DEA-Drugs of Abuse
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Zoletil 100 Injectable Anaesthetic/Sedative for Dogs, Cats, Zoo and Wild Animals
Zoletil 100 Injectable Anaesthetic/Sedative for Dogs, Cats, Zoo and Wild Animals Virbac (Australia) Pty Limited Chemwatch Hazard Alert Code: 1 Chemwatch: 6978267 Issue Date: 11/01/2019 Version No: 4.1.16.10 Print Date: 08/31/2021 Safety Data Sheet according to WHS Regulations (Hazardous Chemicals) Amendment 2020 and ADG requirements L.GHS.AUS.EN SECTION 1 Identification of the substance / mixture and of the company / undertaking Product Identifier Product name Zoletil 100 Injectable Anaesthetic/Sedative for Dogs, Cats, Zoo and Wild Animals Chemical Name Not Applicable Synonyms APVMA No.: 38837 Chemical formula Not Applicable Other means of identification Not Available Relevant identified uses of the substance or mixture and uses advised against Relevant identified uses For the anaesthesia and immobilisation of dogs, cats, zoo and wild animals. Details of the supplier of the safety data sheet Registered company name Virbac (Australia) Pty Limited Address 361 Horsley Road Milperra NSW 2214 Australia Telephone 1800 242 100 Fax +61 2 9772 9773 Website au.virbac.com Email [email protected] Emergency telephone number Association / Organisation Poisons Information Centre Emergency telephone 13 11 26 numbers Other emergency telephone Not Available numbers SECTION 2 Hazards identification Classification of the substance or mixture NON-HAZARDOUS CHEMICAL. NON-DANGEROUS GOODS. According to the WHS Regulations and the ADG Code. ChemWatch Hazard Ratings Min Max Flammability 1 Toxicity 1 0 = Minimum Body Contact 1 1 = Low 2 = Moderate Reactivity 1 3 = High Chronic 0 4 = Extreme Poisons Schedule S4 Classification [1] Not Applicable Label elements Hazard pictogram(s) Not Applicable Signal word Not Applicable Hazard statement(s) Not Applicable Precautionary statement(s) Prevention Not Applicable Precautionary statement(s) Response Not Applicable Precautionary statement(s) Storage Page 1 continued.. -
Quest Diagnostics Prescription Drug Monitoring Reference Guide
Clinical Drug Monitoring Reference Guide Clinical Drug Monitoring Test List with Test Codes Drug Class P P,D,M P,D D,M D Drug Class P P,D,M P,D D,M D Drug Class P P,D,M P,D D,M D Alcohol Metabolites 90079 16910 92142 16217 Cocaine Metabolite 92225 70248 16888 90082 16916 Naltrexone 93753 Amphetamines 92222 70245 16885 70209 16913 Eszopiclone 91251 Opiates 92230 18991 16891 70237* 16298* Amphetamines Fentanyl 36278 36279 36280 18996 16900 Oxycodone 92231 18992 16892 70238 16920 91590 91589 92484 92483 with Reflex d/l Isomers Gabapentin 70205 16904 Phencyclidine 92232 18993 16893 90083 16921 Antidepressants (urine) 94032 Heroin Metabolite 92226 90081 16911 90333 90329 Pregabalin 70208 16908 Antidepressants (serum) 94031 Marijuana Metabolite 92227 18989 16889 70233 16917 Propoxyphene 92233 18995 16894 70239 16922 Antipsychotics (urine) 94528 MDMA/MDA 92228 90078 16909 90334 90331 Synthetic Cannabinoids 93027 Antipsychotics (serum) 94529 Meperidine 70206 16905 Synthetic Stimulants 90322 Barbiturates 92223 70246 16886 70230 16912 Methadone Metabolite 92229 18990 16890 70234 16918 Tapentadol 90244 90243 Benzodiazepines 92224 70247 16887 70231 16914 Methamphetamine Tramadol 70207 16906 90319 Buprenorphine 16207 70249 16901 18998 16213 d/l Isomers Tricyclic Antidepressants 70204 16903 Buprenorphine 93093 93094 Methylphenidate 90247 90246 with Naloxone Zolpidem 91258 Mitragynine 39241 39240 Carisoprodol 18999 16902 *Includes oxycodone drug class Test Profiles Profile Name Base Profile Profile 1 Profile 2 Profile 3 Profile 4 Profile 5 Profile 6 -
