The Impact of Cannabis Access Laws on Opioid Prescribing
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Medications to Treat Opioid Use Disorder Research Report
Research Report Revised Junio 2018 Medications to Treat Opioid Use Disorder Research Report Table of Contents Medications to Treat Opioid Use Disorder Research Report Overview How do medications to treat opioid use disorder work? How effective are medications to treat opioid use disorder? What are misconceptions about maintenance treatment? What is the treatment need versus the diversion risk for opioid use disorder treatment? What is the impact of medication for opioid use disorder treatment on HIV/HCV outcomes? How is opioid use disorder treated in the criminal justice system? Is medication to treat opioid use disorder available in the military? What treatment is available for pregnant mothers and their babies? How much does opioid treatment cost? Is naloxone accessible? References Page 1 Medications to Treat Opioid Use Disorder Research Report Discusses effective medications used to treat opioid use disorders: methadone, buprenorphine, and naltrexone. Overview An estimated 1.4 million people in the United States had a substance use disorder related to prescription opioids in 2019.1 However, only a fraction of people with prescription opioid use disorders receive tailored treatment (22 percent in 2019).1 Overdose deaths involving prescription opioids more than quadrupled from 1999 through 2016 followed by significant declines reported in both 2018 and 2019.2,3 Besides overdose, consequences of the opioid crisis include a rising incidence of infants born dependent on opioids because their mothers used these substances during pregnancy4,5 and increased spread of infectious diseases, including HIV and hepatitis C (HCV), as was seen in 2015 in southern Indiana.6 Effective prevention and treatment strategies exist for opioid misuse and use disorder but are highly underutilized across the United States. -
The Opioid Epidemic: What Labs Have to Do with It?
The Opioid Epidemic: What labs have to do with it? Ewa King, Ph.D. Associate Director of Health RIDOH State Health Laboratories Analysis. Answers. Action. www.aphl.org Overview • Overdose trends • Opioids and their effects • Analytical testing approaches • Toxicology laboratories Analysis. Answers. Action. www.aphl.org Opioid overdose crisis 1 Analysis. Answers. Action. www.aphl.org Opioid overdose crisis 2 Analysis. Answers. Action. www.aphl.org Opiates and Opioids • Opiates vs. Opioids • Opiates: Naturally occurring, derived from the poppy plant • Opioids: “Opiate-like” drugs in effects, not chemical structure Includes opiates • Narcotic analgesics • CNS depressants • DEA Schedule I or II controlled substances • Additive effect with other CNS depressant drugs Analysis. Answers. Action. www.aphl.org Efficacy of Opioids • How do opioids work? • Bind with opioid receptors • Brain, spinal cord, GI tract, and throughout the body • Pain, emotion, breathing, movement, and digestion Opioid Receptor Analysis. Answers. Action. www.aphl.org Effects of Opioids Physiological Psychological • Pain relief • Drowsiness/ sedation • Cough suppression • Mental confusion • GI motility • Loss of memory • Respiratory depression • Lethargy/ apathy • Pupillary constriction • Euphoria/ tranquility • Itching • Mood swings • Constipation • Depression • Dependence • Withdrawal • Dependence Analysis. Answers. Action. www.aphl.org Opiates 1 Opiates • Naturally occurring alkaloids Opium • Latex from the opium poppy plant Codeine: • Mild to moderate pain • Antitussive Morphine: • Severe pain • Metabolite of codeine and heroin Analysis. Answers. Action. www.aphl.org Opiates 2 Semi-synthetic Opiates: • Synthesized from a natural opiate Heroin: • Schedule I narcotic Hydrocodone (Vicodin): • Mild to moderate pain • Metabolizes to hydromorphone (Dilaudid) Oxycodone (Oxycontin/Percocet): • Moderate to severe pain • Metabolizes to oxymorphone (Opana) Analysis. Answers. Action. -
Tobacco & Cannabis
TOBACCO & CANNABIS: THE EVOLUTION OF PERTINENT RULES & REGULATIONS AND SUBSEQUENT FINANCIAL RAMIFICATIONS by Virginia Palmer Yerger Avisto A thesis submitted to the faculty of The University of Mississippi in partial fulfillment of the requirements of the Sally McDonnell Barksdale Honors College. Oxford May 2016 Approved by _________________________ Advisor: Dr. Bonnie Van Ness _________________________ Reader: Dr. Travis Box _________________________ Reader: Dr. Dwight Frink © 2016 Virginia Palmer Yerger Avisto ALL RIGHTS RESERVED ii I would like to dedicate my thesis to all family members who encouraged me to apply to the Honors College and acted as my cheerleaders throughout the entire process. Peter Avisto Virginia Avisto Harrison Avisto Gingia Yerger Swan Yerger Patricia Avisto Uno Avisto iii ABSTRACT PALMER AVISTO: Tobacco & Cannabis: The Evolution of Pertinent Rules & Regulations and Subsequent Financial Ramifications (Under the direction of Dr. Bonnie Van Ness) My thesis will discuss the evolution of the regulations surrounding tobacco and cannabis and the subsequent financial ramifications later posed on pertaining companies and the industries themselves. I will also briefly discuss the evolution of tobacco advertisements and the introduction of e-cigarettes into the tobacco market. Concerning newly legalized cannabis stores, I will discuss the struggle to acquire financial tools, the state-Federal disagreement, and proposed solutions to those issues. Both having been deemed “public enemy number one,” I will compare marijuana and tobacco regarding health effects, profitability after new laws, and their overall economic profitability for the country. I researched and summarized all pertinent regulations for the two industries and analyzed the available annual reports for the major tobacco companies. -
