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United States News
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Title: The Great Marijuana Debate -- Your Life May Depend on it
Source: Blacklisted News
URL Source: http://www.blacklistednews.com/The_ ... d_on_it/59195/0/38/38/Y/M.html
Published: Jun 17, 2017
Author: Patrick J McShay
Post Date: 2017-06-18 12:51:27 by Deckard
Keywords: None
Views: 2069
Comments: 15

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"Good people don't smoke Marijuana" - *Attorney General Jeff Sessions

"Mr Sessions stands against an overwhelming majority of Americans and even, sadly, against veterans and other people who we now know conclusively are helped dramatically by Medical Marijuana". - *Congressman Dana Rohrabacher

"Medical Marijuana in it's natural form is one of the safest, therapeutically active substances known to man."- *DEA Judge Francis Young- 1988

If I didn't know better, after reading Attorney General Jeff Sessions uneducated and incredibly ignorant views on the issue of Marijuana legalization, whether medical or recreational, I would have thought that he'd had a close friend or family member who had died of a Marijuana overdose. But I do know better, and so do most Americans. Does Jeff Sessions know better? Sadly, I'm not sure he does.

Mr Sessions has always claimed to be a strong supporter of states rights, as has Trump. Trump said on the campaign trail that Marijuana was a states rights issue, and that as President it would remain so. Earlier this year Sessions told members of Congress that he would not be going after States with legal Cannabis. That has apparently changed.

Sessions recently sent a letter to Congress, In which he urged members not to renew the 2014 Rohrabacher-Farr Amendment, which prevents the Department of Justice from spending federal funds to interfere with state laws on the use, distribution, possession or cultivation of Cannabis.

Despite Sessions claim as a warrior for states rights and the will of the people, he is linking Medical Cannabis to the Opioid crisis, and says Americans need to just say no, or else. Sessions says, "the department must be in a position to combat transnational drug organizations and dangerous drug traffickers who threaten American lives."

I'm not sure Mr Sessions understands how states with legal medical or recreational Cannabis operate. Sessions claims he needs prosecutorial powers, because Marijuana is a horrible drug, fueling a " historic drug epidemic," and apparently he wants to save us from ourselves.

Eight States have legalized recreational use of Marijuana, and 29 States have some form of Medical Marijuana laws on the books. Mr Sessions, who has been a shill for big Tobacco, has argued that "Marijuana is only slightly worse than Heroin."

After Sessions run for the Senate in 1996, it was found that RJ Reynolds Tobacco Company had sent the campaign so much money that they they had exceeded the legal limit, and had had to send some back. Sessions has also received tens of thousands of dollars from the alcohol industry over the years. The National Academy of Sciences and Medicine has rejected the notion that Marijuana is a gateway to other illicit drugs, so why does Sessions keep saying it.

All of his rhetoric sounds like some post "Reefer Madness", cold war era political stooge, owned by big alcohol, big Pharma and the private prison industry. Instead the evidence shows that people are substituting Marijuana for Opioids to manage their pain, with much lower rates of overdoses in states that allow Medical Marijuana. Veterans are turning to Cannabis to treat their PTSD, and just saying no to government approved pharmaceuticals. Another Sessions talking point is crime associated with Pot. A year after legalization, crime in Colorado was down across the board.

Mr Sessions crusade against legal Cannabis isn't just disingenuous, it is cruel and irresponsible. Sessions said recently that he is surprised that more Americans aren't embracing his stance on weed. He should know that a recent Quinnipiac poll showed 94% of respondents approve of doctor prescribed Pot. That is the highest number yet in a poll of this kind.

In Jeff Sessions home state of Alabama, an April, 2017 poll showed 86% of respondents are in favor of legalizing Marijuana for recreational use. 92% said they believe alcohol to be worse than Pot. As of 2016, Alabama law didn't allow initiatives or referendums. The Alabama Legislature recently voted down "Carly's Bill", that would have legalized the use of CBD Oil, that contains little or no THC. How, in this age of the internet can politicians be so out of touch?

