PROPRANOLOL Class: Antianginal Agent;Antiarrhythmic Agent, Class II
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
Drug Class Review Antianginal Agents
Drug Class Review Antianginal Agents 24:12.08 Nitrates and Nitrites 24:04.92 Cardiac Drugs, Miscellaneous Amyl Nitrite Isosorbide Dinitrate (IsoDitrate ER®, others) Isosorbide Mononitrate (Imdur®) Nitroglycerin (Minitran®, Nitrostat®, others) Ranolazine (Ranexa®) Final Report May 2015 Review prepared by: Melissa Archer, PharmD, Clinical Pharmacist Carin Steinvoort, PharmD, Clinical Pharmacist Gary Oderda, PharmD, MPH, Professor University of Utah College of Pharmacy Copyright © 2015 by University of Utah College of Pharmacy Salt Lake City, Utah. All rights reserved. Table of Contents Executive Summary ......................................................................................................................... 3 Introduction .................................................................................................................................... 4 Table 1. Antianginal Therapies .............................................................................................. 4 Table 2. Summary of Agents .................................................................................................. 5 Disease Overview ........................................................................................................................ 8 Table 3. Summary of Current Clinical Practice Guidelines .................................................... 9 Pharmacology ............................................................................................................................... 10 Table 4. Pharmacokinetic Properties -
IHS National Pharmacy & Therapeutics Committee National
IHS National Pharmacy & Therapeutics Committee National Core Formulary; Last Updated: 09/23/2021 **Note: Medications in GREY indicate removed items.** Generic Medication Name Pharmacological Category (up-to-date) Formulary Brief (if Notes / Similar NCF Active? available) Miscellaneous Medications Acetaminophen Analgesic, Miscellaneous Yes Albuterol nebulized solution Beta2 Agonist Yes Albuterol, metered dose inhaler Beta2 Agonist NPTC Meeting Update *Any product* Yes (MDI) (Nov 2017) Alendronate Bisphosphonate Derivative Osteoporosis (2016) Yes Allopurinol Antigout Agent; Xanthine Oxidase Inhibitor Gout (2016) Yes Alogliptin Antidiabetic Agent, Dipeptidyl Peptidase 4 (DPP-4) Inhibitor DPP-IV Inhibitors (2019) Yes Anastrozole Antineoplastic Agent, Aromatase Inhibitor Yes Aspirin Antiplatelet Agent; Nonsteroidal Anti-Inflammatory Drug; Salicylate Yes Azithromycin Antibiotic, Macrolide STIs - PART 1 (2021) Yes Calcium Electrolyte supplement *Any formulation* Yes Carbidopa-Levodopa (immediate Anti-Parkinson Agent; Decarboxylase Inhibitor-Dopamine Precursor Parkinson's Disease Yes release) (2019) Clindamycin, topical ===REMOVED from NCF=== (See Benzoyl Peroxide AND Removed January No Clindamycin, topical combination) 2020 Corticosteroid, intranasal Intranasal Corticosteroid *Any product* Yes Cyanocobalamin (Vitamin B12), Vitamin, Water Soluble Hematologic Supplements Yes oral (2016) Printed on 09/25/2021 Page 1 of 18 National Core Formulary; Last Updated: 09/23/2021 Generic Medication Name Pharmacological Category (up-to-date) Formulary Brief -
Free PDF Download
European Review for Medical and Pharmacological Sciences 2012; 16: 1611-1636 The patient with chronic ischemic heart disease. Role of ranolazine in the management of stable angina A. DI MONACO, A. SESTITO Department of Cardiology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy Abstract. – Ischemic heart disease (IHD) is a serve is exhausted2. Symptom severity can be major cause of death in Western Countries and modulated by dynamic vasomotion at the site of accounts for very high costs worldwide. In this re- stenoses and/or by coronary microvascular dys- view we discussed the pathogenesis, symptoms, 1,2 diagnosis, prognosis and management of chronic function . IHD. In particular, we discussed about the percu- In microvascular angina transient myocardial taneous coronary interventions and coronary ischemia is caused by coronary microvascular artery bypass grafting, as well as to clinical trials dysfunction in patients