The Opioid Crisis and the Black/African American Population: an Urgent Issue
THE OPIOID CRISIS AND THE BLACK/AFRICAN AMERICAN POPULATION: AN URGENT ISSUE THE OPIOID CRISIS AND THE BLACK/AFRICAN AMERICAN POPULATION: AN URGENT ISSUE U.S. Department of Health and Human Services Substance Abuse and Mental Health Services Administration Office of Behavioral Health Equity Table of Contents Introduction ...................................................................................................................................................... 3 i. Purpose of the Issue Brief ........................................................................................................................ 3 ii. Sources of Information ............................................................................................................................ 4 Opioids in Black/African American Communities: Context .................................................................. 4 i. What Do the National Data Show? ........................................................................................................ 4 ii. Routes to Opioid Misuse and Overdose Deaths: Pain Management, Illicit Drug Use, and Opioid Comorbidities in Black/African American Communities .................................................... 6 iii. Challenges to Prevention, Treatment, and Recovery .......................................................................... 7 Strategies to Address Opioid Misuse and OUD in Black/African American Communities ............ 9 i. Standard Treatment ................................................................................................................................ -
Phencyclidine: an Update
Phencyclidine: An Update U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES • Public Health Service • Alcohol, Drug Abuse and Mental Health Administration Phencyclidine: An Update Editor: Doris H. Clouet, Ph.D. Division of Preclinical Research National Institute on Drug Abuse and New York State Division of Substance Abuse Services NIDA Research Monograph 64 1986 DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Alcohol, Drug Abuse, and Mental Health Administratlon National Institute on Drug Abuse 5600 Fishers Lane Rockville, Maryland 20657 For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, DC 20402 NIDA Research Monographs are prepared by the research divisions of the National lnstitute on Drug Abuse and published by its Office of Science The primary objective of the series is to provide critical reviews of research problem areas and techniques, the content of state-of-the-art conferences, and integrative research reviews. its dual publication emphasis is rapid and targeted dissemination to the scientific and professional community. Editorial Advisors MARTIN W. ADLER, Ph.D. SIDNEY COHEN, M.D. Temple University School of Medicine Los Angeles, California Philadelphia, Pennsylvania SYDNEY ARCHER, Ph.D. MARY L. JACOBSON Rensselaer Polytechnic lnstitute National Federation of Parents for Troy, New York Drug Free Youth RICHARD E. BELLEVILLE, Ph.D. Omaha, Nebraska NB Associates, Health Sciences Rockville, Maryland REESE T. JONES, M.D. KARST J. BESTEMAN Langley Porter Neuropsychiatric lnstitute Alcohol and Drug Problems Association San Francisco, California of North America Washington, D.C. DENISE KANDEL, Ph.D GILBERT J. BOTV N, Ph.D. College of Physicians and Surgeons of Cornell University Medical College Columbia University New York, New York New York, New York JOSEPH V. -
Dextrorphan Binds to Opioid Receptors in Guinea-Pig Brain Membranes And
Proc. Natl. Acad. Sci. USA Vol. 87, pp. 1629-1632, March 1990 Pharmacology Dextrorphan binds to opioid receptors in guinea-pig brain membranes and is an antagonist at opioid receptors in myenteric plexus (binding/guinea-pig ileum/levorphanol/stereoselectivity) AVRAM GOLDSTEIN AND ASHA NAIDU Department of Pharmacology, Stanford University, Stanford, CA 94305 Contributed by Avram Goldstein, December 11, 1989 ABSTRACT Dextrorphan (+)-tartrate, purified by re- LaRoche); [D-Ala,MePhe4,Gly-ol5]enkephalin (DAGO; Pe- peated crystallization to remove all traces of the enantiomer ninsula Laboratories) (2); trans-3,4-dichloro-N-methyl- levorphanol, binds to IL, 6, and K sites on guinea-pig brain N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide methane- membranes with lower affinities (by a factor of400-3200) than sulfonate (U50,488; Upjohn) (3); (-)-naloxone hydrochloride levorphanol. In the guinea-pig ileum myenteric plexus longi- (NAL; Endo Laboratories, New York); normorphine hydro- tudinal muscle preparation (GPI), dextrorphan, at 100-200 chloride (NOR) and (+)-naloxone hydrochloride (National ,uM, inhibits the electrically stimulated twitch, but this action Institute on Drug Abuse); N-methyl-D-aspartic acid (NMDA), is not blocked or reversed by naloxone; both (+)- and (-)- aminophosphonovalerate, norepinephrine (levarterenol), at- naloxone produce similar non-opioid twitch inhibition at com- ropine, and eserine (physostigmine) (Sigma). parable concentrations. At 10-20 jaM, dextrorphan' blocks and Preparation ofDEXp. [3H]LEV (Ro 1-5431/701, Hoffmann- reverses the twitch inhibition due to ,u and KWagonists, but the LaRoche; 17.4 Ci/mmol; 1 Ci = 37 GBq) was purified' by blockade can be overcome only partially by increasing the preparative reversed-phase HPLC (Waters, C18 AgBondaPak, agonist concentration. -