Mr Sessions doesn't believe that Marijuana has any medicinal value at all, but US Patent # 6630507 was recently granted to the Department of Health and Human Services. Attorney Sam Mendez, an intellectual property and public policy Lawyer, says it shows a certain amount of hypocrisy from a government that still maintains Cannabis has no medicinal value. If Trump wants to assure victory in 4 years he should legalize Marijuana and send Sessions back to 1950 where he belongs

Lee Carroll Brooker is a 77 year old Alabama resident, and a disabled veteran. Bowman was growing weed on land owned by his son, to deal with chronic pain, and to get off of his doctor prescribed, and Jeff Sessions approved drugs . Bowman was arrested in 2014 and sentenced to a mandatory life sentence for growing weed. His son was also arrested, and received a sentence of 5 years probation. Because Bowman had prior convictions in the state decades ago, he qualified for the mandatory life sentence, even though there was no evidence he was selling the weed. In April, 2016, the Supreme Court refused to hear Bowman's appeal of this harsh sentence.

This must please Sessions and his pals in the private prison industry. Some of Trump and Session's biggest supporters for the Presidency were for profit prison operators. One of the few things Obama got right was ordering the Justice Department to begin phasing out private prison contracts. Recently, private prison industry giant GEO, and another private prison operator Core Civic, each gave $250K to the Trump campaign.

In Sessions financial filing dated December 23, 2016, he disclosed numerous accounts with Vanguard Investments, which owns more private prison stock than any other investment management company.

Marijuana has always been characterized as dangerous, unhealthy and destructive, despite a long history of medicinal efficacy. During the reign of Chinese Emperor Shen Nung, 5000 years ago, Marijuana was used as medicine. A 3700 year old Egyptian papyrus contained medical references to Marijuana and it's healing properties. Around 1450 BC holy anointing oil was described in the original Hebrew version of Exodus. It detailed how Cannabis oil was mixed into jars of Olive oil along with fragrant herbs and used as anointing oil. Cannabis oil was found on the mummy of King Ramses II, who died in 1213 BC.

In ancient Egypt and India Cannabis was used to treat ailments like Rheumatism, Gout, Glaucoma, Nausea, Dysentery, joint pain and labor pains among others. Siddhartha Gautama, the founder of Buddhism, was said to have lived for 6 years on Hemp seeds alone. When Napoleon's Army left Egypt they took Cannabis with them back to Europe, and over a hundred years ago you could buy Cannabis Oil from the Sears Catalog.

An early seventies Harvard Study showed that Cannabis killed Cancer Cells, but because of the ongoing demonization of Pot, further study was always discouraged. Harvard Professor, Lester Grinspoon has studied Cannabis and it's effects for 50 years, and was good friends with astrophysicist and avid Pot smoker, Carl Sagan. Grinspoon attests that Cannabis is non toxic, non addictive and does not cause psychosis or schizophrenia, as some have claimed. This is the dangerous drug Mr Sessions and his ilk are trying to save us from?

Kelly Hauf was diagnosed in 1990 with 2 tumors, one smaller, and a larger one on the frontal lobe of her brain. Surgery was successfully performed and neither Chemotherapy nor radiation were recommended. It was decided that they would monitor her with an MRI every 3 months. The tumor did return, and her surgeon recommended 4 to 6 months of Chemotherapy. The Chemo didn't work, and another surgery would have to be scheduled. she was prescribed anti seizure medication, but because of problems with the medication, she looked for an alternative.

She found that people were having success with Cannabis Oil for seizures, as well as Cancer treatment. Because she lives in a state where Cannabis is illegal, she and her husband planned to stay with their adult daughter in California for the 90 days of Cannabis Oil treatment. After the 90 days of treatment, she went back for her next MRI. While the larger tumor was still there, it looked smaller, and the smaller tumor was gone.

Encouraged, she continued her treatment, increasing her tolerance and her dosage. After 8 months of treatment, her doctors were amazed. Her MRI was reviewed by her Oncologist, a leading Radiologist and a renowned Brain Surgeon, and it was discovered the tumor was completely gone. Today Kelly is Cancer free, and while diet and exercise were part of her treatment, Kelly credits Cannabis Oil with her recovery.

Doug Bench is a retired former judge from Florida. During his time as a judge, Bench sentenced 311 Marijuana offenders to jail. When he was diagnosed with Stage 4 COPD, he knew his options were limited. Modern medicine offers no hope for those with COPD. His doctor gave him 2 to 3 years to live, and told him his condition would continue to worsen.

