Amphetamine, Methamphetamine, Fentanyl 49068 26 W M Pt

Total Page:16

File Type:pdf, Size:1020Kb

Amphetamine, Methamphetamine, Fentanyl 49068 26 W M Pt 2020 Annual2020 Annual ReportReport DDeeaatthhss rreellaatteedd ttoo ooppiioioiddss aanndd ootthheerr ddrruuggss CCaallhhoouunn This report is in memory of those who lost their life or a loved one to substance use. These losses must motivate us all to prevent future deaths. A few notes... Purpose: This data was collected by the Office of the Medical Examiner in the Department of Pathology at WMed. Unless otherwise noted, data is from 2020 and includes deaths where drugs were the immediate cause of death. This report is meant to provide up to date statistics to those involved in efforts to reduce the number of drug-related deaths. Sections with the following headings are approximations and frequencies may be higher than what is reported: Health Factors, Mental Health Factors, Social Factors, Children and Substance Use History. Sources: All data was extracted from a Medical Examiner database, law enforcement (LE) and EMS reports, death certificates, obituaries, Swift Toxicology of Overdose-Related Mortalities (STORM) results, medical records, toxicology reports, MDHHS reports, and autopsy reports. Please email Chloe Bielby for additional information or to set up a time to discuss your county's report: [email protected] Office of the Medical Examiner Annual 2020 Report Deaths Related to OCpalhiooiudns and Other Drugs All Drug-Related Deaths Injury Age Race Sex Death Certificate: Substances Contributing to Death Zip Code 18 W F Pt. I: Fentanyl, tramadol, cocaine, phentermine 49014 18 W M Pt. I: Amphetamine, methamphetamine, fentanyl 49068 26 W M Pt. I: Acetyl-fentanyl, amphetamine, fentanyl, xylazine 49015 26 W F Pt. I: Fentanyl, mitragynine, gabapentin, alprazolam 48917 28 W M Pt. I: Diazepam, alprazolam, olanzapine, quetiapine 49014 29 W M Pt. I: Fentanyl 49014 29 W F Pt. I: Methamphetamine, fentanyl, acetyl-fentanyl 49015 30 W F Pt. II: Morphine, buprenorphine, diphenhydramine, fentanyl* 49015 31 W M Pt. I: Fentanyl, heroin, ethanol 49015 32 W M Pt. I: Fentanyl, methamphetamine 49014 32 W M Pt. I: Fentanyl, methamphetamine, diphenhydramine 49037 33 W M Pt. I: Fentanyl 49017 33 B F Pt. I: Cocaine, ethanol, cocaethylene, methamphetamine, fentanyl, promethazine 49014 Pt. I: Acetyl-fentanyl, diphenhydramine, fentanyl, methamphetamine, 35 W F morphine, norbuprenorphine, xylazine 49015 35 W F Pt. II: Amphetamine, methamphetamine, fentanyl* 49015 35 W F Pt. I: Gabapentin, ketamine 49017 36 W F Pt. I: Methamphetamine 49015 37 W M Pt. I: Methamphetamine, fentanyl 49014 37 W M Pt. I: Fentanyl, heroin, methamphetamine 49015 38 W F Pt. I: Cocaine, methadone, tramadol, fentanyl 49014 38 W M Pt. I: Fentanyl, diphenhydramine 49015 40 W M Pt. I: Fentanyl, acetyl-fentanyl 49014 42 W M Pt. I: Fentanyl, clonazepam 49224 43 W F Pt. I: Cocaine, fentanyl, bupropion, gabapentin, trazodone 49014 43 W M Pt. I: Fentanyl, cocaine 49017 44 W M Pt. I: Heroin 49016 45 W M Pt. I: Dihydrocodeine, fentanyl, hydrocodone 49017 45 B M Pt. I: Fentanyl, heroin 49014 Office of the Medical Examiner Annual 2020 Report Deaths Related to OCpalhiooiudns and Other Drugs All Drug-Related Deaths (cont.) 45 W M Pt. I: Fentanyl, methamphetamine 49015 47 W F Pt. I: Alprazolam, gabapentin, promethazine, tramadol 49017 50 W M Pt. I: Ethanol, clonazepam, morphine, fentanyl 49014 52 W M Pt. I: Heroin, fentanyl, mitragynine, ethanol 49017 52 B F Pt. I: Cocaine Unknown 52 W M Pt. I: Methamphetamine, fentanyl, ethanol 49068 52 W M Pt. I: Methamphetamine, fentanyl 49014 54 W M Pt. I: Heroin, fentanyl, methamphetamine 49014 54 W M Pt. I: Fentanyl, clonazepam 49017 54 W M Pt. I: Morphine, amphetamine, fentanyl Unknown 55 B F Pt. I: Cocaine, codeine, fentanyl 49037 56 W F Pt. I: Fentanyl, heroin, amitriptyline 49037 56 W M Pt. I: Fentanyl, oxycodone, trazodone, promethazine 49068 57 W M Pt. I: Sertraline, tramadol, gabapentin, trazodone, diphenhydramine 49015 58 W M Pt. I: Fentanyl, acetyl-fentanyl, hydroxyzine, quetiapine, risperidone 49015 59 W F Pt. I: Fentanyl, oxycodone 49201 60 W M Pt. I: Cocaine, fentanyl, heroin, methamphetamine 49015 60 B M Pt. I: Cocaine, ethanol, fentanyl 49017 61 W M Pt. I: Fentanyl, mirtazapine 49017 62 W M Pt. I: Fentanyl, heroin, ethanol 49017 63 B M Pt. I: Cocaine, fentanyl, ethanol 49037 63 B M Pt. I: Cocaine 49017 65 B M Pt. I: Fentanyl, morphine, hydrocodone 49017 69 W M Pt. I: Cocaine 49015 70 W M Pt. I: Cocaine 49015 75 B M Pt. I: Methamphetamine, ethanol 49017 * Case is not included in the following report Office of the Medical Examiner Annual 2020 Report Deaths Related to OCpalhiooiudns and Other Drugs Total deaths due to drugs: 2018, 2019, 2020 2018 2019 2020 51 deaths 43 deaths 52 deaths 13 opioid only 8 opioid only 8 opioid only 4 non-opioid only 8 non-opioid only 8 non-opioid only 34 opioid & non-opioid 27 opioid & non-opioid 36 opioid & non-opioid 3.8 3.2 3.9 deaths per 10,000 deaths per 10,000 deaths per 10,000 Number of nonfatal overdoses among ED 568 41.7 Nonfatal overdoses discharges, 2020 per 10,000 Number of all drug-related deaths by month and year 9 8 8 8 7.5 7 6 6 6 6 6 6 y c 5 5 n e 5 u q 4 4 4 4 2018 e r F 2019 3 3 3 3 3 3 2020 2.5 2 2 2 2 2 1 0 0 l t r r r r ry ry h ri y e ly s e e e e a a rc p a n u u u u a M u J g b b b b n r A J u m to m m a b M A te c e e J e p O v c F e o e S N D Percent decrease Percent increase from 2018 to 2019 16% 21% from 2019 to 2020 Office of the Medical Examiner Annual 2020 Report DDeeaatthhss RReellaatteedd ttooG rOOaCpnpdaii lhoTorioiadudvnsesr saaenndd OOtthheerr DDrruuggss Demographics Decedent's Employment status Race Unemployed 31 Employed 11 Retired 4 Disability 3 Unknown 3 White (83%) African American/Black (17%) 0 5 10 15 20 25 30 Frequency County of Residence by County of Death Sex 46 25 73% 5 1 0 Decedent has residency in county of death Decedent did not have residency in county of death 27% Decedent was experiencing homelessness or insecure housing at time of death Decedent's Highest Level of Education Age 9th-12th grade, no diploma 9 Minimum Age High school graduate/GED 31 18 years Some college credit, no degree 9 Maximum Age Associates Degree 1 75 years Bachelors Degree 1 Masters Degree 1 Average Age 0 5 10 15 20 25 30 46 years Frequency Office of the Medical Examiner Annual 2020 Report DDeeaatthhss RReellaatteedd ttooG rOOaCpnpdaii lhoTorioiadudvnsesr saaenndd OOtthheerr DDrruuggss Health Factors Most prevalent ailments* Hypertension (31%) *Decedents may be represented in more than one category. Only illnesses with official diagnosis Chronic pain (21%) are included. **Lungs includes asthma, COPD, and emphysema Lungs** (17%) ***Heart includes MI, CABH, CAD, AFib, ACD, and heart failure Heart*** (12%) At least 9 decedents were Hepatitis C positive 7 of these decedents were known to use substances intravenously Body Mass Index (BMI) Decedent used Underweight 2 tobacco 71%+ Normal weight 13 Decedent Overweight 12 drank alcohol 54%+ Obese class 1 16 Obese class 2 8 Decedent had Obese class 3 1 a PCP 50% 0 5 10 15 Frequency Office of the Medical Examiner Annual 2020 Report DDeeaatthhss RReellaatteedd ttooG rOOaCpnpdaii lhoTorioiadudvnsesr saaenndd OOtthheerr DDrruuggss Mental Health Factors Most Depression (40%) prevalent mental illnesses* Bipolar (21%) *Decedents may be represented in more than one category. Anxiety (15%) Only mental illnesses with official diagnosis are included. PTSD (12%) Percentage of decedents... 