Over-The-Counter Medications for Pets
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Appendix a Common Abbreviations Used in Medication
UNIVERSITY OF AMSTERDAM MASTERS THESIS Impact of Medication Grouping on Fall Risk Prediction in Elders: A Retrospective Analysis of MIMIC-III Critical Care Database Student: SRP Mentor: Noman Dormosh Dr. Martijn C. Schut Student No. 11412682 – SRP Tutor: Prof. dr. Ameen Abu-Hanna SRP Address: Amsterdam University Medical Center - Location AMC Department Medical Informatics Meibergdreef 9, 1105 AZ Amsterdam Practice teaching period: November 2018 - June 2019 A thesis submitted in fulfillment of the requirements for the degree of Master of Medical Informatics iii Abstract Background: Falls are the leading cause of injury in elderly patients. Risk factors for falls in- cluding among others history of falls, old age, and female gender. Research studies have also linked certain medications with an increased risk of fall in what is called fall-risk-increasing drugs (FRIDs), such as psychotropics and cardiovascular drugs. However, there is a lack of consistency in the definitions of FRIDs between the studies and many studies did not use any systematic classification for medications. Objective: The aim of this study was to investigate the effect of grouping medications at different levels of granularity of a medication classification system on the performance of fall risk prediction models. Methods: This is a retrospective analysis of the MIMIC-III cohort database. We created seven prediction models including demographic, comorbidity and medication variables. Medica- tions were grouped using the anatomical therapeutic chemical classification system (ATC) starting from the most specific scope of medications and moving up to the more generic groups: one model used individual medications (ATC level 5), four models used medication grouping at levels one, two, three and four of the ATC and one model did not include med- ications. -
Activated Charcoal for Acute Poisoning: One Toxicologist's Journey
J. Med. Toxicol. (2010) 6:190–198 DOI 10.1007/s13181-010-0046-1 REVIEW ARTICLE Activated Charcoal for Acute Poisoning: One Toxicologist’s Journey Kent R. Olson Published online: 20 May 2010 # The Author(s) 2010. This article is published with open access at Springerlink.com Keywords Activated charcoal . Gastrointestinal As summarized by Matthew [13], Harstad and Danish decontamination . Poisoning . Drug overdose colleagues reported in 1942 that relatively little phenobar- bital was recovered by lavage even shortly after overdose [14] and this, along with their finding of particles of When I began studying clinical toxicology in 1981, the issue charcoal in the lungs of patients who died, led them to call of gastrointestinal decontamination after acute ingestion for the abandonment of gastric lavage for poisoning.) “ ” seemed pretty well settled: universal antidote, apomor- In recent years, my colleagues and I have continued to – phine and salt wateremesiswerenolongerused[1, 2]; and I debate the value of various methods of gastric decontam- was taught that barring a specific contraindication, the awake ination and the role and risks of activated charcoal, and it is patient was given syrup of ipecac to induce emesis, and the clear to me that the issue remains muddy. Some have taken drowsy or uncooperative patient was lavaged [3]. After a firm stand that no treatment should be recommended that is gastric emptying, everyone received activated charcoal not supported by evidence from a randomized controlled trial (AC). The only controversy seemed to be over whether one (RCT). Position statements published jointly by the Amer- should add a cathartic to speed gastrointestinal transit [4]. -