with angiographically that evaluated the advantages of one approach normal epicardial coronary arteries, in the ab- versus another. Pharmacological treatment is 3,4 among major objectives of the review and for sence of any other specific cardiac disease . In each class of therapeutic agents an evaluation of vasospastic angina transient myocardial is- well-conducted clinical trials is provided. The chemia is caused by coronary spasm5. most important drug classes in IHD treatment are Furthermore, angina and transient myocardial betablockers, calcium channel blockers, nitrates, ischemia may also occur in patients with non ath- antiplatelet agents, and ACE-inhibitors. In addition to these agents, also new treatment options are erosclerotic obstructive coronary artery disease, evaluated in patients with stable IHD. -
Drugs Affectin the Autonomic Nervous System
Fundamentals of Medical Pharmacology Paterson Public Schools Written by Néstor Collazo, Ph.D. Jonathan Hodges, M.D. Tatiana Mikhaelovsky, M.D. for Health and Related Professions (H.A.R.P.) Academy March 2007 Course Description This fourth year course is designed to give students in the Health and Related Professions (H.A.R.P.) Academy a general and coherent explanation of the science of pharmacology in terms of its basic concepts and principles. Students will learn the properties and interactions between chemical agents (drugs) and living organisms for the rational and safe use of drugs in the control, prevention, and therapy of human disease. The emphasis will be on the fundamental concepts as they apply to the actions of most prototype drugs. In order to exemplify important underlying principles, many of the agents in current use will be singled out for fuller discussion. The course will include the following topics: ¾ The History of Pharmacology ¾ Terminology Used in Pharmacology ¾ Drug Action on Living Organisms ¾ Principles of Pharmacokinetics ¾ Dose-Response Relationships ¾ Time-Response Relationships ¾ Human Variability: Factors that will modify effects of drugs on individuals ¾ Effects of Drugs Attributable to Varying Modes of Administration ¾ Drug Toxicity ¾ Pharmacologic Aspects of Drug Abuse and Drug Dependence Pre-requisites Students must have completed successfully the following courses: Biology, Chemistry, Anatomy and Physiology, Algebra I and II Credits: 5 credits Basic Principles of Drug Action Introduction to Pharmacology a. Basic Mechanisms of Drug Actions b. Dose-response relationships c. Drug absorption d. Biotransformation of Drugs e. Pharmacokinetics f. Factors Affecting Drug Distribution g. Drug Allergy and Pharmacogenetics h. -
(12) United States Patent (10) Patent No.: US 8,080,578 B2 Liggett Et Al
USO08080578B2 (12) United States Patent (10) Patent No.: US 8,080,578 B2 Liggett et al. (45) Date of Patent: *Dec. 20, 2011 (54) METHODS FOR TREATMENT WITH 5,998.458. A 12/1999 Bristow ........................ 514,392 BUCNDOLOL BASED ON GENETIC 6,004,744. A 12/1999 Goelet et al. ...... 435/5 6,013,431 A 1/2000 Söderlund et al. 435/5 TARGETING 6,156,503 A 12/2000 Drazen et al. ..... ... 435/6 6,221,851 B1 4/2001 Feldman ... 51446 (75) Inventors: Stephen B. Liggett, Clarksville, MD 6,316,188 B1 1 1/2001 Yan et al. .......................... 435/6 6,365,618 B1 4/2002 Swartz ... 514,411 (US); Michael Bristow, Englewood, CO 6,498,009 B1 12/2002 Liggett ............................. 435/6 (US) 6,566,101 B1 5/2003 Shuber et al. 435,912 6,586,183 B2 7/2003 Drysdale et al. .................. 435/6 (73) Assignee: The Regents of the University of 6,784, 177 B2 8/2004 Cohn et al. 514,248 Colorado, a body corporate, Denver, 6,797.472 B1 9/2004 Liggett ......... ... 435/6 6,821,724 B1 1 1/2004 Mittman et al. ... 435/6 CO (US) 6,861.217 B1 3/2005 Liggett ......... ... 435/6 7,041,810 B2 5/2006 Small et al. ... ... 435/6 (*) Notice: Subject to any disclaimer, the term of this 7, 195,873 B2 3/2007 Fligheddu et al. ... 435/6 patent is extended or adjusted under 35 7,211,386 B2 5/2007 Small et al. ....... ... 435/6 7,229,756 B1 6/2007 Small et al. -
Calcium Channel Blockers in Cardiovascular Pharmacotherapy