Patient Risks & Preparation for a Successful Sedation Or Anesthetic Event
Patient risks & Sleep preparation for a successful well… sedation or anesthetic event Odette O, DVM, DACVAA ▪ Sedation versus general anesthetic: what are the considerations? ▪ What are the risks (literally) of sedation &/or anesthesia? ▪ Optimize patient preparation prior to sedation/anesthesia whenever possible! ▪ Be prepared: Who? What? Where? When? Why? ▪ Troubleshooting a rough recovery… ▪ ↑ risk of mortality seen with increasing ASA status ▪ Importance of patient evaluation and stabilization PRIOR to commencement of procedure ▪ Identify risk factors and monitor carefully ▪ Largest proportion of deaths in post-procedure period ▪ Continued patient monitoring & support vital • Diagnostic Imaging • Radiographs, CT, U/S • Biopsies • Small wound repair • Bandaging • Convenience • Faster recovery times • Reversible options • ↓ $ • ↑ margin of safety ▪ Reversible unconsciousness ▪ Amnesia ▪ Analgesia ▪ Muscle relaxation ▪ Perform a procedure ▪ w/o suffering ▪ Safety ▪ Patient ▪ Veterinary Care Provider(s) ▪ Multi-modal approach ▪ DO NOT “mask down” (canine/feline) patients! ▪ Patient & occupational safety concerns ▪ MAC (minimum alveolar concentration) = amount of inhalant needed for 50% of patients non- responsive to supramaximal stimulus ▪ Isoflurane: ≈ 1.3% canine, ≈1.6% feline ▪ Sevoflurane: ≈ 2.3% canine, ≈ 3% feline ▪ allows estimate of amount inhalant required ▪ factors: procedure, patient pre-med response, inhalant ▪ Minimal calculations needed ▪ Inhalant effective in every species we encounter ▪ Predictable effects on most patients, -
Properties and Units in Clinical Pharmacology and Toxicology
Pure Appl. Chem., Vol. 72, No. 3, pp. 479–552, 2000. © 2000 IUPAC INTERNATIONAL FEDERATION OF CLINICAL CHEMISTRY AND LABORATORY MEDICINE SCIENTIFIC DIVISION COMMITTEE ON NOMENCLATURE, PROPERTIES, AND UNITS (C-NPU)# and INTERNATIONAL UNION OF PURE AND APPLIED CHEMISTRY CHEMISTRY AND HUMAN HEALTH DIVISION CLINICAL CHEMISTRY SECTION COMMISSION ON NOMENCLATURE, PROPERTIES, AND UNITS (C-NPU)§ PROPERTIES AND UNITS IN THE CLINICAL LABORATORY SCIENCES PART XII. PROPERTIES AND UNITS IN CLINICAL PHARMACOLOGY AND TOXICOLOGY (Technical Report) (IFCC–IUPAC 1999) Prepared for publication by HENRIK OLESEN1, DAVID COWAN2, RAFAEL DE LA TORRE3 , IVAN BRUUNSHUUS1, MORTEN ROHDE1, and DESMOND KENNY4 1Office of Laboratory Informatics, Copenhagen University Hospital (Rigshospitalet), Copenhagen, Denmark; 2Drug Control Centre, London University, King’s College, London, UK; 3IMIM, Dr. Aiguader 80, Barcelona, Spain; 4Dept. of Clinical Biochemistry, Our Lady’s Hospital for Sick Children, Crumlin, Dublin 12, Ireland #§The combined Memberships of the Committee and the Commission (C-NPU) during the preparation of this report (1994–1996) were as follows: Chairman: H. Olesen (Denmark, 1989–1995); D. Kenny (Ireland, 1996); Members: X. Fuentes-Arderiu (Spain, 1991–1997); J. G. Hill (Canada, 1987–1997); D. Kenny (Ireland, 1994–1997); H. Olesen (Denmark, 1985–1995); P. L. Storring (UK, 1989–1995); P. Soares de Araujo (Brazil, 1994–1997); R. Dybkær (Denmark, 1996–1997); C. McDonald (USA, 1996–1997). Please forward comments to: H. Olesen, Office of Laboratory Informatics 76-6-1, Copenhagen University Hospital (Rigshospitalet), 9 Blegdamsvej, DK-2100 Copenhagen, Denmark. E-mail: [email protected] Republication or reproduction of this report or its storage and/or dissemination by electronic means is permitted without the need for formal IUPAC permission on condition that an acknowledgment, with full reference to the source, along with use of the copyright symbol ©, the name IUPAC, and the year of publication, are prominently visible. -