Treatment of Self-Poisoned Adults G
Archives of Emergency Medicine, 1985, 2, 203-208 Ipecacuanha induced emesis in the treatment of self-poisoned adults G. GORDON Accident and Emergency Department, Manor Hospital, Nuneaton, Warwickshire, England SUMMARY One hundred consecutive adult patients presenting to an Accident and Emergency Department following intentional self-poisoning were given 50 to 80 ml Paediatric Ipecacuanha Emetic Mixture BP as an emetic, together with two or three glasses of strong orange juice. A satisfactory emetic result was obtained in 99 patients. No toxic effects were noted in these patients, or in the one patient in whom emesis did not occur, and who subsequently refused gastric lavage. The potential toxicity of Ipecacuanha Syrup itself is discussed, and attention drawn to the lower Emetine content of Paediatric Ipecacuanha Emetic Mixture (BP), rather than that of the formulations used in previously published reports. The use of Paediatric Ipecacuanha Emetic Mixture B.P. in adults is effective and safe in this dosage. INTRODUCTION The methods available for retrieval of poisoning agents from the stomach are gastric lavage and emesis. In the United Kingdom at the present time, gastric lavage is the method most commonly used in the treatment of adults. It is an unpleasant and time consuming procedure for both patient and staff, and it is not without risk (Matthew et al., 1966), even in the hands of the experienced nursing staff who usually carry it out. Doubt still remains about its effectiveness (Goulding & Volans, 1977), and the basis for its use rests more on the occasional recovery of large quantities of drug, rather than verification of its routine efficiency by studies in man (Melman & Morelli, 1978). -
)&F1y3x PHARMACEUTICAL APPENDIX to THE
)&f1y3X PHARMACEUTICAL APPENDIX TO THE HARMONIZED TARIFF SCHEDULE )&f1y3X PHARMACEUTICAL APPENDIX TO THE TARIFF SCHEDULE 3 Table 1. This table enumerates products described by International Non-proprietary Names (INN) which shall be entered free of duty under general note 13 to the tariff schedule. The Chemical Abstracts Service (CAS) registry numbers also set forth in this table are included to assist in the identification of the products concerned. For purposes of the tariff schedule, any references to a product enumerated in this table includes such product by whatever name known. Product CAS No. Product CAS No. ABAMECTIN 65195-55-3 ACTODIGIN 36983-69-4 ABANOQUIL 90402-40-7 ADAFENOXATE 82168-26-1 ABCIXIMAB 143653-53-6 ADAMEXINE 54785-02-3 ABECARNIL 111841-85-1 ADAPALENE 106685-40-9 ABITESARTAN 137882-98-5 ADAPROLOL 101479-70-3 ABLUKAST 96566-25-5 ADATANSERIN 127266-56-2 ABUNIDAZOLE 91017-58-2 ADEFOVIR 106941-25-7 ACADESINE 2627-69-2 ADELMIDROL 1675-66-7 ACAMPROSATE 77337-76-9 ADEMETIONINE 17176-17-9 ACAPRAZINE 55485-20-6 ADENOSINE PHOSPHATE 61-19-8 ACARBOSE 56180-94-0 ADIBENDAN 100510-33-6 ACEBROCHOL 514-50-1 ADICILLIN 525-94-0 ACEBURIC ACID 26976-72-7 ADIMOLOL 78459-19-5 ACEBUTOLOL 37517-30-9 ADINAZOLAM 37115-32-5 ACECAINIDE 32795-44-1 ADIPHENINE 64-95-9 ACECARBROMAL 77-66-7 ADIPIODONE 606-17-7 ACECLIDINE 827-61-2 ADITEREN 56066-19-4 ACECLOFENAC 89796-99-6 ADITOPRIM 56066-63-8 ACEDAPSONE 77-46-3 ADOSOPINE 88124-26-9 ACEDIASULFONE SODIUM 127-60-6 ADOZELESIN 110314-48-2 ACEDOBEN 556-08-1 ADRAFINIL 63547-13-7 ACEFLURANOL 80595-73-9 ADRENALONE -
