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Pharmacology/Therapeutics Ii Block 1 Handouts – 2015-16
PHARMACOLOGY/THERAPEUTICS II BLOCK 1 HANDOUTS – 2015‐16 55. H2 Blockers, PPls – Moorman 56. Palliation of Contipation & Nausea/Vomiting – Kristopaitis 57. On‐Line Only – Principles of Clinical Toxicology – Kennedy 58. Anti‐Parasitic Agents – Johnson Histamine Antagonists and PPIs January 6, 2016 Debra Hoppensteadt Moorman, Ph.D. Histamine Antagonists and PPIs Debra Hoppensteadt Moorman, Ph.D. Office # 64625 Email: [email protected] KEY CONCEPTS AND LEARNING OBJECTIVES . 1 To understand the clinical uses of H2 receptor antagonists. 2 To describe the drug interactions associated with the use of H2 receptor antagonists. 3 To understand the mechanism of action of PPIs 4 To describe the adverse effects and drugs interactions with PPIs 5 To understand when the histamine antagonists and the PPIs are to be used for treatment 6 To describe the drugs used to treat H. pylori infection Drug List: See Summary Table. Histamine Antagonists and PPIs January 6, 2016 Debra Hoppensteadt Moorman, Ph.D. Histamine Antagonists and PPIs I. H2 Receptor Antagonists These drugs reduce gastric acid secretion, and are used to treat peptic ulcer disease and gastric acid hypersecretion. These are remarkably safe drugs, and are now available over the counter. The H2 antagonists are available OTC: 1. Cimetidine (Tagamet®) 2. Famotidine (Pepcid®) 3. Nizatidine (Axid®) 4. Ranitidine (Zantac®) All of these have different structures and, therefore, different side-effects. The H2 antagonists are rapidly and well absorbed after oral administration (bioavailability 50-90%). Peak plasma concentrations are reached in 1-3 hours, and the drugs have a t1/2 of 1-3 hours. H2 antagonists also inhibit stimulated (due to feeding, gastrin, hypoglycemia, vagal) acid secretion and are useful in controlling nocturnal acidity – useful when added to proton pump therapy to control “nocturnal acid breakthrough”. -
Poisoning in Children
ARTICLE IN PRESS Current Paediatrics (2005) 15, 563–568 www.elsevier.com/locate/cupe Poisoning in children Fiona JepsenÃ, Mary Ryan Emergency Medicine, Royal Liverpool Children’s NHS Trust, Alder Hey, Liverpool L12 2AP, UK KEYWORDS Summary Poisoning accounts for about 7% of all accidents in children under 5 Poisoning; years and is implicated in about 2% of all childhood deaths in the developed world, Child; and over 5% in the developing world (National Poisons Information Service). In Accidents; considering this topic, however, it is important to differentiate accidental overdose Home (common in the younger age groups) and deliberate overdose (more common in young adults). Although initial assessment and treatment of these groups may not differ significantly, the social issues and ongoing follow-up of these children will be totally different and the treating physician must remain aware of this difference. The initial identification and treatment of these children remains the mainstay of management, and many ingested substances do not have a specific antidote. Supportive treatment must be planned and the potential for delayed or long-term effects noted. The specific presentation and treatment of some of the commonly ingested substances will be addressed in this article, and guidance given on when to contact expert help. & 2005 Elsevier Ltd. All rights reserved. Introduction such as bleaches, detergents and turpentine sub- stitutes. More than 100 000 individuals are admitted to Toxic compounds may be ingested or inhaled hospital in England and Wales annually due to either accidentally or deliberately. Accidental poisoning, accounting for 10% of all acute admis- poisoning can occur at any age, but is much more 1 sions.1 However, the true incidence of acute common in children. -
WSAVA List of Essential Medicines for Cats and Dogs
The World Small Animal Veterinary Association (WSAVA) List of Essential Medicines for Cats and Dogs Version 1; January 20th, 2020 Members of the WSAVA Therapeutic Guidelines Group (TGG) Steagall PV, Pelligand L, Page SW, Bourgeois M, Weese S, Manigot G, Dublin D, Ferreira JP, Guardabassi L © 2020 WSAVA All Rights Reserved Contents Background ................................................................................................................................... 2 Definition ...................................................................................................................................... 2 Using the List of Essential Medicines ............................................................................................ 2 Criteria for selection of essential medicines ................................................................................. 3 Anaesthetic, analgesic, sedative and emergency drugs ............................................................... 4 Antimicrobial drugs ....................................................................................................................... 7 Antibacterial and antiprotozoal drugs ....................................................................................... 7 Systemic administration ........................................................................................................ 7 Topical administration ........................................................................................................... 9 Antifungal drugs ..................................................................................................................... -