19% 12% ...who have ever had ...with previous suicidal ideation suicide attempts Number Diagnosed Mental Illnesses among decedents 21 20 s t n 16 e d e c 15 e d g n o m a 10 y 8 c n e u q e 5 4 r F 3 0 0 1 2 3 4 Number of diagnosed mental illnesses Office of the Medical Examiner Annual 2020 Report DDeeaatthhss RReellaatteedd ttooG rOOaCpnpdaii lhoTorioiadudvnsesr saaenndd OOtthheerr DDrruuggss Social Factors Decedent was experiencing Decedent was 12% 10% homelessness or insecure a veteran housing at time of death 27% Decedent has ever 64% Decedents ever been incarcerated <60 incarcerated were released DAYS in past 60 days Children decedent had.... Number of Minor biological children Adult 1 minor 8 children 35% only 2 minors 3 At least 29% one minor 3 minors 3 child Unknown No 1 36% children 0 2 4 6 8 Frequency of decedents Employment status of those with minor children 4 decedents 27% 7% lived with Employed Disability their minor Unemployed Unknown child(ren) at time of death 67% 0% Office of the Medical Examiner Annual 2020 Report DDeeaatthhss RReellaatteedd ttooG rOOaCpnpdaii lhoTorioiadudvnsesr saaenndd OOtthheerr DDrruuggss Substance Use History At least 92% of At least 44% of those decedents were known decedents used to use or abuse substances substances intravenously At least 37% of At least 68% of those decedents have had at decedents have had least one two or more prior overdose prior overdoses At least 50% of At least 21% of decedents were decedents substance prescribed an opioid use started from the in the past two years prescribed opioid recovery history (n=48*) Decedent's substance of choice vs. what 40% Decedent has been to a was determined to cause death substance rehabilitation 22 clinic at least one time Cocaine 13 27 Decedent was currently Heroin 8% receiving or has received 9 a form of medication- 11 assisted treatment (MAT) Methamphetamine in the past two years 15 11 Other Opioids 40% Decedent was recently 65 substance free in the past three weeks Prescriptions 5 29 Suspected reasons for relapse** Other 1 18 0 20 40 60 53% 31% 16% Left jail/rehab Life stress*** Unknown Substance of Substance determined *ONLY decedents known to use substances are choice to cause death included.
Recommended publications
  • Effect of Intranasal Ketamine Vs Fentanyl on Pain
    1 PROTOCOL SYNOPSIS 2 STUDY TITLE: 3 Pain Reduction with Intranasal Medications for Extremity Injuries (PRIME): A Randomized Clinical 4 Noninferiority Trial of Intranasal Ketamine vs. Fentanyl 5 6 PROTOCOL TITLE 7 Pain Reduction with Intranasal Medications for Extremity injuries (PRIME) 8 9 PRINCIPAL INVESTIGATOR: 10 Theresa M. Frey, MD 11 Assistant Professor Clinical Pediatrics 12 Division of Pediatric Emergency Medicine 13 Cincinnati Children’s Hospital Medical Center 14 513-636-7966 15 [email protected] 16 17 CO-INVESTIGATORS: 18 Matthew R. Mittiga, MD 19 Todd A. Florin, MD, MSCE 20 Michelle C. Caruso, PharmD, BCPS 21 Nanhua Zhang, PhD 22 Yin Zhang, MS 23 24 I. ABSTRACT 25 26 Introduction: Inadequate pain control in the emergency department, particularly in the pediatric 27 population, is a major health concern. The intranasal route of medication administration is gaining 28 popularity secondary to its rapid onset of action, minimal discomfort for the patient and relative 29 simplicity. When pediatric patients present with moderate to severe pain from traumatic injuries, 30 opioids are currently the most frequently used class of analgesia, but they may not always be the best 31 option for numerous reasons. Sub-dissociative dosing of ketamine has been shown to be an effective 32 alternative to opioids in providing adequate pain relief. 33 34 Objectives: The objectives of this study are to 1) determine if intranasal ketamine is non-inferior to 35 intranasal fentanyl in reduction of pain in children presenting with extremity injuries and 2) define and 36 compare the level of sedation and respiratory side effect profile associated with intranasal ketamine and 37 fentanyl.