Injectable Anesthesia in South American Camelids
INJECTABLE ANESTHESIA IN SOUTH AMERICAN CAMELIDS Thomas Riebold DVM, Diplomate ACVAA Veterinary Teaching Hospital College of Veterinary Medicine Oregon State University Corvallis, Oregon 97331 INTRODUCTION Interest in llamas, and more recently in alpacas, as pets and as breeding and pack animals has led to increased demand for veterinary services for them. While they have some unique species characteristics regarding anesthesia, many of the principles and techniques used in food animal and equine anesthesia also apply to South American camelids. Except for differences in size, anesthetic management of alpacas and llamas is similar. Much like there are species differences between cattle, sheep, and goats in their response to xylazine, it does appear that alpacas require higher doses of sedatives, approximately 10-20%, to obtain the same response that lower doses of sedatives would obtain in llamas. PREANESTHETIC CONSIDERATIONS Consideration for preanesthetic preparation includes fasting, assessment of hematologic and blood chemistry values, venous catheterization, and estimation of bodyweight. The camelid has a stomach divided into three compartments. Therefore, potential complications similar to those of domestic ruminants, regurgitation and aspiration pneumonia, exist during anesthesia. Abdominal tympany as it occurs in anesthetized domestic ruminants does not appear to occur in anesthetized camelids. It is recommended that the animals be fasted 12-18 hours and deprived of water for 8-12 hours. In nonelective cases, this is often not possible and precautions should be taken to avoid aspiration of gastric fluid and ingesta. Fasting neonatal camelids is not advisable because hypoglycemia may result. As in other species, hematologic and blood chemistry values are determined before anesthesia. -
“Opioid” Definition Drug Inclusion and Exclusion List
WSHA WSMA Opioid Prescribing Report Medication Inclusion/Exclusion list For purposes of developing WSHA WSMA Opioid Prescribing Report metrics, the following medications tracked in the Prescription Monitoring Program database were included and counted as “opioid prescriptions”: Drug Name ACETAMINOPHEN-CODEINE ASCOMP WITH CODEINE BELLADONNA-OPIUM BUTALB-ACETAMINOPH-CAFF-CODEIN BUTALB-CAFF-ACETAMINOPH-CODEIN BUTALBITAL COMPOUND-CODEINE BUTORPHANOL TARTRATE CARISOPRODOL-ASPIRIN-CODEINE CHERATUSSIN AC CHERATUSSIN DAC CODEINE SULFATE CODEINE-GUAIFENESIN DEMEROL DILAUDID DOLOPHINE HCL DURAMORPH ENDOCET FENTANYL CITRATE FENTORA FIORICET WITH CODEINE FIORINAL WITH CODEINE #3 GUAIATUSSIN AC GUAIFENESIN AC GUAIFENESIN DAC GUAIFENESIN W/CODEINE GUAIFENESIN-CODEINE HYDROCODONE BITARTRATE HYDROCODONE BT-HOMATROPINE MBR HYDROCODONE-ACETAMINOPHEN HYDROCODONE-CHLORPHENIRAMNE ER HYDROCODONE-HOMATROPINE MBR HYDROCODONE-IBUPROFEN HYDROMET HYDROMORPHONE HCL INFUMORPH IOPHEN-C NR LAZANDA LEVORPHANOL TARTRATE LORTAB MEPERIDINE HCL MORPHINE SULFATE NORCO NUCYNTA OPANA OPIUM TINCTURE OXAYDO OXYCODONE HCL OXYCODONE HCL-ASPIRIN OXYCODONE HCL-IBUPROFEN OXYCODONE HYDROCHLORIDE OXYCODONE-ACETAMINOPHEN OXYMORPHONE HCL PENTAZOCINE-NALOXONE HCL PERCOCET PRIMLEV PROMETHAZINE VC-CODEINE PROMETHAZINE-CODEINE PROMETHAZINE-PHENYLEPH-CODEINE ROXICODONE SUBSYS SUFENTANIL CITRATE TRAMADOL HCL TRAMADOL HCL-ACETAMINOPHEN TUSSIGON TUSSIONEX TYLENOL-CODEINE NO.3 TYLENOL-CODEINE NO.4 ULTRACET ULTRAM VICODIN VICODIN ES VICODIN HP VIRTUSSIN AC Other medications, used primarily to -