The Forensic Identification of Marijuana: Suspicion, Moral Danger, and the Creation Of
Title: The Forensic Identification of Marijuana: Suspicion, Moral Danger, and the Creation of Non-Psychoactive THC Author: Aaron Roussell* Running Head: “Marijuana Identification” Abstract: Federal and state laws present marijuana as a dangerous substance requiring coercive control and forbid private citizens from possessing, selling, or growing it. Possession cases brought under these laws depend on a forensic confirmation of taxonomic identity as Cannabis sativa to establish and successfully prosecute a case. Hemp Industries Association v. DEA (2003), a recent federal appeals court ruling, is at odds with this forensic process. American citizens may legally possess and even consume a similar substance — hemp and its derivatives — which can be made into such everyday objects as clothing, rope, and food products. Yet these two plants are both Cannabis sativa and differ only in physical structure and degree of natural tetrahydrocannabinol (THC). Synthetic THC is also a medically prescribed substance, which introduces further confusion into the legal standing of cannabis. Finally, *Department of Criminology, Law & Society, University of California, Irvine. Address correspondence to Aaron Roussell, Department of Criminology, Law & Society, University of California, Irvine, Social Ecology II, Irvine, CA 92697; email: [email protected]. 949-943-9860 Thanks to Professors Simon Cole, Justin Richland, Michael Clegg, and Dr. Fred Whitehurst for their direct or indirect contributions and assistance, as well as Akhila Ananth, Vivek Mittal, and Trish Goforth for their help with paper drafts and the editorial staff of the Albany Law Journal of Science and Technology for their superb efforts to improve the final version. Mistakes and weaknesses herein are entirely in spite of their efforts and remain the sole dominion of the author. -
(Oxycodone) RATIONALE for INCLUSION in PA PROGRAM
OXYCODONE IR (oxycodone) RATIONALE FOR INCLUSION IN PA PROGRAM Background Oxycodone hydrochloride, a pure opioid agonist, is used in the treatment of moderate to severe pain (1-2). The precise mechanism of action is unknown; however, specific opioid receptors in the CNS have been identified and are considered to play a role in the therapeutic effects of the drug (3). Oxycodone is a Schedule II controlled substance and can be abused in a manner similar to other opioid agonists, legal or illicit. This should be considered when prescribing or dispensing oxycodone in a situation where misuse, abuse, or diversion are a concern (1). Regulatory Status FDA-approved indications: Oxycodone IR tablets and capsules are immediate-release (IR) oral formulations of oxycodone hydrochloride indicated for the management of moderate to severe pain where the use of an opioid analgesic is appropriate. Oxycodone hydrochloride oral solution 100 mg/5 mL (20 mg/mL) is an opioid analgesic indicated for the management of moderate to severe acute and chronic pain in opioid-tolerant patients (1-3). Limitations of use: (1) Because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses, reserve Oxycodone IR for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or non-opioid combination products): • Have not been tolerated, or are not expected to be tolerated • Have not provided adequate analgesia or are not expected to provide adequate analgesia The Oxycodone IR has boxed warnings for the following (1-6): • Respiratory depression is the chief hazard of opioid agonists, including morphine sulfate, which if not immediately recognized and treated, may lead to respiratory arrest and death. -
Benefit/Risk Assessment of Prescription Opioid Antitussive Products for Treatment of Cough in Pediatric Patients
Background Document Pediatric Advisory Committee Meeting September 11, 2017 Benefit/Risk Assessment of Prescription Opioid Antitussive Products for Treatment of Cough in Pediatric Patients Table of Contents 1. Introduction ..........................................................................................................................................2 2. Regulatory History of Prescription Opioid Antitussive Products .......................................................... 3 Codeine ..................................................................................................................................................... 3 Hydrocodone............................................................................................................................................. 5 Pediatric Study Requirements for Prescription Opioid Antitussives ........................................................ 8 3. Safety of Opioid Antitussive Products among Children and Adolescents ............................................ 9 Codeine and Risk of Respiratory Depression and Death Due to Ultra‐rapid Metabolism........................9 Hydrocodone and Risk of Respiratory Depression and Death................................................................ 12 Risks of misuse, abuse, addiction, overdose and death with opioid antitussives .................................. 13 4. Utilization of Products to Treat Cough in Pediatric Patients .............................................................. 14 5. Treatment Alternatives for Cough -
OXYCODONE (Trade Names: Tylox®, Percodan®, Oxycontin®) March 2020
Drug Enforcement Administration Diversion Control Division Drug & Chemical Evaluation Section OXYCODONE (Trade Names: Tylox®, Percodan®, OxyContin®) March 2020 Introduction: abusers and doctor-shoppers. They are abused either as intact Oxycodone is a schedule II narcotic analgesic and is widely tablets or by crushing or chewing the tablet and then swallowing, used in clinical medicine. It is marketed either alone as controlled snorting or injecting. Products containing oxycodone in combination release (OxyContin®) and immediate release formulations (OxyIR®, with acetaminophen or aspirin are abused orally. Acetaminophen OxyFast®), or in combination with other nonnarcotic analgesics present in the combination products poses an additional risk of liver such as aspirin (Percodan®) or acetaminophen (Percocet®). In toxicity upon chronic abuse. 2004, the Food and Drug Administration (FDA) approved generic The National Survey on Drug Use and Health (NSDUH) forms of controlled release oxycodone products for marketing. The indicated that among the 27.9 million people, aged 12 and older in introduction in 1996 of OxyContin®, commonly known on the street the U.S. that reported using oxycodone products in 2015, 4.3 million as OC, OX, Oxy, Oxycotton, Hillbilly heroin, and kicker, led to a (15.2%) misused the products. In 2016, a decrease was observed marked escalation of its abuse as reported by drug abuse treatment among the 27.6 million users, aged 12 years and older within the centers, law enforcement personnel, and health care professionals. U.S., in which 3.9 million (14.1%) misused oxycodone products. For Although the diversion and abuse of OxyContin® appeared initially 2017, the decrease continued among the 26.7 million users, aged in the eastern U.S., it has now spread to the western U.S. -
OXYCONTIN® (Oxycodone Hydrochloride)
Medication Guide OXYCONTIN® (ox-e-KON-tin) (oxycodone hydrochloride) extended-release tablets, CII OXYCONTIN is: • A strong prescription pain medicine that contains an opioid (narcotic) that is used to manage pain severe enough to require daily around-the-clock, long-term treatment with an opioid, when other pain treatments such as non-opioid pain medicines or immediate-release opioid medicines do not treat your pain well enough or you cannot tolerate them. • A long-acting (extended-release) opioid pain medicine that can put you at risk for overdose and death. Even if you take your dose correctly as prescribed you are at risk for opioid addiction, abuse, and misuse that can lead to death. • Not for use to treat pain that is not around-the-clock. • Not for use in children less than 11 years of age and who are not already using opioid pain medicines regularly to manage pain severe enough to require daily around-the-clock long-term treatment of pain with an opioid . Important information about OXYCONTIN: • Get emergency help right away if you take too much OXYCONTIN (overdose). When you first start taking OXYCONTIN, when your dose is changed, or if you take too much (overdose), serious or life-threatening breathing problems that can lead to death may occur. • Never give anyone else your OXYCONTIN. They could die from taking it. Store OXYCONTIN away from children and in a safe place to prevent stealing or abuse. Selling or giving away OXYCONTIN is against the law. Do not take OXYCONTIN if you have: • severe asthma, trouble breathing, or other lung problems. -
Investing in the Legal U.S. Cannabis Market
INVESTING IN THE LEGAL U.S. CANNABIS MARKET WHITE PAPER OCTOBER 2019 PETE KARABAS • TIBY ERDELY • JORDAN YOUKILIS FOUNDING PARTNERS OF KEY INVESTMENT PARTNERS LLC P a g e | 1 Table of contents Executive summary .............................................................................................................................................................................. 2 Section 1: Cannabis 101 ........................................................................................................................................................................ 3 Section 2: Projected growth of the cannabis market ..................................................................................................................... 7 Section 3: The politics of cannabis in the U.S. .............................................................................................................................. 11 Section 4: Unique characteristics of the cannabis industry as an investment opportunity ............................................... 16 Section 5: The public cannabis markets ......................................................................................................................................... 19 Section 6: Investors in ancillary businesses can avoid several risks that plant-touching investors will face today .... 23 Section 7: Conclusion .........................................................................................................................................................................