When Doug's wife suggested Cannabis Oil, he rejected the idea at first, but came around when she threatened to leave him. He had a home in Colorado, and was able to obtain the oil with no problem. He was amazed at how quickly the oil began working. His COPD is in remission, and he has become an advocate for Medical Marijuana legalization.

One of the pioneers of Medical Marijuana in the state of Oregon, Dr Phil Leveque, has prescribed Cannabis for over 5000 patients. He stated, "Marijuana is one of the best bronchodilators, much better than any other class of drug. For respiratory diseases like Asthma and COPD Marijuana can be life saving." Dr Leveque also nixed the notion that smoking Marijuana was bad for the lungs, claiming Cannabinoids are beneficial to Lung Tissue, and smoking Pot can actually improve Lung function.

There are thousands of these stories out there. Cannabis Oil is helping people with a number of serious and life threatening maladies. Recent studies have shown that Cannabis Oil may slow the progression of Alzheimer's, and the oil is being used to treat Autistic children with incredible success. Michael J Fox posted a testimonial on youtube about how Cannabis Oil has helped alleviate his symptoms from Parkinson's Disease. Cannabis Oil must be made available to everyone who needs it.

New VA Secretary David Shulkin in an interview this week said, he believes Marijuana could help veterans with PTSD. Unfortunately he must follow federal law, and Sessions is making progress in this area impossible. Trump vowed to help veterans, and instead he is doing grave damage. 22 vets a month kill themselves and many others are being arrested for treating their PTSD with Cannabis in states where it is still illegal. Look up the Rick Simpson Protocol on youtube and learn how to safely make the oil at home.

We have to make it accessible to people in every state. Cannabis is a God given wonder drug that is being suppressed by imbecilic politico's in Washington. Cancer rates are on the rise and our options for survival should not be limited by ignorant politicians and fussy fundamentalists like Attorney General, Jeff Sessions (1 image)

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Begin Trace Mode for Comment # 5.

#5. To: Deckard (#0)

Allen's Axiom: When all else fails, read the instructions.

For "Authority and criteria for classification of substances," here is the statute.

http://law.justia.com/codes/us/2015/title-21/chapter-13/subchapter-i/part-b/sec.-811/

2015 US Code Title 21 - Food and Drugs (Sections 1 - 2252) Chapter 13 - Drug Abuse Prevention and Control (Sections 801 - 971) Subchapter I - Control and Enforcement (Sections 801 - 904) Part B - Authority to Control; Standards and Schedules (Sections 811 - 814) Sec. 811 - Authority and criteria for classification of substances

21 U.S.C. § 811 (2015)

§811. Authority and criteria for classification of substances

(a) Rules and regulations of Attorney General; hearing

The Attorney General shall apply the provisions of this subchapter to the controlled substances listed in the schedules established by section 812 of this title and to any other drug or other substance added to such schedules under this subchapter. Except as provided in subsections (d) and (e) of this section, the Attorney General may by rule—

(1) add to such a schedule or transfer between such schedules any drug or other substance if he—

(A) finds that such drug or other substance has a potential for abuse, and

(B) makes with respect to such drug or other substance the findings prescribed by subsection (b) of section 812 of this title for the schedule in which such drug is to be placed; or

(2) remove any drug or other substance from the schedules if he finds that the drug or other substance does not meet the requirements for inclusion in any schedule.

Rules of the Attorney General under this subsection shall be made on the record after opportunity for a hearing pursuant to the rulemaking procedures prescribed by subchapter II of chapter 5 of title 5. Proceedings for the issuance, amendment, or repeal of such rules may be initiated by the Attorney General (1) on his own motion, (2) at the request of the Secretary, or (3) on the petition of any interested party.