Poison/Drug Emergencies 1. Which Alcohol Is Used As an Antidote For
Student ID: 22195894 Exam: 084084RR - Poison/Drug Emergencies When you have completed your exam and reviewed your answers, click Submit Exam. Answers will not be recorded until you hit Submit Exam. If you need to exit before completing the exam, click Cancel Exam. Questions 1 to 20: Select the best answer to each question. Note that a question and its answers may be split across a page break, so be sure that you have seen the entire question and all the answers before choosing an answer. 1. Which alcohol is used as an antidote for ethylene glycol ingestions? A. Ethanol B. Isopropanol C. Methanol D. Tetradecanol 2. Which of the following statements about syrup of ipecac is not correct? A. Ipecac stimulates the area in the brain responsible for nausea and vomiting. B. Ipecac has a local irritant effect on the stomach. C. Ipecac should be used to induce vomiting in all patients, regardless of age or condition. D. Ipecac contains two active substances, emetine and cephaeline. 3. The odor of wintergreen on a child's breath might indicate ingestion of which chemical? A. Sodium hypochlorite B. Toluene C. Methyl salicylate D. Paradichlorobenzene 4. _______ is used to reverse an opiate (such as morphine or codeine) overdose. A. Flumazenil B. Atropine C. Naloxone D. Deferoxamine 5. Which of the following statements about syrup of ipecac is not correct? A. American poison control centers rarely recommend syrup of ipecac as an intervention. B. The side effects of ipecac ingestion include prolonged vomiting and lethargy. C. Syrup of ipecac has been available for years in pharmacies over-the-counter. -
Use of Antitussives After the Initiation of Angiotensin-Converting Enzyme Inhibitors
저작자표시-비영리-변경금지 2.0 대한민국 이용자는 아래의 조건을 따르는 경우에 한하여 자유롭게 l 이 저작물을 복제, 배포, 전송, 전시, 공연 및 방송할 수 있습니다. 다음과 같은 조건을 따라야 합니다: 저작자표시. 귀하는 원저작자를 표시하여야 합니다. 비영리. 귀하는 이 저작물을 영리 목적으로 이용할 수 없습니다. 변경금지. 귀하는 이 저작물을 개작, 변형 또는 가공할 수 없습니다. l 귀하는, 이 저작물의 재이용이나 배포의 경우, 이 저작물에 적용된 이용허락조건 을 명확하게 나타내어야 합니다. l 저작권자로부터 별도의 허가를 받으면 이러한 조건들은 적용되지 않습니다. 저작권법에 따른 이용자의 권리는 위의 내용에 의하여 영향을 받지 않습니다. 이것은 이용허락규약(Legal Code)을 이해하기 쉽게 요약한 것입니다. Disclaimer 약학 석사학위 논문 안지오텐신 전환 효소 억제제 개시 이후 진해제의 사용 분석 Use of Antitussives After the Initiation of Angiotensin-Converting Enzyme Inhibitors 2017년 8월 서울대학교 대학원 약학과 사회약학전공 권 익 태 안지오텐신 전환 효소 억제제 개시 이후 진해제의 사용 분석 Use of Antitussives After the Initiation of Angiotensin-Converting Enzyme Inhibitors 지도교수 홍 송 희 이 논문을 권익태 석사학위논문으로 제출함 2017년 4월 서울대학교 대학원 약학과 사회약학전공 권 익 태 권익태의 석사학위논문을 인준함 2017년 6월 위 원 장 (인) 부 위 원 장 (인) 위 원 (인) Abstract Use of Antitussives After the Initiation of Angiotensin-Converting Enzyme Inhibitors Ik Tae Kwon Department of Social Pharmacy College of Pharmacy, Seoul National University Background Angiotensin-converting enzyme inhibitors (ACEI) can induce a dry cough, more frequently among Asians. If healthcare professionals fail to detect coughs induced by an ACEI, patients are at risk of getting antitussives inappropriately instead of discontinuing ACEI. The purpose of this study was to examine how the initiation of ACEI affects the likelihood of antitussive uses compared with the initiation of Angiotensin Receptor Blocker (ARB) and to determine the effect of the antitussive use on the duration and adherence of therapy in a Korean population. -
Helicidine, Un Extrait Doses May Be Given