Central Valley Toxicology Drug List
Chloroform ~F~ Lithium ~A~ Chlorpheniramine Loratadine Famotidine Acebutolol Chlorpromazine Lorazepam Fenoprofen Acetaminophen Cimetidine Loxapine Fentanyl Acetone Citalopram LSD (Lysergide) Fexofenadine 6-mono- Clomipramine acetylmorphine Flecainide ~M~ Clonazepam a-Hydroxyalprazolam Fluconazole Maprotiline Clonidine a-Hydroxytriazolam Flunitrazepam MDA Clorazepate Albuterol Fluoxetine MDMA Clozapine Alprazolam Fluphenazine Medazepam Cocaethylene Amantadine Flurazepam Meperidine Cocaine 7-Aminoflunitrazepam Fluvoxamine Mephobarbital Codeine Amiodarone Fosinopril Meprobamate Conine Amitriptyline Furosemide Mesoridazine Cotinine Amlodipine Methadone Cyanide ~G~ Amobarbital Methanol Cyclobenzaprine Gabapentin Amoxapine d-Methamphetamine Cyclosporine GHB d-Amphetamine l-Methamphetamine Glutethamide l-Amphetamine ~D~ Methapyrilene Guaifenesin Aprobarbital Demoxepam Methaqualone Atenolol Desalkylfurazepam ~H~ Methocarbamol Atropine Desipramine Halazepam Methylphenidate ~B~ Desmethyldoxepin Haloperidol Methyprylon Dextromethoraphan Heroin Metoclopramide Baclofen Diazepam Hexobarbital Metoprolol Barbital Digoxin Hydrocodone Mexiletine Benzoylecgonine Dihydrocodein Hydromorphone Midazolam Benzphetamine Dihydrokevain Hydroxychloroquine Mirtazapine Benztropine Diltiazem Hydroxyzine Morphine (Total/Free) Brodificoum Dimenhydrinate Bromazepam ~N~ Diphenhydramine ~I~ Bupivacaine Nafcillin Disopyramide Ibuprofen Buprenorphine Naloxone Doxapram Imipramine Bupropion Naltrexone Doxazosin Indomethacin Buspirone NAPA Doxepin Isoniazid Butabarbital Naproxen -
Download Product Insert (PDF)
PRODUCT INFORMATION Tiletamine (hydrochloride) Item No. 19794 CAS Registry No.: 14176-50-2 Formal Name: 2-(ethylamino)-2-(2- thienyl)-cyclohexanone, S monohydrochloride Synonyms: CI-634, CL-399, CN 54521-2, HN NSC 167740 O MF: C12H17NOS • HCl FW: 259.8 Purity: ≥98% • HCl UV/Vis.: λmax: 236 nm Supplied as: A crystalline solid Storage: -20°C Stability: As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly Description Tiletamine (hydrochloride) (Item No. 19794) is an analytical reference standard that is structurally classified as an arylcyclohexylamine. It is a non-competitive NMDA receptor antagonist used in veterinary medicine for its anesthetic and sedative properties, which are comparable to ketamine (Item No. 11630).1,2 Abuse of this compound has been documented.2 It is intended for forensic and research purposes only. References 1. Klockgether, T., Turski, L., Schwarz, M., et al. Paradoxical convulsant action of a novel non-competitive N-methyl-D-aspartate (NMDA) antagonist, tiletamine. Brain Res. 461(2), 343-348 (1988). 2. Quail, M. T., Weimersheimer, P., Woolf, A. D., et al. Abuse of telazol: An animal tranquilizer. J. Toxicol. Clin. Toxicol. 39(4), 399-402 (2001). WARNING CAYMAN CHEMICAL THIS PRODUCT IS FOR RESEARCH ONLY - NOT FOR HUMAN OR VETERINARY DIAGNOSTIC OR THERAPEUTIC USE. 1180 EAST ELLSWORTH RD SAFETY DATA ANN ARBOR, MI 48108 · USA This material should be considered hazardous until further information becomes available. Do not ingest, inhale, get in eyes, on skin, or on clothing. Wash thoroughly after handling. Before use, the user must review the complete Safety Data Sheet, which has been sent via email to your institution. -