Critical Care Nursing of Infants and Children Martha A
University of Pennsylvania ScholarlyCommons Miscellaneous Papers Miscellaneous Papers 1-1-2001 Critical Care Nursing of Infants and Children Martha A. Q. Curley University of Pennsylvania, [email protected] Patricia A. Moloney-Harmon The Children's Hospital at Sinai Copyright by the author. Reprinted from Critical Care Nursing of Infants and Children, Martha A.Q. Curley and Patricia A. Moloney-Harmon (Editors), (Philadelphia: W.B. Saunders Co., 2001), 1,128 pages. NOTE: At the time of publication, the author, Martha Curley was affiliated with the Children's Hospital of Boston. Currently, she is a faculty member in the School of Nursing at the University of Pennsylvania. This paper is posted at ScholarlyCommons. http://repository.upenn.edu/miscellaneous_papers/4 For more information, please contact [email protected]. Please Note: The full version of this book and all of its chapters (below) can be found on ScholarlyCommons (from the University of Pennsylvania) at http://repository.upenn.edu/miscellaneous_papers/4/ Information page in ScholarlyCommons Full book front.pdf - Front Matter, Contributors, Forward, Preface, Acknowledgements, and Contents Chapter 1.pdf - The Essence of Pediatric Critical Care Nursing Chapter 2.pdf - Caring Practices: Providing Developmentally Supportive Care Chapter_3.pdf - Caring Practices: The Impact of the Critical Care Experience on the Family Chapter_4.pdf - Leadership in Pediatric Critical Care Chapter 5.pdf - Facilitation of Learning Chapter_6.pdf - Advocacy and Moral Agency: A Road Map for -
Chelation Therapy
Corporate Medical Policy Chelation Therapy File Name: chelation_therapy Origination: 12/1995 Last CAP Review: 2/2021 Next CAP Review: 2/2022 Last Review: 2/2021 Description of Procedure or Service Chelation therapy is an established treatment for the removal of metal toxins by converting them to a chemically inert form that can be excreted in the urine. Chelation therapy comprises intravenous or oral administration of chelating agents that remove metal ions such as lead, aluminum, mercury, arsenic, zinc, iron, copper, and calcium from the body. Specific chelating agents are used for particular heavy metal toxicities. For example, desferroxamine (not Food and Drug Administration [FDA] approved) is used for patients with iron toxicity, and calcium-ethylenediaminetetraacetic acid (EDTA) is used for patients with lead poisoning. Note that disodium-EDTA is not recommended for acute lead poisoning due to the increased risk of death from hypocalcemia. Another class of chelating agents, called metal protein attenuating compounds (MPACs), is under investigation for the treatment of Alzheimer’s disease, which is associated with the disequilibrium of cerebral metals. Unlike traditional systemic chelators that bind and remove metals from tissues systemically, MPACs have subtle effects on metal homeostasis and abnormal metal interactions. In animal models of Alzheimer’s disease, they promote the solubilization and clearance of β-amyloid protein by binding to its metal-ion complex and also inhibit redox reactions that generate neurotoxic free radicals. MPACs therefore interrupt two putative pathogenic processes of Alzheimer’s disease. However, no MPACs have received FDA approval for treating Alzheimer’s disease. Chelation therapy has also been investigated as a treatment for other indications including atherosclerosis and autism spectrum disorder. -
Compatibility Mode