1562 Cough Suppressants Expectorants Mucolytics and Nasal Decongestants UK preparations suggest that these doses be given up to a maxi- ◊ References. Ipecacuanha mum of 4 times daily, although in other countries higher total 1. Pons F, et al. L’effect bronchorelaxant de l’helicidine, un extrait doses may be given. d’Helix pomatia, fait intervenir une liberation de prostaglandine Hlavěnkový kořen; Ipecac; Ipecacuana; Ipécacuanha, racine d’; E2. Pathol Biol (Paris) 1999; 47: 73–80. Respiratory disorders. An FDA review of preparations avail- Ipecacuanha Root; Ipecacuanhae radix; Ipekakuána-gyökér; able over-the-counter concluded that guaifenesin was an effec- Preparations Ipekakuananjuuri (ipecacuanha root); Ipekakuanarot (ipecacuan- tive expectorant.1 The use of expectorants for productive cough Proprietary Preparations (details are given in Part 3) ha root); Ipekakuanu˛ šaknys; Korzeń ipekakuany; Raíz de ipecac- 2 uana. is discussed on p.1547. A small study found that guaifenesin Multi-ingredient: Ger.: Original Schneckensirup†. also appeared to reduce cough reflex sensitivity in patients with Ипекакуана upper respiratory-tract infections, which produce a transient in- CAS — 8012-96-2. crease in sensitivity, although it had no effect on cough reflex in ATC — R05CA04; V03AB01. Indanazoline Hydrochloride (rINNM) ⊗ healthy subjects. The mechanism for this effect was unclear. ATC Vet — QR05CA04; QV03AB01. Guaifenesin has been given to patients with altered nasal muco- Hidrocloruro de indanazolina; Indanazolin Hidroklorür; Indana- 3 Pharmacopoeias. In Eur. (see p.vii), Int., Jpn, and US. ciliary clearance associated with HIV infection. zoline, Chlorhydrate d’; Indanazolini Hydrochloridum. 1. Thomas J. Guaiphenesin—an old drug now found to be effective. Eur., Jpn, and US also include a monograph for Prepared Ipecac- Aust J Pharm 1990; 71: 101–3. -
Assessment Report on Hedera Helix L., Folium Final
24 November 2015 EMA/HMPC/586887/2014 Committee on Herbal Medicinal Products (HMPC) Assessment report on Hedera helix L., folium Final Based on Article 10a of Directive 2001/83/EC as amended (well-established use) Herbal substance(s) (binomial scientific name of Hedera helix L., folium the plant, including plant part) Herbal preparation(s) a) Dry extract (DER 4-8:1), extraction solvent ethanol 24-30% m/m b) Dry extract (DER 6-7:1), extraction solvent ethanol 40% m/m c) Dry extract (DER 3-6:1), extraction solvent ethanol 60% m/m d) Liquid extract (DER 1:1), extraction solvent ethanol 70% V/V e) Soft extract (DER 2.2-2.9:1), extraction solvent ethanol 50% V/V:propylene glycol (98:2) Pharmaceutical form(s) Herbal preparations in liquid or solid dosage forms for oral use. Rapporteur J. Wiesner Assessor M. Peikert Peer-reviewer I. Chinou 30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 Send a question via our website www.ema.europa.eu/contact An agency of the European Union © European Medicines Agency, 2016. Reproduction is authorised provided the source is acknowledged. Table of contents Table of contents ......................................................................................... 2 1. Introduction ............................................................................................ 4 1.1. Description of the herbal substance(s), herbal preparation(s) or combinations thereof .. 4 1.2. Search and assessment methodology ..................................................................... 5 2. Data on medicinal use ............................................................................. 5 2.1. Information about products on the market in EU/EEA the Member States .................... 5 2.2. Information on documented medicinal use and historical data from literature ............. -