(b) Evaluation of drugs and other substances

The Attorney General shall, before initiating proceedings under subsection (a) of this section to control a drug or other substance or to remove a drug or other substance entirely from the schedules, and after gathering the necessary data, request from the Secretary a scientific and medical evaluation, and his recommendations, as to whether such drug or other substance should be so controlled or removed as a controlled substance. In making such evaluation and recommendations, the Secretary shall consider the factors listed in paragraphs (2), (3), (6), (7), and (8) of subsection (c) of this section and any scientific or medical considerations involved in paragraphs (1), (4), and (5) of such subsection. The recommendations of the Secretary shall include recommendations with respect to the appropriate schedule, if any, under which such drug or other substance should be listed. The evaluation and the recommendations of the Secretary shall be made in writing and submitted to the Attorney General within a reasonable time. The recommendations of the Secretary to the Attorney General shall be binding on the Attorney General as to such scientific and medical matters, and if the Secretary recommends that a drug or other substance not be controlled, the Attorney General shall not control the drug or other substance. If the Attorney General determines that these facts and all other relevant data constitute substantial evidence of potential for abuse such as to warrant control or substantial evidence that the drug or other substance should be removed entirely from the schedules, he shall initiate proceedings for control or removal, as the case may be, under subsection (a) of this section.

(c) Factors determinative of control or removal from schedules

In making any finding under subsection (a) of this section or under subsection (b) of section 812 of this title, the Attorney General shall consider the following factors with respect to each drug or other substance proposed to be controlled or removed from the schedules:

(1) Its actual or relative potential for abuse.

(2) Scientific evidence of its pharmacological effect, if known.

(3) The state of current scientific knowledge regarding the drug or other substance.

(4) Its history and current pattern of abuse.

(5) The scope, duration, and significance of abuse.

(6) What, if any, risk there is to the public health.

(7) Its psychic or physiological dependence liability.

(8) Whether the substance is an immediate precursor of a substance already controlled under this subchapter.

(d) International treaties, conventions, and protocols requiring control; procedures respecting changes in drug schedules of Convention on Psychotropic Substances

(1) If control is required by United States obligations under international treaties, conventions, or protocols in effect on October 27, 1970, the Attorney General shall issue an order controlling such drug under the schedule he deems most appropriate to carry out such obligations, without regard to the findings required by subsection (a) of this section or section 812(b) of this title and without regard to the procedures prescribed by subsections (a) and (b) of this section.

(2)(A) Whenever the Secretary of State receives notification from the Secretary-General of the United Nations that information has been transmitted by or to the World Health Organization, pursuant to article 2 of the Convention on Psychotropic Substances, which may justify adding a drug or other substance to one of the schedules of the Convention, transferring a drug or substance from one schedule to another, or deleting it from the schedules, the Secretary of State shall immediately transmit the notice to the Secretary of Health and Human Services who shall publish it in the Federal Register and provide opportunity to interested persons to submit to him comments respecting the scientific and medical evaluations which he is to prepare respecting such drug or substance. The Secretary of Health and Human Services shall prepare for transmission through the Secretary of State to the World Health Organization such medical and scientific evaluations as may be appropriate regarding the possible action that could be proposed by the World Health Organization respecting the drug or substance with respect to which a notice was transmitted under this subparagraph.

(B) Whenever the Secretary of State receives information that the Commission on Narcotic Drugs of the United Nations proposes to decide whether to add a drug or other substance to one of the schedules of the Convention, transfer a drug or substance from one schedule to another, or delete it from the schedules, the Secretary of State shall transmit timely notice to the Secretary of Health and Human Services of such information who shall publish a summary of such information in the Federal Register and provide opportunity to interested persons to submit to him comments respecting the recommendation which he is to furnish, pursuant to this subparagraph, respecting such proposal. The Secretary of Health and Human Services shall evaluate the proposal and furnish a recommendation to the Secretary of State which shall be binding on the representative of the United States in discussions and negotiations relating to the proposal.

(3) When the United States receives notification of a scheduling decision pursuant to article 2 of the Convention on Psychotropic Substances that a drug or other substance has been added or transferred to a schedule specified in the notification or receives notification (referred to in this subsection as a "schedule notice") that existing legal controls applicable under this subchapter to a drug or substance and the controls required by the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 301 et seq.] do not meet the requirements of the schedule of the Convention in which such drug or substance has been placed, the Secretary of Health and Human Services after consultation with the Attorney General, shall first determine whether existing legal controls under this subchapter applicable to the drug or substance and the controls required by the Federal Food, Drug, and Cosmetic Act, meet the requirements of the schedule specified in the notification or schedule notice and shall take the following action:

(A) If such requirements are met by such existing controls but the Secretary of Health and Human Services nonetheless believes that more stringent controls should be applied to the drug or substance, the Secretary shall recommend to the Attorney General that he initiate proceedings for scheduling the drug or substance, pursuant to subsections (a) and (b) of this section, to apply to such controls.