Cardiovascular Pharmacology Core Review Journal of Cardiovascular Pharmacology and Therapeutics 2014, Vol. 19(6) 501-515 Calcium Channel Blockers in ª The Author(s) 2014 Reprints and permission: Cardiovascular Pharmacotherapy sagepub.com/journalsPermissions.nav DOI: 10.1177/1074248414530508 cpt.sagepub.com Theophile Godfraind1 Abstract This paper summarizes the pharmacological properties of calcium channel blockers (CCBs), their established therapeutic uses for cardiovascular disorders and the current improvement of their clinical effects through drug combinations. Their identification resulted from study of small molecules including coronary dilators, which were named calcium antagonists. Further experiments showed that they reduced contraction of arteries by inhibiting calcium entry and by interacting with binding sites identified on voltage-dependent calcium channels. This led to the denomination calcium channel blockers. In short-term studies, by decreasing total peripheral resistance, CCBs lower arterial pressure. By unloading the heart and increasing coronary blood flow, CCBs improve myocardial oxygenation. In long-term treatment, the decrease in blood pressure is more pronounced in hypertensive than in normotensive patients. A controversy on the safety of CCBs ended after a large antihypertensive trial (ALLHAT) sponsored by the National Heart, Lung, and Blood Institute. There are two main types of CCBs: dihydopyridine and non-dihydropyridine; the first type is vascular selective. Dihydropyrines are indicated for hypertension, chronic, stable and vasospastic angina. Non-dihydropyridines have the same indications plus antiarrythmic effects in atrial fibrillation or flutter and paroxysmal supraventricular tachycardia. In addition, CCBs reduced newly formed coronary lesions in atherosclerosis. In order to reach recommended blood pressure goals, there is a recent therapeutic move by combination of CCBs with other antihypertensive agents particularly with inhibitors acting at the level of the renin-angiotensin system. -
Medcompgx Med List
For more info, go to: MedCompGx.com Medications Conditions / Uses Other Uses CYP2C19 Anticonvulsants Lacosamide (Vimpat) Epilepsy, Seizures Phenobarbital (Luminal) Epilepsy, Seizures Barbituates, Anxiety, Sedation, Withdrawl Primidone (Mysoline) Epilepsy, Seizures Zonisamide (Zonegran) Epilepsy, Seizures Antifungals Voriconazole (Vfend) Yeast Infections, Candidiasis, Aspergillosis, Candida, Aspergillus Antidepressants Escitalopram (Lexapro) SSRI, Depression, Anxiety Citalopram (Celexa) SSRI, Depression, Anxiety OCD Sertraline (Zoloft) SSRI, Depression, Anxiety OCD, PTSD Doxepin (Silenor) Tricyclic Antidepressant, Depression Bipolar, Insomnia Imipramine (Tofranil) Tricyclic Antidepressant, Depression Trimipramine (Surmontil) Tricyclic Antidepressant, Depression Amitriptyline (Elavil) Tricyclic Antidepressant, Depression Clomipramine (Anafranil) Tricyclic Antidepressant, Depression OCD Benzodiazepines Clobazam (Onfi) Seizures Diazepam (Valium) Seizures, Muscle Spasms, Anxiety, Alcohol Withdrawl Beta Blockers Labetalol (Normodyne, Trandate) High Blood Pressure, Hypertension Immunomodulators Leflunomide (Arava) Rheumatoid Arthritis Tofacitinib (Xeljanz) Rheumatoid Arthritis Muscle Relaxants Carisoprodol (Soma) Muscle Pain, Muscle Spasms Opioids Meperidine (Demerol) Pain, Severe Pain, Narcotic, Opiate Proton Pump Inhibitors Dexlansoprazole (Dexilant) GERD, Acid Reflux, Gastric Esophageal Reflux, Ulcers, Heartburn, Zollinger-Ellison Syndrome Esomeprazole (Nexium) GERD, Acid Reflux, Gastric Esophageal Reflux, Ulcers, Heartburn, Zollinger-Ellison -
World Health Organization Model List of Essential Medicines, 21St List, 2019
World Health Organizatio n Model List of Essential Medicines 21st List 2019 World Health Organizatio n Model List of Essential Medicines 21st List 2019 WHO/MVP/EMP/IAU/2019.06 © World Health Organization 2019 Some rights reserved. This work is available under the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 IGO licence (CC BY-NC-SA 3.0 IGO; https://creativecommons.org/licenses/by-nc-sa/3.0/igo). Under the terms of this licence, you may copy, redistribute and adapt the work for non-commercial purposes, provided the work is appropriately cited, as indicated below. In any use of this work, there should be no suggestion that WHO endorses any specific organization, products or services. The use of the WHO logo is not permitted. If you adapt