The Role of the N-Methyl-D-Aspartate Receptors in Social Behavior in Rodents
International Journal of Molecular Sciences Review The Role of the N-Methyl-D-Aspartate Receptors in Social Behavior in Rodents Iulia Zoicas * and Johannes Kornhuber Department of Psychiatry and Psychotherapy, University Hospital, Friedrich-Alexander-University Erlangen-Nuremberg, 91054 Erlangen, Germany; [email protected] * Correspondence: [email protected]; Tel.: +49-9131-85-46005; Fax: +49-9131-85-36381 Received: 8 October 2019; Accepted: 5 November 2019; Published: 9 November 2019 Abstract: The appropriate display of social behaviors is essential for the well-being, reproductive success and survival of an individual. Deficits in social behavior are associated with impaired N-methyl-D-aspartate (NMDA) receptor-mediated neurotransmission. In this review, we describe recent studies using genetically modified mice and pharmacological approaches which link the impaired functioning of the NMDA receptors, especially of the receptor subunits GluN1, GluN2A and GluN2B, to abnormal social behavior. This abnormal social behavior is expressed as impaired social interaction and communication, deficits in social memory, deficits in sexual and maternal behavior, as well as abnormal or heightened aggression. We also describe the positive effects of pharmacological stimulation of the NMDA receptors on these social deficits. Indeed, pharmacological stimulation of the glycine-binding site either by direct stimulation or by elevating the synaptic glycine levels represents a promising strategy for the normalization of genetically-induced, pharmacologically-induced or innate deficits in social behavior. We emphasize on the importance of future studies investigating the role of subunit-selective NMDA receptor ligands on different types of social behavior to provide a better understanding of the underlying mechanisms, which might support the development of selective tools for the optimized treatment of disorders associated with social deficits. -
Highlights of This Issue
THURSDAY, OCTOBER 4, 1973 WASHINGTON, D.C. HIGHLIGHTS OF THIS ISSUE This listing does not affect the legal status of any document published in this issue. Detailed table of contents appears inside. ECONOMIC STABILIZATION— CLC Phase IV pay and price regulations for certain reg istered, practical, and trained nurses (2 documents); effective 10—1—73....................... ........................ 27528, 27529 CLC allows Phase IV price increases for rubber tire and tube products; effective 10—8—73............................. ....... 27528 October 4, 1973— -Pages 27501-27574 METHAQUALONE— Justice Department classifies as Schedule II controlled substance; effective 10—4—73 27516 ARTISTS' PAINTS AND SUPPLIES— Consumer Product Safety Commission exempts from lead content restric tions; effective 12—3—73...-......... ........................................ 27514 DEFENSE CONTRACTS— Cost Amounting Standards Board extends disclosure statement filing requirements; effective 4— 1—74............................. ....................................... 27507 PUBLIC ASSISTANCE— HEW proposal on determin ing paternity of children receiving aid; comments by 1 1 -5 -7 3 ............................................ -. ............ : ........ 27530 SUGAR— USDA declares and reprorates 1973 quota deficits for Hawaii and Peru................... .................... ........................ 27509 USDA requires no proportionate shares for 1974 sugarbeet crop..--....................... ..............."...................... — 27510 PEANUTS— USDA proposes 1974 -
