>
<div class='link'>Merger Makes Curaleaf the World's Biggest Marijuana Seller: <br><a href='https://www.barrons.com/articles/marijuana-merger-curaleaf-cura-partners-biggest-dealer-51556719056'>
https://www.barrons.com/articles/marijuana-merger-curaleaf-cura-partners-biggest-dealer-51556719056</a>
</div></div>

<p>
<b>The Marijuana Market is Significant:</b><br>
The total cannabis market in Canada, including medical and illegal as well as legal recreational products, is expected to generate up to $7.17 billion in total sales in 2019. Legal sales are expected to contribute more than half of this total - up to $4.34 billion - in the first year. Current and likely consumers expect to pay slightly more for legal products, with the former saying they're willing to pay 10 percent more.
<p>
<b>Majority of recreational cannabis sold will be legal:</b><br>
Canadians who are already consuming cannabis expect to buy nearly two-thirds of their products from legal retailers once they can. High product quality and integrity (as affirmed by quality testing) as well as a range of competitive price points will be needed to persuade current consumers to move their purchases over to legal sources. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/deloitte.php'><img src='/images/deloitte.gif' alt='deloitte.com' title='deloitte.com' class='logo'></a>
<a href='https://www2.deloitte.com/content/dam/Deloitte/ca/Documents/consulting/ca-cannabis-2018-report-en.PDF'><img src='/images/marijuana-deloitte-pdf.png' alt='Deloitte PDF Marijuana' class='pdf'></a>
<div class='pdflink'>A society in transition, an industry ready to bloom 2018 cannabis report (PDF 36 pages): <br><a href='https://www2.deloitte.com/content/dam/Deloitte/ca/Documents/consulting/ca-cannabis-2018-report-en.PDF'>
https://www2.deloitte.com/content/dam/Deloitte/ca/Documents/consulting/ca-cannabis-2018-report-en.PDF</a><br>
</div></div>

<p>
<b>Niche branding, as with wines?</b><br>
Now that adult marijuana use is legal in California, the state government is starting to write new rules to treat marijuana growers someone like winemakers and allow areas to be considered an official growing region. The hope is that, by doing so, it could provide a lifeline for small farmers. The state government of California is currently developing rules that will define whether a geographic area can be deemed a marijuana growing region. For small farmers, who are threatened by industrial competitors and the cost of regulation, survival may depend on customers caring about the specific location and soil in which their cannabis is grown.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/pbs.php'><img src='/images/pbs.gif' alt='PBS' title='PBS' class='logo'></a>
<div class='link'>Why small cannabis growers want to produce the Champagne of pot: <br><a href='https://www.pbs.org/newshour/show/can-craft-cannabis-compete-with-big-marijuana'>
https://www.pbs.org/newshour/show/can-craft-cannabis-compete-with-big-marijuana</a>
</div></div>

]]></description>
	<link>https://www.nonpsychotoxic.com/substances/marihuana.php</link>
</item>

<item>
	<title></title>
	<pubDate>Sun, 13 Dec 2020 00:00:00 +0000</pubDate>
	<category>Latest from nonpsychotoxic.com Controled Substances List</category>
	<guid>https://www.nonpsychotoxic.com/substances/hallucinogens.php</guid>
	<description><![CDATA[Hallucinogens are a diverse group of drugs that alter perception, thoughts, and feelings. They cause hallucinations, or sensations and images that seem real though they are not. Some hallucinogens also cause users to feel out of control or disconnected from their body and environment.
<p>
People use hallucinogens in a wide variety of ways, including smoking, snorting, and absorbing through the lining in the mouth.
<p>
Hallucinogens interfere with actions of brain chemicals responsible for functions that include:
<ul> <li>Mood</li>
 <li>Sensory perception</li>
 <li>Sleep</li>
 <li>Body temperature</li>
 <li>Muscle control</li>
 <li>Pain perception</li>
 <li>Memory</li></ul>
<p>
The effects of hallucinogens can begin within 20 to 90 minutes and can last as long as 6 to 12 hours.
<p>
Along with hallucinations, other short-term general effects of hallucinogens include:
<ul>
 <li>Increased heart rate</li>
 <li>Nausea</li>
 <li>Intensified feelings and sensory experiences</li>
 <li>Changes in sense of time</li></ul>
<p>
Persistent psychosis and flashbacks are two long-term effects associated with some hallucinogens.
<p>
Evidence indicates that certain hallucinogens can be addictive or that people can develop a tolerance to them.
<p>
There are no government-approved medications to treat addiction to hallucinogens. Scientists need more research to find out if behavioral therapies are effective for addiction to hallucinogens.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/nida.php'><img src='/images/nida.gif' alt='National Institute on Drug Abuse' title='National Institute on Drug Abuse' class='logo'></a>
<div class='link'>Hallucinogens DrugFacts: <br><a href='https://www.drugabuse.gov/publications/drugfacts/hallucinogens'>
https://www.drugabuse.gov/publications/drugfacts/hallucinogens</a>
</div></div>