11/16/2010 DIURETIK Diuretik & Anti-Diuretik VOLUME URINE Dept. Farmakologi dan Terapeutik, Fakultas Kedokteran Universitas Sumatera Utara ANTI DIURETIK PENGHAMBAT Classes of Diuretics: DIURETIK KARBONIK OSMOTIK Definitions ANHIDRASE Diuretic: • substance that promotes the DIURETIKDIURETIK excretion of urine DIURETIK DIURETIK HEMAT Natriuretic: KUAT KALIUM • substance that promotes the renal excretion of sodium TIAZID 1 11/16/2010 Diuretik osmotik Osmotic Diuretic Osmotic Diuretic Mechanism of Action: Characteristics Inhibition of Water Diffusion • Oral absorption: ( - ), parenteral • Free filtration in osmotically active administration concentration • Freely filterable • Osmotic pressure of non-reabsorbable solute prevents water reabsorption and • Little or no tubular reabsorption increase urine volume • Inert or non-reactive – Proximal tubule • Resistant to degradation by tubules – Thin limb of the loop of Henle 2 11/16/2010 Therapeutic Uses Osmotic Diuretics in Current Use Prophylaxis of renal failure • Mannitol (prototype) Mechanism: • Urea • Drastic reductions in GFR cause dramatically increased proximal tubular • Glycerin water reabsorption and a large drop in urinary excretion • Isosorbide • Osmotic diuretics are still filtered under these conditions and retain an equivalent amount of water, maintaining urine flow Therapeutic Uses (Cont.) Toxicity of Osmotic Diuretics • Increased extracellular fluid volume Reduction of pressure in extravascular fluid compartments • Hypersensitivity reactions • Glycerin metabolism can lead to • -
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 -
3.5 3.6 Rangan Metals Metalloids New Orleans
Metals/Metalloids Metals and Metalloids Cyrus Rangan MD, FAAP, ACMT Los Angeles County Department of Public Health California Poison Control System Childrens Hospital Los Angeles 1 Treatment of Metal Poisoning Old School Approaches “The treatment of acute [insert metal here]-poisoning consists in the evacuation of the stomach, if necessary, the exhibition of the sulphate of sodium or of magnesium, and the meeting of the indications as they arise. The Epsom and Glauber’s salts act as chemical antidotes, by precipitating the insoluble sulphate of [insert metal here], and also, if in excess, empty the bowel of the compound formed. To allay gastrointestinal irritation, albuminous drinks should be given and opium freely exhibited…” Wood, HC: Therapeutics Materia Medica and Toxicology, 1879 2 Treatment of Metal Poisoning Old School Approaches “If possible, the rapid administration of 2 oz. (6-7 heaping teaspoonfuls) of Magnesium sulfate (Epsom Salts) or Sodium sulfate (Glauber’s Salt) in plenty of water. Alum (aluminum potassium sulfate) will also be useful in 4 gm (60 gr.) doses (dissolved) repeated. Very dilute Sulfuric acid may be employed (30 cc of a 10 % solution diluted to 1 quart). All soluble sulfates precipitate [metal] as an insoluble sulfate…” Lucas, GW: The Symptoms and Treatment of Acute Poisoning; 1953 3 1 Metals/Metalloids Overview of Metals • Iron • Lead • Arsenic • Mercury • … a whole bunch of other ones 4 What’s a Metal? What’s a Metalloid? 5 Iron Poisoning Introduction • Essential for normal tissue and organ function • In toxic doses, iron salts (ferrous sulfate, fumarate or gluconate) cause corrosive gastrointestinal effects followed by hypotension, metabolic acidosis, and multisystem failure. -
Sign up to Receive ATOTW Weekly – Email [email protected]
Sign up to receive ATOTW weekly – email [email protected] ACCIDENTAL POISONING IN CHILDREN ANAESTHESIA TUTORIAL OF THE WEEK 95 9TH JUNE 2008 Dr Susara Ribbens Specialist Registrar North Central London School of Anaesthetics [email protected] Introduction Poisoning is a significant global public health problem. According to the World Health Organisation data, an estimated 350 000 people died from unintentional poisoning in 2002. Accidental poisoning occurs most often in the age group 1-5 years although less than one per cent of poisoning in children is serious. More than 94% of fatal poisonings occur in low- and middle-income countries. It remains a challenge to identify those at risk at an early stage. Education of the general public and also the provision of child-proof containers for household chemicals and medicines play a key role in prevention. (Toxic plants, insect and snake bites are not discussed in this tutorial, but see www.rch.org.au/poisons for more information) Questions True or false: 1. Emesis or nasogastric aspiration are indicated after sodium hydroxide ingestion. 2. Regarding paraffin ingestion – abnormalities on the chest film may be seen in the absence of symptoms. 3. A fever after paraffin ingestion is always due to a secondary infection. 4. Ingestion of small amounts of paraquat is usually harmless. 5. High FiO2 should be avoided in paraquat ingestion to prevent pulmonary fibrosis. 6. Organophosphate forms an irreversible complex with cholinesterase. 7. Carbon monoxide is irritant with a distinctive odour. 8. The SpO2 reading in carbon monoxide poisoning is usually less than 85%. 9. A plasma paracetamol level should be taken within 2 hours of ingestion. -
Evaluation of Poisoning and Drug Overdose