    [Show full text]
  • Guidelines for the Forensic Analysis of Drugs Facilitating Sexual Assault and Other Criminal Acts
    Vienna International Centre, PO Box 500, 1400 Vienna, Austria Tel.: (+43-1) 26060-0, Fax: (+43-1) 26060-5866, www.unodc.org Guidelines for the Forensic analysis of drugs facilitating sexual assault and other criminal acts United Nations publication Printed in Austria ST/NAR/45 *1186331*V.11-86331—December 2011 —300 Photo credits: UNODC Photo Library, iStock.com/Abel Mitja Varela Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Guidelines for the forensic analysis of drugs facilitating sexual assault and other criminal acts UNITED NATIONS New York, 2011 ST/NAR/45 © United Nations, December 2011. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. List of abbreviations . v Acknowledgements .......................................... vii 1. Introduction............................................. 1 1.1. Background ........................................ 1 1.2. Purpose and scope of the manual ...................... 2 2. Investigative and analytical challenges ....................... 5 3 Evidence collection ...................................... 9 3.1. Evidence collection kits .............................. 9 3.2. Sample transfer and storage........................... 10 3.3. Biological samples and sampling ...................... 11 3.4. Other samples ...................................... 12 4. Analytical considerations .................................. 13 4.1. Substances encountered in DFSA and other DFC cases .... 13 4.2. Procedures and analytical strategy...................... 14 4.3. Analytical methodology .............................. 15 4.4.
    [Show full text]
  • Biased Versus Partial Agonism in the Search for Safer Opioid Analgesics
    molecules Review Biased versus Partial Agonism in the Search for Safer Opioid Analgesics Joaquim Azevedo Neto 1 , Anna Costanzini 2 , Roberto De Giorgio 2 , David G. Lambert 3 , Chiara Ruzza 1,4,* and Girolamo Calò 1 1 Department of Biomedical and Specialty Surgical Sciences, Section of Pharmacology, University of Ferrara, 44121 Ferrara, Italy; [email protected] (J.A.N.); [email protected] (G.C.) 2 Department of Morphology, Surgery, Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy; [email protected] (A.C.); [email protected] (R.D.G.) 3 Department of Cardiovascular Sciences, Anesthesia, Critical Care and Pain Management, University of Leicester, Leicester LE1 7RH, UK; [email protected] 4 Technopole of Ferrara, LTTA Laboratory for Advanced Therapies, 44122 Ferrara, Italy * Correspondence: [email protected] Academic Editor: Helmut Schmidhammer Received: 23 July 2020; Accepted: 23 August 2020; Published: 25 August 2020 Abstract: Opioids such as morphine—acting at the mu opioid receptor—are the mainstay for treatment of moderate to severe pain and have good efficacy in these indications. However, these drugs produce a plethora of unwanted adverse effects including respiratory depression, constipation, immune suppression and with prolonged treatment, tolerance, dependence and abuse liability. Studies in β-arrestin 2 gene knockout (βarr2( / )) animals indicate that morphine analgesia is potentiated − − while side effects are reduced, suggesting that drugs biased away from arrestin may manifest with a reduced-side-effect profile. However, there is controversy in this area with improvement of morphine-induced constipation and reduced respiratory effects in βarr2( / ) mice. Moreover, − − studies performed with mice genetically engineered with G-protein-biased mu receptors suggested increased sensitivity of these animals to both analgesic actions and side effects of opioid drugs.