the work, then you must license your work under the same or equivalent Creative Commons licence. If you create a translation of this work, you should add the following disclaimer along with the suggested citation: “This translation was not created by the World Health Organization (WHO). WHO is not responsible for the content or accuracy of this translation. The original English edition shall be the binding and authentic edition”. Any mediation relating to disputes arising under the licence shall be conducted in accordance with the mediation rules of the World Intellectual Property Organization. Suggested citation. World Health Organization Model List of Essential Medicines, 21st List, 2019. Geneva: World Health Organization; 2019. Licence: CC BY-NC-SA 3.0 IGO. Cataloguing-in-Publication (CIP) data. CIP data are available at http://apps.who.int/iris. -
Rhode Island Chapter Abstracts
Rhode Island Chapter Abstracts April 1, 2015 Abdin, Ahmad Last Name: Abdin First Author: Resident First Name: Ahmad Category: Clinical Vignette PG Year: PGY-1 or MS Year: ACP Number: 2888549 Medical School or Residency Program: Warren Alpert Medical School of Brown University Hospital Affiliation: Memorial Hospital of Rhode Island, Providence VA Medical Center Additional Authors: Ahmad Abdin, MD, Mohammed Salhab, MD, Amos Charles, MD, Mazen Al-Qadi, MD Abstract Title: Amiodarone-Induced Cerebellar Dysfunction Abstract Text: Introduction: Amiodarone is a class III antiarrhythmic agent that is widely used to treat ventricular and supraventricular tachycardias. Several side-effects of the drug have been recognized including thyroid dysfunction, photosensitivity, hepatotoxicity, parenchymal lung disease, corneal deposits, and peripheral neuropathy. Cerebellar dysfunction is rarely seen in patients receiving amiodarone. We are reporting a rare case of amiodarone-induced cerebellar dysfunction that resolved completely upon discontinuation of the drug. Case Presentation: A 73-year-old man with a past medical history significant for paroxysmal atrial fibrillation, coronary artery disease, diabetes and hypertension who presented with worsening lower extremity weakness and unsteady gait with recurrent falls for the last 6 months. Two days prior to admission, his symptoms got worse and caused him to seek medical attention. Two years ago he was started and maintained on amiodarone 200 mg daily for rhythm control. On physical examination, vital signs were normal. A wide-based unsteady gait was noted. He had dysmetria bilaterally on finger-to-nose and heel-to-shin testing. The rapid alternating movements of the hands were irregular. The remainder of the general and neurologic examinations were unremarkable. -
Class I and Class III Antiarrhythmic Agents: Mechanisms of Action and the Problem of Proarrhythmic Activity
Class I and Class III Antiarrhythmic Agents: Mechanisms of Action and the Problem of Proarrhythmic Activity Vidal Essebag* * To whom correspondence should be addressed: Faculty of Medicine, McGill University, Montreal, QC, Canada H3G 1Y6 INTRODUCTION Sudden cardiac death is a leading cause of mortality in industrialized nations, accounting for 50% of all cardiovascular deaths (1). Despite a decline in the past 20 years, sudden cardiac death accounts for 300,000 fatalities per year in the United States. Approximately 60% of these deaths occur in the absence of previously diagnosed heart disease (1). Nevertheless, in most instances of sudden cardiac death, the underlying pathophysiology of atherosclerotic cardiac disease with the superimposition of transient ischemic events makes the heart more susceptible to the onset and maintenance of lethal arrhythmias (1). Approximately 50% of post-myocardial infarction (MI) fatalities are sudden cardiac deaths resulting mostly from ventricular tachycardia (VT) or ventricular fibrillation (VF). It is believed that these arrhythmias arise from mechanical dysfunction and ischemic events interacting within a disordered electrophysiologic milieu (2). This has prompted the active search for safe and effective treatment modalities and their ultimate evaluation in clinical trials. Currently, beta blockers (class II agents) are recommended for post-MI patients with frequent premature ventricular contractions (PVCs), whereas calcium antagonists (class IV agents) are not helpful, and class I agents are actually harmful (2). The benefit of class III drugs, particularly amiodarone, is presently being evaluated in large clinical trials. Therapeutic options for patients with sustained VT or VF occurring late after MI include pharmacologic antiarrhythmic therapy, transcatheter or surgical ablative therapy (for VT), and implantable cardioverter-defibrillators. -