Anesthetic and Physiologic Effects of Tiletamine, Zolazepam, Ketamine, and Xylazine Combination (TKX) in Feral Cats Undergoing Surgical Sterilization
Journal of Feline Medicine and Surgery (2004) 6, 297e303 www.elsevier.com/locate/jfms Anesthetic and physiologic effects of tiletamine, zolazepam, ketamine, and xylazine combination (TKX) in feral cats undergoing surgical sterilization Alexis M. Cistolaa, Francis J. Golderb, Lisa A. Centonzea, ) Lindsay W. McKaya, Julie K. Levya, aDepartment of Small Animal Clinical Sciences, PO Box 100126, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA bDepartment of Comparative Bioscience, College of Veterinary Medicine, University of Wisconsin, Madison, WI 53706, USA Revised 23 November 2003; accepted 26 November 2003 Summary Tiletamine (12.5 mg), zolazepam (12.5 mg), ketamine (20 mg), and xylazine (5mg)(TKX;0.25ml,IM)combinationwasevaluatedasananestheticin22maleand67 female adult feral cats undergoing sterilization at high-volume sterilization clinics. Cats were not intubated and breathed room air. Oxygen saturation (SpO2), mean blood pres- sure (MBP), heart rate (HR), respiration rate (RR), and core body temperature were re- corded. Yohimbine (0.25 ml, 0.5 mg, IV) was administered at the completion of surgery. TKXproducedrapidonsetoflateralrecumbency(4G1 min) and surgical anesthesia of sufficient duration to complete surgical procedures in 92% of cats. SpO2 measured via a lingual pulse oximeter probe averaged 92G3% in male cats and 90G4% in females. SpO2 fell below 90% at least once in most cats. MBPmeasuredbyoscillometryaveraged 136G30 mm Hg in males and 113G29 mm Hg in females. MBP increased at the onset of surgical stimulation suggesting incomplete anti-nociceptive properties. HR averaged 156G19bpm,andRRaveraged18G8 bpm. Neither parameter varied between males and females or over time. Body temperature decreased significantly over time, declining to 38.0G0.8 (C at the time of reversal in males and 36.6G0.8 (Catthetimeofreversal in females. -
Drug Detection Time Window Chart
Chesapeake Toxicology Resources Drug Detection Windows Updated as of December, 15th 2014 The length of time that the presence of drugs of abuse in the body can be detected is an important factor in drug screening. The chart below outlines approximate duration times. When interpreting the duration for the presence of drugs of abuse in the body, you must take into consideration variables including the body's metabolism, the subject's physical condition, overall body fluid balance, state of hydration and frequency of usage. Amphetamines Drug Name Metabolite Detection Window Prescription Names Amphetamine 3-5 Days Adderall, Adderall XR, Dexedrine, Spansule, DextroStat MDA 2-5 Days Tenamfetamine MDMA MDA 1-3 Days Adam, Ecstacy Methamphetamine Amphetamine 3-5 Days Desoxyn, Desoxyn Gradument Anti-epileptics Drug Name Metabolite Detection Window Prescription Names Gabapentin 1-5 Days Neurontin, Nupentin, Fanatrex, Gabarone, Gralise Pregablin 1-4 Days Lyrica CHESAPEAKE TOXICOLOGY RESOURCES- DRUG DETECTION TIMETABLE !1 Barbiturates Drug Name Metabolite Detection Window Prescription Names Amobarbital 2-10 Days Amytal, Amylobarbiton, Tuinal Butalbital 4-6 Days Axocet, Axotal, Bucet, Bupap, Butex Forte, Cephadyn, Dolgic, Esgic, Esgic-Plus, Fioricet, Fiorinal, Fiormor, Fiortal, Fortabs, Laniroif, Margesic, Marten-Tab, Medigesic, Phrenilin, Phrenilin Forte, Repan, Sedapap, Tencon, Triad Pentobarbital 2-10 Days Euthasol, Nembutal , Nembutal Sodium, Pentasol Phenobarbital Up to 16 days Antrocol, Barbidonna, Barbita, Bellacane, Bellatal, Bellergal-S, Chardonna-2, -