(B) If such requirements are not met by such existing controls and the Secretary of Health and Human Services concurs in the scheduling decision or schedule notice transmitted by the notification, the Secretary shall recommend to the Attorney General that he initiate proceedings for scheduling the drug or substance under the appropriate schedule pursuant to subsections (a) and (b) of this section.

(C) If such requirements are not met by such existing controls and the Secretary of Health and Human Services does not concur in the scheduling decision or schedule notice transmitted by the notification, the Secretary shall—

(i) if he deems that additional controls are necessary to protect the public health and safety, recommend to the Attorney General that he initiate proceedings for scheduling the drug or substance pursuant to subsections (a) and (b) of this section, to apply such additional controls;

(ii) request the Secretary of State to transmit a notice of qualified acceptance, within the period specified in the Convention, pursuant to paragraph 7 of article 2 of the Convention, to the Secretary-General of the United Nations;

(iii) request the Secretary of State to transmit a notice of qualified acceptance as prescribed in clause (ii) and request the Secretary of State to ask for a review by the Economic and Social Council of the United Nations, in accordance with paragraph 8 of article 2 of the Convention, of the scheduling decision; or

(iv) in the case of a schedule notice, request the Secretary of State to take appropriate action under the Convention to initiate proceedings to remove the drug or substance from the schedules under the Convention or to transfer the drug or substance to a schedule under the Convention different from the one specified in the schedule notice.

(4)(A) If the Attorney General determines, after consultation with the Secretary of Health and Human Services, that proceedings initiated under recommendations made under paragraph 1 (B) or (C)(i) of paragraph (3) will not be completed within the time period required by paragraph 7 of article 2 of the Convention, the Attorney General, after consultation with the Secretary and after providing interested persons opportunity to submit comments respecting the requirements of the temporary order to be issued under this sentence, shall issue a temporary order controlling the drug or substance under schedule IV or V, whichever is most appropriate to carry out the minimum United States obligations under paragraph 7 of article 2 of the Convention. As a part of such order, the Attorney General shall, after consultation with the Secretary, except such drug or substance from the application of any provision of part C of this subchapter which he finds is not required to carry out the United States obligations under paragraph 7 of article 2 of the Convention. In the case of proceedings initiated under subparagraph (B) of paragraph (3), the Attorney General, concurrently with the issuance of such order, shall request the Secretary of State to transmit a notice of qualified acceptance to the Secretary-General of the United Nations pursuant to paragraph 7 of article 2 of the Convention. A temporary order issued under this subparagraph controlling a drug or other substance subject to proceedings initiated under subsections (a) and (b) of this section shall expire upon the effective date of the application to the drug or substance of the controls resulting from such proceedings.

(B) After a notice of qualified acceptance of a scheduling decision with respect to a drug or other substance is transmitted to the Secretary-General of the United Nations in accordance with clause (ii) or (iii) of paragraph (3)(C) or after a request has been made under clause (iv) of such paragraph with respect to a drug or substance described in a schedule notice, the Attorney General, after consultation with the Secretary of Health and Human Services and after providing interested persons opportunity to submit comments respecting the requirements of the order to be issued under this sentence, shall issue an order controlling the drug or substance under schedule IV or V, whichever is most appropriate to carry out the minimum United States obligations under paragraph 7 of article 2 of the Convention in the case of a drug or substance for which a notice of qualified acceptance was transmitted or whichever the Attorney General determines is appropriate in the case of a drug or substance described in a schedule notice. As a part of such order, the Attorney General shall, after consultation with the Secretary, except such drug or substance from the application of any provision of part C of this subchapter which he finds is not required to carry out the United States obligations under paragraph 7 of article 2 of the Convention. If, as a result of a review under paragraph 8 of article 2 of the Convention of the scheduling decision with respect to which a notice of qualified acceptance was transmitted in accordance with clause (ii) or (iii) of paragraph (3)(C)—

(i) the decision is reversed, and

(ii) the drug or substance subject to such decision is not required to be controlled under schedule IV or V to carry out the minimum United States obligations under paragraph 7 of article 2 of the Convention,

the order issued under this subparagraph with respect to such drug or substance shall expire upon receipt by the United States of the review decision. If, as a result of action taken pursuant to action initiated under a request transmitted under clause (iv) of paragraph (3)(C), the drug or substance with respect to which such action was taken is not required to be controlled under schedule IV or V, the order issued under this paragraph with respect to such drug or substance shall expire upon receipt by the United States of a notice of the action taken with respect to such drug or substance under the Convention.