    [Show full text]
  • Product List March 2019 - Page 1 of 53
    Wessex has been sourcing and supplying active substances to medicine manufacturers since its incorporation in 1994. We supply from known, trusted partners working to full cGMP and with full regulatory support. Please contact us for details of the following products. Product CAS No. ( R)-2-Methyl-CBS-oxazaborolidine 112022-83-0 (-) (1R) Menthyl Chloroformate 14602-86-9 (+)-Sotalol Hydrochloride 959-24-0 (2R)-2-[(4-Ethyl-2, 3-dioxopiperazinyl) carbonylamino]-2-phenylacetic 63422-71-9 acid (2R)-2-[(4-Ethyl-2-3-dioxopiperazinyl) carbonylamino]-2-(4- 62893-24-7 hydroxyphenyl) acetic acid (r)-(+)-α-Lipoic Acid 1200-22-2 (S)-1-(2-Chloroacetyl) pyrrolidine-2-carbonitrile 207557-35-5 1,1'-Carbonyl diimidazole 530-62-1 1,3-Cyclohexanedione 504-02-9 1-[2-amino-1-(4-methoxyphenyl) ethyl] cyclohexanol acetate 839705-03-2 1-[2-Amino-1-(4-methoxyphenyl) ethyl] cyclohexanol Hydrochloride 130198-05-9 1-[Cyano-(4-methoxyphenyl) methyl] cyclohexanol 93413-76-4 1-Chloroethyl-4-nitrophenyl carbonate 101623-69-2 2-(2-Aminothiazol-4-yl) acetic acid Hydrochloride 66659-20-9 2-(4-Nitrophenyl)ethanamine Hydrochloride 29968-78-3 2,4 Dichlorobenzyl Alcohol (2,4 DCBA) 1777-82-8 2,6-Dichlorophenol 87-65-0 2.6 Diamino Pyridine 136-40-3 2-Aminoheptane Sulfate 6411-75-2 2-Ethylhexanoyl Chloride 760-67-8 2-Ethylhexyl Chloroformate 24468-13-1 2-Isopropyl-4-(N-methylaminomethyl) thiazole Hydrochloride 908591-25-3 4,4,4-Trifluoro-1-(4-methylphenyl)-1,3-butane dione 720-94-5 4,5,6,7-Tetrahydrothieno[3,2,c] pyridine Hydrochloride 28783-41-7 4-Chloro-N-methyl-piperidine 5570-77-4
    [Show full text]
  • Slang Terms and Code Words: a Reference for Law Enforcement
    UNCLASSIFIED Slang Terms and Code Words: A Reference for Law DEA Enforcement Personnel Intelligence DEA-HOU-DIR-022-18 July 2018 ReportBrief 1 UNCLASSIFIED UNCLASSIFIED DEA Intelligence Report Executive Summary This Drug Enforcement Administration (DEA) Intelligence Report contains new and updated information on slang terms and code words from a variety of law enforcement and open sources, and serves as an updated version to the product entitled “Drug Slang Code Words” published by the DEA in May 2017. It is designed as a ready reference for law enforcement personnel who are confronted with hundreds of slang terms and code words used to identify a wide variety of controlled substances, designer drugs, synthetic compounds, measurements, locations, weapons, and other miscellaneous terms relevant to the drug trade. Although every effort was made to ensure the accuracy and completeness of the information presented, due to the dynamics of the ever-changing drug scene, subsequent additions, deletions, and corrections are inevitable. Future addendums and updates to this report will attempt to capture changed terminology to the furthest extent possible. This compendium of slang terms and code words is alphabetically ordered, with new additions presented in italic text, and identifies drugs and drug categories in English and foreign language derivations. Drug Slang Terms and Code Wordsa Acetaminophen and Oxycodone Combination (Percocet®) 512s; Bananas; Blue; Blue Dynamite; Blueberries; Buttons; Ercs; Greenies; Hillbilly Heroin; Kickers; M-30s;
    [Show full text]
  • (19) United States (12) Patent Application Publication (10) Pub