Ukrainian Medical Stomatological Academy
Poltava State Medical University Department of Experimental and Clinical Pharmacology Lecture 9 Module 1 MEDICINAL DRUGS INFLUENCING CARDIO-VASCULAR SYSTEM. MEDICINAL DRUGS FOR TREATMENT OF ISCHEMIC HEART DISEASE. HYPOLIPIDEMIC DRUGS. ANGIOPROTECTORS Prepared by Ye.Vazhnichaya [email protected], +380666347273 CONTENTS A. Antianginal drugs 1. Pathogenesis of angina pectoris and ways to its control 2. Classification of the antianginal grugs 3. Drugs that decrease oxygen demand and increase oxygen supply 4. Drugs decreasing oxygen demand of the myocardium 5. Drugs increasing oxygen supply to the myocardium 6. Drugs increasing the myocardium stability to hypoxia B. Antiatherosclerotic drugs 1. Pathogenesis of aherosclerosis and its management 2. Classification of the antiatherosclerotic drugs 3. Hypolipidemic agents 4. Antioxidants 5. Antiplatelets 6. Angioprotectors C. Control tasks ANTIANGINAL DRUGS ISCHEMIC HEART DISEASE Ischemic heart disease Angina Myocardial Myocardial pectoris infarction sclerosis ANGINA PECTORIS Angina pectoris is characterized by a sudden, severe pressing or acute chest pain radiating to the left arm and neck. Anginal pain occurs when the oxygen supply to myocardium is insufficient for its needs. The imbalance between oxygen delivery and utilization may result from a spasm or from obstruction of heart blood vessels. The coronary blood flow is insufficient to meet the heart’s metabolic requirements. It causes the onset of anginal pain. MAIN CAUSES OF ANGINA ATTACK: thrombosis, atherosclerosis and spasm of coronary blood vessels ANTIANGINAL DRUGS: pharmacological management Pharmacological management in angina pectoris includes: Decrease in oxygen demand of myocardium Increase in oxygen supply Changes of myocardium metabolism in favor of stability to oxygen insufficiency. ANTIANGINAL DRUGS: classification A. Drugs that decrease oxygen demand of myocardium and increase oxygen supply 1. -
Child and Adolescent Psychopharmacology Manual
Southern Consortium for Children Athens, Hocking, Vinton 317 Board ADAMHS Board of Adams-Lawrence-Scioto Counties Gallia-Jackson-Meigs Board of ADAMHS Washington County MHAR Board CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY MANUAL Issued: November 2005 Compiled by: Peg Meis, M.Ed., LPCC, Director of Crisis Services Reviewed by: Edward Lynam, M.D. & Linda Adams, R.N., MSN Designed by: Jenny Metts Preface To the User: This manual has been put together for informational purposes only. It is not meant to be used for clinical practice. Each physician will have their own methodology in treating children and adolescents, as many of these drugs have not been fully tested for use with patients under the age of 18. It is strongly advised that when questions arise regarding medication for a specific youth that those questions be referred to the treating physician. • Please be aware and attuned to the possible side effects of any medication, especially at the onset of starting any new medication. • In particular, suicidal ideation with antidepressants, stimulants, and Strattera. • Watch for adverse effects of all stimulants, such as hallucinations and psychosis. It is our hope that this manual will be helpful in the field for therapists, case managers, counselors, court personnel, and child-serving agencies. We encourage you to reproduce this manual as needed and to distribute it to all staff who may benefit from its use. This manual can also be downloaded online by going to www.scchildren.com. Southern Consortium for Children Post Office Box 956 Athens, Ohio 45701 740-593-8293 Phone / 740-592-4170 Fax Contact: Peg Meis [email protected] www.scchildren.com Table of Contents ADHD Treatment Adderal.............................................................................................................