(C) An order issued under subparagraph (A) or (B) may be issued without regard to the findings required by subsection (a) of this section or by section 812(b) of this title and without regard to the procedures prescribed by subsection (a) or (b) of this section.

(5) Nothing in the amendments made by the Psychotropic Substances Act of 1978 or the regulations or orders promulgated thereunder shall be construed to preclude requests by the Secretary of Health and Human Services or the Attorney General through the Secretary of State, pursuant to article 2 or other applicable provisions of the Convention, for review of scheduling decisions under such Convention, based on new or additional information.

(e) Immediate precursors

The Attorney General may, without regard to the findings required by subsection (a) of this section or section 812(b) of this title and without regard to the procedures prescribed by subsections (a) and (b) of this section, place an immediate precursor in the same schedule in which the controlled substance of which it is an immediate precursor is placed or in any other schedule with a higher numerical designation. If the Attorney General designates a substance as an immediate precursor and places it in a schedule, other substances shall not be placed in a schedule solely because they are its precursors.

(f) Abuse potential

If, at the time a new-drug application is submitted to the Secretary for any drug having a stimulant, depressant, or hallucinogenic effect on the central nervous system, it appears that such drug has an abuse potential, such information shall be forwarded by the Secretary to the Attorney General.

(g) Exclusion of non-narcotic substances sold over the counter without a prescription; dextromethorphan; exemption of substances lacking abuse potential

(1) The Attorney General shall by regulation exclude any non-narcotic drug which contains a controlled substance from the application of this subchapter and subchapter II of this chapter if such drug may, under the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 301 et seq.], be lawfully sold over the counter without a prescription.

(2) Dextromethorphan shall not be deemed to be included in any schedule by reason of enactment of this subchapter unless controlled after October 27, 1970 pursuant to the foregoing provisions of this section.

(3) The Attorney General may, by regulation, exempt any compound, mixture, or preparation containing a controlled substance from the application of all or any part of this subchapter if he finds such compound, mixture, or preparation meets the requirements of one of the following categories:

(A) A mixture, or preparation containing a nonnarcotic controlled substance, which mixture or preparation is approved for prescription use, and which contains one or more other active ingredients which are not listed in any schedule and which are included therein in such combinations, quantity, proportion, or concentration as to vitiate the potential for abuse.

(B) A compound, mixture, or preparation which contains any controlled substance, which is not for administration to a human being or animal, and which is packaged in such form or concentration, or with adulterants or denaturants, so that as packaged it does not present any significant potential for abuse.

(C) Upon the recommendation of the Secretary of Health and Human Services, a compound, mixture, or preparation which contains any anabolic steroid, which is intended for administration to a human being or an animal, and which, because of its concentration, preparation, formulation or delivery system, does not present any significant potential for abuse.

(h) Temporary scheduling to avoid imminent hazards to public safety

(1) If the Attorney General finds that the scheduling of a substance in schedule I on a temporary basis is necessary to avoid an imminent hazard to the public safety, he may, by order and without regard to the requirements of subsection (b) of this section relating to the Secretary of Health and Human Services, schedule such substance in schedule I if the substance is not listed in any other schedule in section 812 of this title or if no exemption or approval is in effect for the substance under section 505 of the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 355]. Such an order may not be issued before the expiration of thirty days from—

(A) the date of the publication by the Attorney General of a notice in the Federal Register of the intention to issue such order and the grounds upon which such order is to be issued, and

(B) the date the Attorney General has transmitted the notice required by paragraph (4).

(2) The scheduling of a substance under this subsection shall expire at the end of 2 years from the date of the issuance of the order scheduling such substance, except that the Attorney General may, during the pendency of proceedings under subsection (a)(1) of this section with respect to the substance, extend the temporary scheduling for up to 1 year.