    US 20130289061A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2013/0289061 A1 Bhide et al. (43) Pub. Date: Oct. 31, 2013 (54) METHODS AND COMPOSITIONS TO Publication Classi?cation PREVENT ADDICTION (51) Int. Cl. (71) Applicant: The General Hospital Corporation, A61K 31/485 (2006-01) Boston’ MA (Us) A61K 31/4458 (2006.01) (52) U.S. Cl. (72) Inventors: Pradeep G. Bhide; Peabody, MA (US); CPC """"" " A61K31/485 (201301); ‘4161223011? Jmm‘“ Zhu’ Ansm’ MA. (Us); USPC ......... .. 514/282; 514/317; 514/654; 514/618; Thomas J. Spencer; Carhsle; MA (US); 514/279 Joseph Biederman; Brookline; MA (Us) (57) ABSTRACT Disclosed herein is a method of reducing or preventing the development of aversion to a CNS stimulant in a subject (21) App1_ NO_; 13/924,815 comprising; administering a therapeutic amount of the neu rological stimulant and administering an antagonist of the kappa opioid receptor; to thereby reduce or prevent the devel - . opment of aversion to the CNS stimulant in the subject. Also (22) Flled' Jun‘ 24’ 2013 disclosed is a method of reducing or preventing the develop ment of addiction to a CNS stimulant in a subj ect; comprising; _ _ administering the CNS stimulant and administering a mu Related U‘s‘ Apphcatlon Data opioid receptor antagonist to thereby reduce or prevent the (63) Continuation of application NO 13/389,959, ?led on development of addiction to the CNS stimulant in the subject. Apt 27’ 2012’ ?led as application NO_ PCT/US2010/ Also disclosed are pharmaceutical compositions comprising 045486 on Aug' 13 2010' a central nervous system stimulant and an opioid receptor ’ antagonist.
    [Show full text]
  • Opioid Receptorsreceptors
    OPIOIDOPIOID RECEPTORSRECEPTORS defined or “classical” types of opioid receptor µ,dk and . Alistair Corbett, Sandy McKnight and Graeme Genes encoding for these receptors have been cloned.5, Henderson 6,7,8 More recently, cDNA encoding an “orphan” receptor Dr Alistair Corbett is Lecturer in the School of was identified which has a high degree of homology to Biological and Biomedical Sciences, Glasgow the “classical” opioid receptors; on structural grounds Caledonian University, Cowcaddens Road, this receptor is an opioid receptor and has been named Glasgow G4 0BA, UK. ORL (opioid receptor-like).9 As would be predicted from 1 Dr Sandy McKnight is Associate Director, Parke- their known abilities to couple through pertussis toxin- Davis Neuroscience Research Centre, sensitive G-proteins, all of the cloned opioid receptors Cambridge University Forvie Site, Robinson possess the same general structure of an extracellular Way, Cambridge CB2 2QB, UK. N-terminal region, seven transmembrane domains and Professor Graeme Henderson is Professor of intracellular C-terminal tail structure. There is Pharmacology and Head of Department, pharmacological evidence for subtypes of each Department of Pharmacology, School of Medical receptor and other types of novel, less well- Sciences, University of Bristol, University Walk, characterised opioid receptors,eliz , , , , have also been Bristol BS8 1TD, UK. postulated. Thes -receptor, however, is no longer regarded as an opioid receptor. Introduction Receptor Subtypes Preparations of the opium poppy papaver somniferum m-Receptor subtypes have been used for many hundreds of years to relieve The MOR-1 gene, encoding for one form of them - pain. In 1803, Sertürner isolated a crystalline sample of receptor, shows approximately 50-70% homology to the main constituent alkaloid, morphine, which was later shown to be almost entirely responsible for the the genes encoding for thedk -(DOR-1), -(KOR-1) and orphan (ORL ) receptors.