<p>
Hallucinogens are found in plants and fungi or are synthetically produced and are among the oldest known group of drugs used for their ability to alter human perception and mood. Hallucinogens can be synthetically produced or are found in plants. Hallucinogens come in a variety of forms. <a href='https://www.nonpsychotoxic.com/substances/mdma.php'>MDMA or ecstasy</a> tablets are sold in many colors with a variety of logos to attract youth. <a href='https://www.nonpsychotoxic.com/substances/lysergic-acid-diethylamide.php'>LSD</a> is sold in the form of impregnated paper (blotter acid), typically imprinted with colorful graphic designs.
<p>
The most commonly abused hallucinogens are <a href='https://www.nonpsychotoxic.com/substances/psilocybin.php'>PSILOCYBIN (magic mushrooms)</a>, LSD, and MDMA (ecstasy). Hallucinogens are typically taken orally or can be smoked. 
<p>
Sensory effects include perceptual distortions that vary with dose, setting, and mood. Psychic effects include distortions of thought associated with time and space. Time may appear to stand still, and forms and colors seem to change and take on new significance. We e k s or even months after some hallucinogens have been taken, the user may experience flashbacks - fragmentary recurrences of certain aspects of the drug experience in the absence of actually taking the drug. The occurrence of a flashback is unpredictable, but is more likely to occur during times of stress and seems to occur more frequently in younger individuals. With time, these episodes diminish and become less intense. 
<p>
Deaths exclusively from acute overdose of LSD, magic mushrooms, and <a href='https://www.nonpsychotoxic.com/substances/mescaline.php'>mescaline</a> are extremely rare. Deaths generally occur due to suicide, accidents, and dangerous behavior, or due to the person inadvertently eating poisonous plant material. 
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/dea.php'><img src='/images/dea.gif' alt='Drug Enforcement Administration' title='Drug Enforcement Administration' class='logo'></a>
<a href='https://www.dea.gov/sites/default/files/2018-06/drug_of_abuse.pdf#%5B%7B%22num%22%3A348%2C%22gen%22%3A0%7D%2C%7B%22name%22%3A%22XYZ%22%7D%2C0%2C792%2Cnull%5D'><img src='/images/hallucinogens-dea-pdf.png' alt='DEA PDF Hallucinogens' class='pdf'></a>
<div class='tallpdflink'>DEA resource guide (PDF page 64 of 94): <br><a href='https://www.dea.gov/sites/default/files/2018-06/drug_of_abuse.pdf#%5B%7B%22num%22%3A348%2C%22gen%22%3A0%7D%2C%7B%22name%22%3A%22XYZ%22%7D%2C0%2C792%2Cnull%5D'>
https://www.dea.gov/sites/default/files/2018-06/drug_of_abuse.pdf#%5B%7B%22num%22%3A348%2C%22gen%22%3A0%7D%2C%7B%22name%22%3A%22XYZ%22%7D%2C0%2C792%2Cnull%5D</a><br>
</div></div>


<p>
<blockquote class='wide' style='background:-color: #ffe4d4; font-size: calc(11px + 0.50vw); line-height: calc(11px + 1.0vw); border-radius: 6px; border: 0;'>
Hallucinogens are a class of  drugs that cause hallucinations - profound distortions in a person's perceptions of  reality. Hallucinogens can be found in some plants and mushrooms (or their extracts) or can be man-made, and they are commonly divided into two broad categories: classic hallucinogens (such as <a href='https://www.nonpsychotoxic.com/substances/lysergic-acid-diethylamide.php'>LSD</a>) and dissociative drugs (such as <a href='https://www.nonpsychotoxic.com/substances/phencyclidine.php'>PCP</a>). When under the influence of  either type of  drug, people often report experiencing rapid, intense emotional swings and seeing images, hearing sounds, and feeling sensations that seem real but are not.  While the exact mechanisms by which hallucinogens and dissociative drugs cause their effects are not yet clearly understood, research suggests that they work at least partially by temporarily disrupting communication between neurotransmitter systems throughout the brain and spinal cord.
<p>
<div style='margin:0px -15px 0px -15px;'>
<table style='margin-left: auto; margin-right: auto; background-color: #ffffff; box-shadow: 0 24px 16px -20px rgba(0,0,0,.15);'>
<thead><tr><th colspan='2' style='background-color: #174e9a; color: #ffffff; padding: 10px; font-size: calc(11px + 0.50vw);'>General Common Effects of Dissociative Drugs</th></tr></thead>
<tbody>
<tr><td style='background-color: #dbedfa; color: #174e9a; width: 50%; padding: 6px; font-size: calc(11px + 0.50vw); font-weight: bold;'>Low to Moderate Doses</td>
<td style='background-color: #fedbc6; color: #fc4c00; width: 50%; padding: 6px; font-size: calc(11px + 0.50vw); font-weight: bold;'>High Doses</td>
</tr>
<tr><td style='background-color: #dbedfa; color: #174e9a; width: 50%; vertical-align: top; padding: 6px;'><ul class='small'><li>Numbness</li><li>Hallucinations</li><li>Loss of coordination, disorientation, and confusion</li><li>Dizziness, nausea, vomiting</li><li>Changes in sensory perceptions (such as sight, sound, shapes, time, and body image)</li><li>Hallucinations</li><li>Feelings of detachment from self and environment</li><li>Increase in blood pressure, heart rate, respiration, and body temperature</li></ul></td>
<td style='background-color: #fedbc6; color: #fc4c00; width: 50%; vertical-align: top; padding: 6px;'><ul class='small'><li>Hallucinations</li><li>Memory loss</li><li>Physical distress, including dangerous changes in blood pressure, heart rate, respiration, and body temperature</li><li>Marked psychological distress, including feelings of extreme panic, fear, anxiety, paranoia, invulnerability, exaggerated strength, and aggression</li><li>Use with high doses of alcohol or other central nervous system depressants can lead to respiratory distress or arrest, resulting in death</li></ul>
</td></tr></tbody></table>
</div>
<p>
<b>Long-Term Effects of Hallucinogens:</b><p>
<b>Persistent Psychosis:</b><br>
<ul><li>Visual disturbances</li><li>Disorganized thinking</li><li>Paranoia</li><li>Mood disturbances</li></ul>
<p>
<b>Hallucinogen Persisting Perception Disorder (HPPD):</b><br>
<ul><li>Hallucinations</li><li>Other visual disturbances (such as seeing halos or trails attached to moving objects)</li><li>Symptoms sometimes mistaken for neurological disorders (such as stroke or brain tumor)</li></ul>
<p>

<b style='color: #ff5000; font-size: 16px; font-weight: bold;'>Hallucinogens Glossary:</b><p>
<b>Central Nervous System:</b> The brain and spinal cord.
<p>
<b>Cerebral cortex:</b> The region of the brain responsible for cognitive functions including reasoning, mood, and perception of stimuli. 
<p>
<b>Dissociative:</b> a type of compound, such as phencyclidine or ketamine, that produces an anesthetic effect characterized by a feeling of being detached from the physical self.
<p>
<b>DXM:</b> A common street name for dextromethorphan. 
<p>
<b>Flashback:</b> A sudden but temporary recurrence of aspects of a drug experience (including sights, sounds, and feelings) that may occur days, weeks, or even more than a year after hallucinogenic drug use. 
<p>
<b>Glutamate:</b> An excitatory neurotransmitter found throughout the brain that influences the reward system and is involved in learning and memory, among other functions.
<p>
<b>Hallucinogen:</b> A drug that produces hallucinations - distortions in perception of sights and sounds - and disturbances in emotion, judgment, and memory. 
<p>
<b>HPPD:</b> Hallucinogen persisting perception disorder; the spontaneous and sometimes continuous recurrence of perceptual effects of LSD long after an individual has ingested the drug. 
<p>
<b>Kappa opioid receptor:</b> A receptor on nerve cells that is activated by certain opioid-like compounds produced in the body. These receptors differ from those activated by the more commonly known opioids, such as heroin and morphine.
<p>
<b>Neurotransmitter:</b> A chemical compound that acts as a messenger to carry signals from one nerve cell to another. 
<p>
<b>NMDA receptors:</b> N-methyl-D-aspartate receptors, a type of glutamate receptor that is important for learning and memory; it is the target of drugs such as PCP and ketamine. 
<p>
<b>Persistent Psychosis:</b> Unpredictable and long-lasting visual disturbances, dramatic mood swings, and hallucinations experienced by some LSD users after they have discontinued use of the drug. 
<p>
<b>Serotonin:</b> A neurotransmitter involved in a broad range of effects on perception, movement, and emotions. Serotonin and its receptors are the targets of most hallucinogens.
<p>
<div class='source'><a href='https://www.nonpsychotoxic.com/sources/nida.php'><img src='/images/nida.gif' alt='National Institute on Drug Abuse' title='National Institute on Drug Abuse' class='logo'></a>
<a href='https://www.drugabuse.gov/sites/default/files/hallucinogensrrs.pdf'><img src='/images/hallucinogens-drugabuse-pdf.png' alt='Drugabuse PDF Hallucinogens' class='pdf'></a>
<div class='pdflink'>Hallucinogens and Dissociative Drugs Research Report (PDF 8 pages): <br><a href='https://www.drugabuse.gov/sites/default/files/hallucinogensrrs.pdf'>
https://www.drugabuse.gov/sites/default/files/hallucinogensrrs.pdf</a>
</div></div>
</blockquote>

<p>
<div class="youtube"> <iframe class="youtubeiframe" 
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<div class='link'>why why why why why why why Blog - Experience Reports on practically every hallucinogenic substance within the psychedelic-dissociative-deliriant trifecta: <br><a href='http://nervewing.blogspot.com/'>
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<table cellspacing="0" cellpadding="0" border="0"><tbody><tr><td><b>Hallucinogens:</b><br></td></tr><tr><td valign='top'>
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