(3) When issuing an order under paragraph (1), the Attorney General shall be required to consider, with respect to the finding of an imminent hazard to the public safety, only those factors set forth in paragraphs (4), (5), and (6) of subsection (c) of this section, including actual abuse, diversion from legitimate channels, and clandestine importation, manufacture, or distribution.

(4) The Attorney General shall transmit notice of an order proposed to be issued under paragraph (1) to the Secretary of Health and Human Services. In issuing an order under paragraph (1), the Attorney General shall take into consideration any comments submitted by the Secretary in response to a notice transmitted pursuant to this paragraph.

(5) An order issued under paragraph (1) with respect to a substance shall be vacated upon the conclusion of a subsequent rulemaking proceeding initiated under subsection (a) of this section with respect to such substance.

(6) An order issued under paragraph (1) is not subject to judicial review.

(i) Temporary and permanent scheduling of recently emerged anabolic steroids

(1) The Attorney General may issue a temporary order adding a drug or other substance to the definition of anabolic steroids if the Attorney General finds that—

(A) the drug or other substance satisfies the criteria for being considered an anabolic steroid under section 802(41) of this title but is not listed in that section or by regulation of the Attorney General as being an anabolic steroid; and

(B) adding such drug or other substance to the definition of anabolic steroids will assist in preventing abuse or misuse of the drug or other substance.

(2) An order issued under paragraph (1) shall not take effect until 30 days after the date of the publication by the Attorney General of a notice in the Federal Register of the intention to issue such order and the grounds upon which such order is to be issued. The order shall expire not later than 24 months after the date it becomes effective, except that the Attorney General may, during the pendency of proceedings under paragraph (6), extend the temporary scheduling order for up to 6 months.

(3) The Attorney General shall transmit notice of an order proposed to be issued under paragraph (1) to the Secretary of Health and Human Services. In issuing an order under paragraph (1), the Attorney General shall take into consideration any comments submitted by the Secretary in response to a notice transmitted pursuant to this paragraph.

(4) A temporary scheduling order issued under paragraph (1) shall be vacated upon the issuance of a permanent scheduling order under paragraph (6).

(5) An order issued under paragraph (1) is not subject to judicial review.

(6) The Attorney General may, by rule, issue a permanent order adding a drug or other substance to the definition of anabolic steroids if such drug or other substance satisfies the criteria for being considered an anabolic steroid under section 802(41) of this title. Such rulemaking may be commenced simultaneously with the issuance of the temporary order issued under paragraph (1).

(j) Interim final rule; date of issuance; procedure for final rule

(1) With respect to a drug referred to in subsection (f), if the Secretary of Health and Human Services recommends that the Attorney General control the drug in schedule II, III, IV, or V pursuant to subsections (a) and (b), the Attorney General shall, not later than 90 days after the date described in paragraph (2), issue an interim final rule controlling the drug in accordance with such subsections and section 812(b) of this title using the procedures described in paragraph (3).

(2) The date described in this paragraph shall be the later of—

(A) the date on which the Attorney General receives the scientific and medical evaluation and the scheduling recommendation from the Secretary of Health and Human Services in accordance with subsection (b); or

(B) the date on which the Attorney General receives notification from the Secretary of Health and Human Services that the Secretary has approved an application under section 505(c), 512, or 571 of the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 355(c), 360b, 360ccc] or section 262(a) of title 42, or indexed a drug under section 572 of the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 360ccc–1], with respect to the drug described in paragraph (1).

(3) A rule issued by the Attorney General under paragraph (1) shall become immediately effective as an interim final rule without requiring the Attorney General to demonstrate good cause therefor. The interim final rule shall give interested persons the opportunity to comment and to request a hearing. After the conclusion of such proceedings, the Attorney General shall issue a final rule in accordance with the scheduling criteria of subsections (b), (c), and (d) of this section and section 812(b) of this title.

(Pub. L. 91–513, title II, §201, Oct. 27, 1970, 84 Stat. 1245; Pub. L. 95–633, title I, §102(a), Nov. 10, 1978, 92 Stat. 3769; Pub. L. 96–88, title V, §509(b), Oct. 17, 1979, 93 Stat. 695; Pub. L. 98–473, title II, §§508, 509(a), Oct. 12, 1984, 98 Stat. 2071, 2072; Pub. L. 108–358, §2(b), Oct. 22, 2004, 118 Stat. 1663; Pub. L. 112–144, title XI, §1153, July 9, 2012, 126 Stat. 1132; Pub. L. 113–260, §2(b), Dec. 18, 2014, 128 Stat. 2930; Pub. L. 114–89, §2(b), Nov. 25, 2015, 129 Stat. 700.)