    [Show full text]
  • Examination of Antimicrobial Activity of Selected Non-Antibiotic Medicinal Preparations
    Acta Poloniae Pharmaceutica ñ Drug Research, Vol. 69 No. 6 pp.1368ñ1371, 2012 ISSN 0001-6837 Polish Pharmaceutical Society EXAMINATION OF ANTIMICROBIAL ACTIVITY OF SELECTED NON-ANTIBIOTIC MEDICINAL PREPARATIONS HANNA KRUSZEWSKA1*, TOMASZ ZAR BA1 and STEFAN TYSKI1,2 1National Medicines Institute, Department of Antibiotics and Microbiology, 30-34 Che≥mska St., 00-725 Warszawa, Poland 2 Medical University of Warsaw, Department of Pharmaceutical Microbiology, 3 Oczki St., 02-007 Warszawa, Poland Abstract: The aim of this study was to detect and characterize the antimicrobial activity of non-antibiotic drugs, selected from the pharmaceutical products analyzed during the state control performed in National Medicines Institute, Warszawa, Poland. In 2010, over 90 pharmaceutical preparations have been randomly chosen from different groups of drugs. The surveillance study was performed on standard ATCC microbial strains used for drug control: S. aureus, E. coli, P. aeruginosa and C. albicans. It was shown that the drugs listed below inhib- ited growth of at least one of the examined strains: Arketis 20 mg tab. (paroxetine), Buvasodil 150 mg tab. (buflomedile), Halidor 100 mg tab. (bencyclane), Hydroxyzinum espefa 25 mg tab. (hydroxyzine), Norifaz 35 mg tab. (risedronate), Strattera 60 mg cap. (atomoxetine), Tamiflu 75 mg tab. (oseltamivir), Valpro-ratiopharm Chrono 300 mg tab. with longer dissolution (valproate), Vetminth oral paste 24 g+3 g/100 mL (niclozamide, oxybendazol). Strattera cap. showed broad activity spectrum. It inhibited growth of
    [Show full text]
  • Recommended Methods for the Identification and Analysis of Fentanyl and Its Analogues in Biological Specimens
    Recommended methods for the Identification and Analysis of Fentanyl and its Analogues in Biological Specimens MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Recommended Methods for the Identification and Analysis of Fentanyl and its Analogues in Biological Specimens MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES UNITED NATIONS Vienna, 2017 Note Operating and experimental conditions are reproduced from the original reference materials, including unpublished methods, validated and used in selected national laboratories as per the list of references. A number of alternative conditions and substitution of named commercial products may provide comparable results in many cases. However, any modification has to be validated before it is integrated into laboratory routines. ST/NAR/53 Original language: English © United Nations, November 2017. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. Mention of names of firms and commercial products does not imply the endorse- ment of the United Nations. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. Acknowledgements The Laboratory and Scientific Section of the UNODC (LSS, headed by Dr. Justice Tettey) wishes to express its appreciation and thanks to Dr. Barry Logan, Center for Forensic Science Research and Education, at the Fredric Rieders Family Founda- tion and NMS Labs, United States; Amanda L.A.
    [Show full text]
  • Fentanyl Infographic 24X36
    FENTANYL WHAT IS IT? Fentanyl can be found in prescription form, introduced to the medical community in the 1960s Fentanyl analogues are now being Fentanyl is a potent synthetic and prescribed to relieve severe pain post-surgery created in clandestine laboratories to opioid analgesic, 50 to 100x or during end-of-life care . In its prescription form, be sold and used illegally. In it's non- more powerful than fentanyl is sold under the brand names Actiq®, prescription form, fentanyl is found in morphine. Duragesic®, and Sublimaze®. When prescribed by a powder form, spiked on blotter paper; physician, fentanyl is often administered via mixed with heroin; or as tablets that injection, transdermal patch, or in lozenges. attempt to mimic other opioids. Effects: Like other opioids, Fentanyl binds to Through Fentanyl's effects on the Euphoria, relaxation, drowsiness, opioid receptors in the reward centers opioid receptors in the brain stem nausea, confusion, constipation, of the brain, increasing dopamine however, it can inhibit normal sedation, tolerance, addiction, levels to cause a surge in endorphins breathing, causing breathing to stop respiratory depression and arrest, and feelings of pleasure. altogether, leading to death. unconsciousness, coma, and death. WHY DOES IT MATTER? 540% While the fast-acting nature of the effects of fentanyl may create a more powerful and immediate euphoria, these increase in fentanyl effects wear off faster, leading to the more immediate return overdose deaths of cravings and discomfort. since 2016 (CDC) With a high profit margin, Fentanyl is often mixed into heroin or is made to mimic the In talking about Fentanyl, you may hear about appearance of other opioids.