Estonian Statistics on Medicines 2016 1/41
Estonian Statistics on Medicines 2016 ATC code ATC group / Active substance (rout of admin.) Quantity sold Unit DDD Unit DDD/1000/ day A ALIMENTARY TRACT AND METABOLISM 167,8985 A01 STOMATOLOGICAL PREPARATIONS 0,0738 A01A STOMATOLOGICAL PREPARATIONS 0,0738 A01AB Antiinfectives and antiseptics for local oral treatment 0,0738 A01AB09 Miconazole (O) 7088 g 0,2 g 0,0738 A01AB12 Hexetidine (O) 1951200 ml A01AB81 Neomycin+ Benzocaine (dental) 30200 pieces A01AB82 Demeclocycline+ Triamcinolone (dental) 680 g A01AC Corticosteroids for local oral treatment A01AC81 Dexamethasone+ Thymol (dental) 3094 ml A01AD Other agents for local oral treatment A01AD80 Lidocaine+ Cetylpyridinium chloride (gingival) 227150 g A01AD81 Lidocaine+ Cetrimide (O) 30900 g A01AD82 Choline salicylate (O) 864720 pieces A01AD83 Lidocaine+ Chamomille extract (O) 370080 g A01AD90 Lidocaine+ Paraformaldehyde (dental) 405 g A02 DRUGS FOR ACID RELATED DISORDERS 47,1312 A02A ANTACIDS 1,0133 Combinations and complexes of aluminium, calcium and A02AD 1,0133 magnesium compounds A02AD81 Aluminium hydroxide+ Magnesium hydroxide (O) 811120 pieces 10 pieces 0,1689 A02AD81 Aluminium hydroxide+ Magnesium hydroxide (O) 3101974 ml 50 ml 0,1292 A02AD83 Calcium carbonate+ Magnesium carbonate (O) 3434232 pieces 10 pieces 0,7152 DRUGS FOR PEPTIC ULCER AND GASTRO- A02B 46,1179 OESOPHAGEAL REFLUX DISEASE (GORD) A02BA H2-receptor antagonists 2,3855 A02BA02 Ranitidine (O) 340327,5 g 0,3 g 2,3624 A02BA02 Ranitidine (P) 3318,25 g 0,3 g 0,0230 A02BC Proton pump inhibitors 43,7324 A02BC01 Omeprazole -
How to Anesthetize Donkeys for Surgical Procedures in the Field
DRUGS AND ANESTHESIA How to Anesthetize Donkeys for Surgical Procedures in the Field Lori A. Bidwell, DVM, Diplomate ACVA Author’s address: Ross University School of Veterinary Medicine, PO Box 334, St. Kitts, West Indies; e-mail: [email protected]. © 2010 AAEP. 1. Introduction ing a local block where a catheter will be placed and Donkeys are an important part of the work force in making a small skin incision with a surgical blade much of the world. Practitioners working with before placing an intravenous catheter is recom- donkeys in the United States and those participat- mended. Intubation is more difficult because of ing in equitarian initiatives abroad should under- caudal angulation of the larynx, a pharyngeal diver- stand the difference between donkeys and horses in ticulum, excess pharyngeal mucosa, and long paired relation to anesthesia. Although it is tempting to laryngeal saccules. Additionally, nasal intubation 1 treat a donkey like a horse, there are important is complicated by narrow nasal passages. Drug differences in relation to handling and drug doses. metabolism is elevated in donkeys compared with Additionally, it is important to understand alterna- horses, resulting in the use of higher doses and more 2–6 tive anesthetic protocols because a practitioner may frequent dosing intervals. The only known ex- be limited to minimal or alternative drugs when ception to this is the administration of guaifenesin, working in a developing country. which seems to require lower dosing because respi- ratory arrest is easy to achieve when using doses 7 2. Behavior and Physiology appropriate for a horse. A tame donkey can be easy to handle but a feral or minimally handled donkey can be frustrating.