21 CFR Ch. II (4–1–10 Edition) § 1308.12
§ 1308.12 21 CFR Ch. II (4–1–10 Edition) Some trade and other names: N,N- whenever the existence of such salts, Diethyltryptamine; DET isomers, and salts of isomers is possible (18) Dimethyltryptamine ................................................. 7435 Some trade or other names: DMT within the specific chemical designa- (19) 5-methoxy-N,N-diisopropyltryptamine (other tion: name: 5-MeO-DIPT) ................................................... 7439 (1) gamma-hydroxybutyric acid (some other names in- (20) Ibogaine .................................................................. 7260 clude GHB; gamma-hydroxybutyrate; 4- Some trade and other names: 7-Ethyl- hydroxybutyrate; 4-hydroxybutanoic acid; sodium 6,6b,7,8,9,10,12,13-octahydro-2-methoxy-6,9- oxybate; sodium oxybutyrate) .................................... 2010 methano-5H-pyrido [1′, 2′:1,2] azepino [5,4-b] (2) Mecloqualone ........................................................... 2572 indole; Tabernanthe iboga (3) Methaqualone ........................................................... 2565 (21) Lysergic acid diethylamide ..................................... 7315 (22) Marihuana .............................................................. 7360 (f) Stimulants. Unless specifically ex- (23) Mescaline ............................................................... 7381 cepted or unless listed in another (24) Parahexyl—7374; some trade or other names: 3- schedule, any material, compound, Hexyl-1-hydroxy-7,8,9,10-tetrahydro-6,6,9-trimethyl- 6H-dibenzo[b,d]pyran; Synhexyl. mixture, -
DOCUMENT RESUME ED 300 697 CG 021 192 AUTHOR Gougelet, Robert M.; Nelson, E. Don TITLE Alcohol and Other Chemicals. Adolescent A
DOCUMENT RESUME ED 300 697 CG 021 192 AUTHOR Gougelet, Robert M.; Nelson, E. Don TITLE Alcohol and Other Chemicals. Adolescent Alcoholism: Recognizing, Intervening, and Treating Series No. 6. INSTITUTION Ohio State Univ., Columbus. Dept. of Family Medicine. SPONS AGENCY Health Resources and Services Administration (DHHS/PHS), Rockville, MD. Bureau of Health Professions. PUB DATE 87 CONTRACT 240-83-0094 NOTE 30p.; For other guides in this series, see CG 021 187-193. AVAILABLE FROMDepartment of Family Medicine, The Ohio State University, Columbus, OH 43210 ($5.00 each, set of seven, $25.00; audiocassette of series, $15.00; set of four videotapes keyed to guides, $165.00 half-inch tape, $225.00 three-quarter inch tape; all orders prepaid). PUB TYPE Guides - Classroom Use - Materials (For Learner) (051) -- Reports - General (140) EDRS PRICE MF01 Plus Plstage. PC Not Available from EDRS. DESCRIPTORS *Adolescents; *Alcoholism; *Clinical Diagnosis; *Drug Use; *Family Problems; Physician Patient Relationship; *Physicians; Substance Abuse; Units of Study ABSTRACT This document is one of seven publications contained in a series of materials for physicians on recognizing, intervening with, and treating adolescent alcoholism. The materials in this unit of study are designed to help the physician know the different classes of drugs, recognize common presenting symptoms of drug overdose, and place use and abuse in context. To do this, drug characteristics and pathophysiological and psychological effects of drugs are examined as they relate to administration,