    [Show full text]
  • Toxicology Cases: 10 Must-Have Drugs to Keep on Hand
    Toxicology Cases: 10 Must-Have Drugs To Keep On Hand Acepromazine Atipamezole Cholestyramine Cyproheptadine Diazepam/ Midazolam Used in animals as a Commonly used to Useful for several Should be an additional For controlling mild sedative; much higher reverse dexmedetomidine toxins that undergo treatment for overdoses agitation or seizures from doses than normal may and xylazine. enterohepatic of serotonergic a variety of toxins. be needed when dealing Note: Can reverse recirculation: drugs such as SSRIs, Note: Should not be with amphetamine signs from other cholecalciferol (vitamin amphetamines, tramadol, used for overdoses of toxicosis. alpha agonists such as D3), sago palm, 5-HTP and marijuana amphetamines as it can clonidine, guanfacine, actually worsen clinical Note: Can also be used to cyanobacteria (blue when signs persist despite tizanidine, imidazoline signs. Also contraindicated help control hypertension green algae), digitoxin treatment with first-line and oxymetazoline for seizures caused by caused by stimulants when and some NSAIDs. drugs. decongestants; eye drops, muscimol (isoxazole) nitroprusside is not available and tick collars that contain Note: Some human Note: Only administer while mushroom ingestions. – start with small doses amitraz. and titrate to affect. Always formulations contain xylitol signs of serotonin syndrome monitor blood pressure. and those must not be used are present – most toxicity in dogs. cases only require 1-3 doses. Maropitant Methocarbamol N-Acetylcysteine Naloxone Propranolol Very effective at both For patients presenting Commonly used for Along with reversing Primarily used to treat stopping and preventing with tremors instead acetaminophen toxicosis; opioid exposure, can be sinus tachycardia vomiting. of seizures. Though can be given along used to reverse severe from chocolate, Note: Administration in expensive, there is with SAMe for other CNS depression from amphetamines, SSRIs, recumbent or neurologic nothing that will control hepatotoxins.
    [Show full text]
  • Companion Animal Euthanasia Training Academy
    Companion Animal Euthanasia Training Academy Oral and Injectable Pre-Euthanasia Sedatives/Anesthetics for Dogs and Cats Compiled in 2017 by Dr. Kathleen Cooney, U.S. CAETA instructor Disclaimer: These protocols are meant to provide options for sedation or anesthesia, ranging from mild to deep planes of sleep. Intraorgan injections are only permissible during periods of heavy sedation or anesthesia wherein the animal is pain-free and unaware the injection is occurring. When in doubt, CAETA recommends more drug be given to ensure a pain-free death. Giving sedative or anesthetic drugs to frail and compromised animals can result in adverse reactions or death itself. Drug and drug combinations can be administered intramuscular(IM) or subcutaneous (SQ) unless otherwise specified. Oral drugs may not elicite the desired depth of sleep every time. Many factors affect rate of absorption and uptake. Higher doses may be given initially or when it becomes clear the pet requires more. Dr. Cooney’s Injectable Protocols (IM and SQ) Dogs Sedation protocol (SQ preferred) • Dexmedetomidine (0.5mg/ml) = 0.1 ml per 10# minus 0.1ml (can decrease total by 0.2mls over 50# bw) [can substitute with Xylazine (100mg/ml) = 0.1ml per 10#] • Nalbuphine (20mg/ml) = 0.1 ml per 10# or Butorphanol (10mg/ml) = 0.1 ml per 10# • Acepromazine (10mg/ml) = 0.05 ml per 10# Anesthesia protocol • Telazol® (100mg/ml) = 0.1 ml per 10# • Acepromazine (10mg/ml) = 0.1 ml per 10# • Xylazine (100mg/ml) = 0.025 ml per 10# Cats Anesthesia protocol • Telazol®* (100mg/ml) = 0.15 ml for 2-5# 0.25 ml for 5-10# 0.3 ml for 10+# • Acepromazine (10mg/ml) = 0.1 ml for all BW Anesthesia protocol • Alfaxalone (10mg/ml) = 1.1 -1.5ml for most cats • Nalbuphine (20mg/ml) = 0.2ml for all BW • Acepromazine (10mg/ml)=0.1ml for all BW BW = body weight # = pounds mg = milligram ml = milliliter Various Other Injectable Protocols Shared by Veterinary Colleagues, compiled in 2016 Dogs 1.
    [Show full text]