REFERENCES IN TEXT

This subchapter, referred to in subsecs. (a), (c)(8), (d)(3), (4)(A), (B), and (g)(2), (3), was in the original "this title", meaning title II of Pub. L. 91–513, Oct. 27, 1970, 84 Stat. 1242, as amended, and is popularly known as the "Controlled Substances Act". For complete classification of title II to the Code, see second paragraph of Short Title note set out under section 801 of this title and Tables.

The Federal Food, Drug, and Cosmetic Act, referred to in subsecs. (d)(3) and (g)(1), is act June 25, 1938, ch. 675, 52 Stat. 1040, as amended, which is classified generally to chapter 9 (§301 et seq.) of this title. For complete classification of this Act to the Code, see section 301 of this title and Tables.

Schedules I, II, III, IV, and V, referred to in subsecs. (d)(4)(A), (B), (h)(1), and (j)(1), are set out in section 812(c) of this title.

The Psychotropic Substances Act of 1978, referred to in subsec. (d)(5), is Pub. L. 95–633, Nov. 10, 1978, 92 Stat. 3768, which enacted sections 801a, 830, and 852 of this title, amended sections 352, 802, 811, 812, 823, 827, 841 to 843, 872, 881, 952, 953, and 965 of this title and section 242a of Title 42, The Public Health and Welfare, repealed section 830 of this title effective Jan. 1, 1981, and enacted provisions set out as notes under sections 801, 801a, 812, and 830 of this title. For complete classification of this Act to the Code, see Short Title of 1978 Amendment note set out under section 801 of this title and Tables.

This subchapter and subchapter II of this chapter, referred to in subsec. (g)(1), was in the original "titles II and III of the Comprehensive Drug Abuse Prevention and Control Act", which was translated as meaning titles II and III of the Comprehensive Drug Abuse Prevention and Control Act of 1970, Pub. L. 91–513, Oct. 27, 1970, 84 Stat. 1242, 1285, as amended, to reflect the probable intent of Congress. Title II is classified principally to this subchapter and part A of title III comprises subchapter II of this chapter. For complete classification of this Act to the Code, see Short Title notes set out under section 801 of this title and Tables.

AMENDMENTS

2015—Subsec. (j). Pub. L. 114–89 added subsec. (j).

2014—Subsec. (i). Pub. L. 113–260 added subsec. (i).

2012—Subsec. (h)(2). Pub. L. 112–144 substituted "2 years" for "one year" and "1 year" for "six months".

2004—Subsec. (g)(1). Pub. L. 108–358, §2(b)(1), substituted "drug which contains a controlled substance from the application of this subchapter and subchapter II of this chapter if such drug" for "substance from a schedule if such substance".

Subsec. (g)(3)(C). Pub. L. 108–358, §2(b)(2), added subpar. (C).

1984—Subsec. (g)(3). Pub. L. 98–473, §509(a), added par. (3).

Subsec. (h). Pub. L. 98–473, §508, added subsec. (h).

1978—Subsec. (d). Pub. L. 95–633 designated existing provisions as par. (1) and added pars. (2) to (5).

CHANGE OF NAME

"Secretary of Health and Human Services" substituted for "Secretary of Health, Education, and Welfare" in subsec. (d)(2), (3), (4)(A), (B), (5) pursuant to section 509(b) of Pub. L. 96–88 which is classified to section 3508(b) of Title 20, Education.

EFFECTIVE DATE OF 2004 AMENDMENT

Amendment by Pub. L. 108–358 effective 90 days after Oct. 22, 2004, see section 2(d) of Pub. L. 108–358, set out as a note under section 802 of this title.

EFFECTIVE DATE OF 1978 AMENDMENT

Amendment by Pub. L. 95–633 effective on date the Convention on Psychotropic Substances enters into force in the United States [July 15, 1980], see section 112 of Pub. L. 95–633, set out as an Effective Date note under section 801a of this title.

nolu chan  posted on  2017-06-19   1:56:42 ET  Reply   Untrace   Trace   Private Reply  


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