Evaluation of Poisoning and Drug Overdose Kara Lynch, PhD, DABCC University of California San Francisco San Francisco, CA Learning Objectives • Understand the laboratories role in the diagnosis and treatment of toxicology cases • Review the pathophysiology of toxic exposures • Identify the common toxidromes • Calculate the osmolar gap and anion gap • Be able to recognize drug overdoses Paraclesus – “father of toxicology” • “All things are poison, and nothing is without poison; only the dose permits something not to be poisonous.” • “The dose makes the poison.” • substances considered toxic are harmless in small doses, and an ordinarily harmless substance can be deadly if over-consumed Paraclesus, 1490 - 1541 Definition of “Poisoning” • A poisoning occurs when a person’s exposure to a natural or manmade substance has an undesirable effect - CDC • Poisonings can be classified as: – Self-harm or suicide – Assault or homicide – Unintentional or accidental, when no harm was intended – includes overdoses resulting from drug misuse, drug abuse or taking too much of a drug for medical reasons Monitoring Poisonings • AAPCC – American Association of Poison Control Centers – – National poison data system (NPDS) annual report • DAWN – Drug Abuse Warning Network • SAMHSA World Drug Report – Substance Abuse and Mental Health Services Administration • CDC – Center for Disease Control – National Vital Statistics System (NVSS) Poisoning / Overdose Trends Poisoning / Overdose Trends AAPCC: Top 25 human exposures AAPCC: Top 25 pediatric exposures Increase -
Presented By: Dr. Joohee Pradhan Assistant Professor Department of Pharmaceutical Sciences, MLSU, Udaipur
Presented By: Dr. Joohee Pradhan Assistant Professor Department of Pharmaceutical Sciences, MLSU, Udaipur OUTLINE • Introduction and Definition • Relevant Physiology of Urine Formation • Classification: different ways • Carbonic anhydrase inhibitors: Acetazolamide*, Methazolamide, Dichlorphenamide. • Thiazides: Chlorthiazide*, Hydrochlorothiazide, Hydroflumethiazide, Cyclothiazide, • Loop diuretics: Furosemide*, Bumetanide, Ethacrynic acid. • Potassium sparing Diuretics: Spironolactone, Triamterene, Amiloride. • Osmotic Diuretics: Mannitol 2 Introduction and Definition • Diuretics (natriuretics) are drugs which cause a net loss of Na+ and water in urine and hence increase the urine output (or) urine volume. • The primary action of most diuretics is the direct inhibition of Na+ reabsorption (increased excretion) at one or more of the four major sites along the nephron. • An increased Na+ excretion is accompanied by anion like Cl- Since NaCl is the major determinant of extracellular fluid volume; Diuretics reduce extracellular fluid volume (decrease in oedema) by decreasing total body NaCl content. 3 Introduction and Definition • Diuretics are very effective in the treatment of conditions like: o chronic heart failure o nephrotic syndrome o chronic hepatic diseases o hypertension o Pregnancy associated oedema o Cirrhosis of the liver. 4 Relevant Physiology of Urine Formation • Kidneys are the organs responsible for urine formation. Two important functions of the kidney are: o To maintain a homeostatis balance of electrolytes and water. o To excrete water soluble end products of metabolites. • Each kidney contains approximately one million nephrons and is capable of forming urine independently. • Urine formation starts from glomerular filtration (g.f.) in a prodigal way. • Normally, about 180 L of fluid is filtered everyday: all soluble constituents of blood minus the plasma proteins (along with substances bound to them) and lipids, are filtered at the glomerulus. -
Poisoning and Animal Bites
Poisoning and animal bites ผศ.นพ.วรพันธ์ เกรียงสุนทรกิจ กุมารเวชศาสตร์ผู้ป่วยนอก ภาควิชากุมารเวชศาสตร์ คณะแพทยศาสตร์ศิริราชพยาบาล Toxicology “All substances are poisons; there is none which is not a poison. The right dose differentiates a poison from a remedy.” Paracelsus, early 1500s Scope of talk •Common drugs and chemical agents in the house •Lead exposure •Snake bite •How to prevent chemical and drugs poisoning •First aid for poisoning and snake bite Poisoning in children •Toddlers and young children are explorers and have much hand-mouth activity •Incidence of poisoning increases after 9- month old •Over 90% of poisoning exposures occur in homes •Unintentional exposure: young children (less than 6 yr)> older children Rate of human poison exposures by age group Acute poisoning surveillance in Thailand: the current state of affairs and a vision for the future, Emergency Medicine, 2013 Iron supplement • Almost 16,000 iron exposures/ year: reported in children < 6 years of age in the US • Serious toxicity: adult preparation > chewable vitamins with iron • Prenatal and postnatal iron supplement: increase risk of poisoning in older sibling • 4-time increase in the risk of iron poisoning to the older sibling of a newborn during the first postpartum month. Iron poisoning in young children: association with the birth of a sibling. CMAJ. 2003;168:1539–1542. Clinical presentation • Gastrointestinal (GI) phase: 30 minutes to 6 hours after ingestion • Latent, or relative stability, phase: 6 to 24 hours after ingestion • Shock and metabolic acidosis: