Veterinary Guide to Resistance & Parasites
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Bulletin Leading the Fight Against Heartworm Disease
BULLETIN LEADING THE FIGHT AGAINST HEARTWORM DISEASE SEPTEMBER HEARTWORM 2017 Q&A VOLUME 44 No. 3 Heartworm History: In What Year Was Heartworm First INSIDE THIS ISSUE Treated? Page 4 From the President Page 8 Research Update Abstracts from the Literature Page 14 Heartworm Hotline: Role of Heat Treatment in Diagnostics Page 19 NEW! Best Practices: Minimizing Heartworm Transmission in Relocated Dogs uestions from members, prac- published in the 1998 AHS Symposium 1 titioners, technicians, and the Proceedings. Dr. Roncalli wrote, “The Page 21 Qgeneral public are often submit- first trial to assess the efficacy of a Welcome Our New AHS ted to the American Heartworm Society microfilaricide (natrium antimonyl tar- Student Liaisons (AHS) via our website. Two of our AHS trate) was conducted some 70 years Board members, Dr. John W.McCall and ago (1927) in Japan by S. Itagaki and R. Page 25 Dr. Tom Nelson, provided the resources Makino.2 Fuadin (stibophen), a trivalent In the News: Surgeons to answer this question: In What Year antimony compound, was tested, intra- Remove a Heartworm from Was Heartworm First Treated? venously, as a microfilaricide by Popescu the Femoral Artery of a Cat The first efforts to treat canine heart- in 1933 in Romania and by W.H. Wright worm disease date back to the 1920s. Dr. and P.C. Underwood in 1934 in the USA. Page 26 Nelson referenced a review article by Dr. In 1949, I.C. Mark evaluated its use Quarterly Update Raffaele Roncalli, “Tracing the History of intraperitoneally.” What’s New From AHS? Heartworms: A 400 Year Perspective,” Continues on page 7 American Heartworm Society / PO Box 8266, Wilmington, DE 19803-8266 Become an American Heartworm Society www.heartwormsociety.org / [email protected] fan on Facebook! Follow us on Twitter! OUR GENEROUS SPONSORS PLATINUM LEVEL PO Box 8266 Wilmington, DE 19803-8266 [email protected] www.heartwormsociety.org Mission Statement The mission of the American Heartworm Society is to lead the vet- erinary profession and the public in the understanding of heartworm disease. -
Computational Studies of Drug Repurposing Targeting P-Glycoprotein Mediated Multidrug-Resistance Phenotypes in Agents of Neglect
bioRxiv preprint doi: https://doi.org/10.1101/2020.06.12.147926; this version posted June 12, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Computational studies of drug repurposing targeting P- glycoprotein mediated multidrug-resistance phenotypes in agents of neglected tropical diseases Nivedita Jaishankar 1, Sangeetha Muthamilselvan 2, Ashok Palaniappan 1,2* 1 Department of Biotechnology, Sri Venkateswara College of Engineering, Post Bag No. 1, Pennalur, Sriperumbudur Tk 602117. India 2 Department of Bioinformatics, School of Chemical and BioTechnology, SASTRA Deemed University, Thanjavur 613401. India * Corresponding author: [email protected] ABSTRACT Mammalian ABCB1 P-glycoprotein is an ATP- dependent efflux pump with broad substrate specificity associated with cellular drug resistance. Homologous to this role in mammalian biology, the P-glycoprotein of agents of neglected tropical diseases (NTDs) mediates the emergence of multidrug- resistance phenotypes. The clinical and socioeconomic implications of NTDs are exacerbated by the lack of research interest among Big Pharma for treating such conditions. This work aims to characterise P-gp homologues in certain agents of key NTDs, namely (1) Protozoa: Leishmania major, Trypanosoma cruzi; (2) Helminths: Onchocerca volvulus, Schistosoma mansoni. PSI-BLAST searches against the genome of each of these organisms confirmed the presence of P-gp homologues. Each homologue was aligned against five P- gp sequences of known structure, to identify the most suitable template based on sequence homology, phylogenetic nearest neighbor, and query coverage. -
Table of Contents Introduction
TABLE OF CONTENTS INTRODUCTION............................................................................................................. 2 DEFINITIONS .................................................................................................................. 2 ADVERSE EVENT REPORTING FOR ANIM AL DRUGS ....................................... 4 CANINE HEARTW ORM DISEASE.............................................................................. 7 M ACROCYCLIC LACTONES ...................................................................................... 8 PROHEART 6 PRODUCT INFORM ATION ............................................................... 8 REGULATORY HISTORY OF PROHEART 6 ......................................................... 10 ADE REPORTS FOR PROHEART 6 AND OTHER HEARTW ORM PREVENTIVES .............................................................................................................. 11 PROHEART 6 ADES ..................................................................................................... 16 TRENDS IN PROHEART 6 ADE REPORTING ....................................................... 19 CLINICAL M ANIFESTATIONS ................................................................................. 22 ANAPHYLAXIS/ANAPHYLACTOID REACTIONS ................................................................ 22 CONVULSIONS ................................................................................................................ 24 LIVER SIGNS.................................................................................................................. -
210867Orig1s000
CENTER FOR DRUG EVALUATION AND RESEARCH APPLICATION NUMBER: 210867Orig1s000 OTHER REVIEW(S) Clinical Inspection Summary (CIS) NDA 210867 (Moxidectin) Clinical Inspection Summary Date May 31, 2018 From John Lee, M.D., Medical Officer Janice Pohlman, M.D., M.P.H., Team Leader Kassa Ayalew, M.D., M.P.H., Branch Chief Good Clinical Practice Assessment Branch (GCPAB) Division of Clinical Compliance Evaluation (DCCE) Office of Scientific Investigations (OSI) To Kristine Park, Ph.D., Regulatory Project Manager Hiwot Hiruwy, M.D., Ph.D., Medical Officer Dmitri Iarikov, M.D., Ph.D., Clinical Team Leader Sumati Nambiar, M.D., M.P.H., Director Division of Anti-Infective Products (DAIP) Application NDA 210867 Applicant Medicines Development for Global Health (MDGH) Drug Moxidectin (trade name pending) NME Yes Review Status Priority Proposed Indication Treatment of ochocerciasis due to Onchocerca volvulus Consultation Date December 15, 2017 CIS Goal Date June 1, 2018 Action Goal Date June 13, 2018 PDUFA Due Date June 13, 2018 I. OVERALL ASSESSMENT OF FINDINGS Studies 3110A1-200-GH and 3110A1-3000-AF/ONCBL60801 were audited at good clinical practice (GCP) inspections of a clinical investigator (CI) and a contract research organization (CRO). For both inspections, the establishment inspection report (EIR) has not been received from the field office and the inspection outcome shown is based on preliminary communication with the field investigator. Both inspections revealed significant GCP deficiencies, typically (apparently) deficiencies in recordkeeping (Form FDA 483 issued at CI inspection, not issued at CRO inspection). Evidence of serious deficiencies indicative of unreliable study data was not observed and study conduct otherwise appeared GCP-compliant. -
These Ain't Your Father's Parasites: Dewormer Resistance and New Strategies for Parasite Control in Horses
These Ain't Your Father's Parasites: Dewormer Resistance and New Strategies for Parasite Control in Horses Ray M. Kaplan, DVM, PhD, DEVPC Department of Infectious Diseases College of Veterinary Medicine University of Georgia Athens, Georgia 30602 Summary Most veterinarians continue to recommend anthelmintic (dewormer) treatment programs for horses that are based on knowledge and concepts that are more than 40 years old. However, recent studies demonstrate that resistance and multiple-drug resistance in equine parasites is extremely common, but few horse owners or veterinarians take this into account when making treatment decisions. Parasites are highly over-dispersed in hosts, such that a small percentage of hosts (20%) harbor most (80%) of the parasites. The common practices of recommending the same treatment program for all horses despite great differences in parasite burdens, of recommending frequent preventive treatment of all horses without any indication of parasitic disease or knowing what species of parasites are present, of recommending the use of drugs without knowledge of their efficacy, of failing to perform fecal egg count surveillance and of failing to determine if treatments are effective, are all incompatible with achieving optimal and sustainable parasite control. Consequently, it is necessary that attitudes and approaches for parasite control in horses undergo a complete overhaul, and that both horse owners and veterinarians become educated in these important issues. Introduction The introduction of benzimidazole (BZ) anthelmintics (dewormers) led to a revolution in equine in parasite control (Drudge and Lyons 1966). With these new tools came new recommendations; horse owners were advised to deworm all horses every 8 weeks. -
Etude Rétrospective Des Déclarations D'effets Indésirables Graves Lors D
Etude rétrospective des déclarations d’effets indésirables graves lors d’utilisation d’antiparasitaires externes chez le chat et le chien Kim Schumacher To cite this version: Kim Schumacher. Etude rétrospective des déclarations d’effets indésirables graves lors d’utilisation d’antiparasitaires externes chez le chat et le chien. Médecine vétérinaire et santé animale. Université Paris-Est Créteil Val de Marne (UPEC); École nationale vétérinaire d’Alfort, 2016. Français. tel- 01874183 HAL Id: tel-01874183 https://tel.archives-ouvertes.fr/tel-01874183 Submitted on 14 Sep 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. ÉCOLE NATIONALE VÉTÉRINAIRE D’ALFORT Année 2016 ÉTUDE RÉTROSPECTIVE DES DÉCLARATIONS D’EFFETS INDÉSIRABLES GRAVES LORS D’UTILISATION D’ANTIPARASITAIRES EXTERNES CHEZ LE CHAT ET LE CHIEN THÈSE Pour le DOCTORAT VÉTÉRINAIRE Présentée et soutenue publiquement devant LA FACULTÉ DE MÉDECINE DE CRÉTEIL le…………… par Kim Charlotte Amédée SCHUHMACHER Née le 4 décembre 1991 à Vélizy-Villacoublay (Yvelines) JURY Président : Pr. Professeur à la Faculté de Médecine de CRÉTEIL Membres Directeur : M. PERROT Sébastien Maître de conférences en Pharmacologie à l’ENVA Assesseur : Mme DARMON Céline Maître de conférences en Parasitologie à l’ENVA REMERCIEMENTS Au Professeur de la Faculté de médecine de Créteil, Qui nous a fait l’honneur d’accepter la présidence de notre jury de thèse, Hommage respectueux. -
Efficacy of Albendazole and Moxidectin and Resistance To
Veterinary Parasitology 189 (2012) 387–389 Contents lists available at SciVerse ScienceDirect Veterinary Parasitology jo urnal homepage: www.elsevier.com/locate/vetpar Short communication Efficacy of albendazole and moxidectin and resistance to ivermectin against Libyostrongylus douglassii and Libyostrongylus dentatus in ostriches a a b Lara Pereira de Souza , Rosane Teixeira Lelis , Igor Rio Apa Granja , a a,∗ Renato Augusto DaMatta , Clóvis de Paula Santos a Laboratório de Biologia Celular e Tecidual, Centro de Biociências e Biotecnologia, Universidade Estadual do Norte Fluminense, 28013-602 Campos dos Goytacazes, RJ, Brazil b Rioapavestruzes, 28013-600 Guarani, MG, Brazil a r t i c l e i n f o a b s t r a c t Article history: Anthelmintic resistance has emerged globally as a problem amongst nematode of livestock Received 17 February 2012 and has been particularly well documented in equine and small ruminants. There are no Received in revised form 18 April 2012 studies regarding the efficacy of anthelmintics against the hematophagous nematodes in Accepted 20 April 2012 ostriches, Libyostrongylus dentatus; and just a few on L. douglassii. Here the efficacy of alben- dazole, ivermectin and moxidectin were evaluated against these two species in an ostrich Keywords: farm in Minas Gerais state, Brazil. The feces were collected on the day of treatment and Libyostrongylus douglassii after 13 days of an oral dose of albendazole (6 mg/kg), or an injected dose (0.2 mg/kg) of Libyostrongylus dentatus ivermectin or moxidectin. The fecal egg count reduction test and coprocultures were per- Anthelmintic resistance Ostrich formed to determine possible resistance against the drugs used. -
Parasiticides: Fenbendazole, Ivermectin, Moxidectin Livestock
Parasiticides: Fenbendazole, Ivermectin, Moxidectin Livestock 1 Identification of Petitioned Substance* 2 3 Chemical Names: 48 Ivermectin: Heart Guard, Sklice, Stomectol, 4 Moxidectin:(1'R,2R,4Z,4'S,5S,6S,8'R,10'E,13'R,14'E 49 Ivomec, Mectizan, Ivexterm, Scabo 6 5 ,16'E,20'R,21'R,24'S)-21',24'-Dihydroxy-4 50 Thiabendazole: Mintezol, Tresaderm, Arbotect 6 (methoxyimino)-5,11',13',22'-tetramethyl-6-[(2E)- 51 Albendazole: Albenza 7 4-methyl-2-penten-2-yl]-3,4,5,6-tetrahydro-2'H- 52 Levamisole: Ergamisol 8 spiro[pyran-2,6'-[3,7,1 9]trioxatetracyclo 53 Morantel tartrate: Rumatel 9 [15.6.1.14,8.020,24] pentacosa[10,14,16,22] tetraen]- 54 Pyrantel: Banminth, Antiminth, Cobantril 10 2'-one; (2aE, 4E,5’R,6R,6’S,8E,11R,13S,- 55 Doramectin: Dectomax 11 15S,17aR,20R,20aR,20bS)-6’-[(E)-1,2-Dimethyl-1- 56 Eprinomectin: Ivomec, Longrange 12 butenyl]-5’,6,6’,7,10,11,14,15,17a,20,20a,20b- 57 Piperazine: Wazine, Pig Wormer 13 dodecahydro-20,20b-dihydroxy-5’6,8,19-tetra- 58 14 methylspiro[11,15-methano-2H,13H,17H- CAS Numbers: 113507-06-5; 15 furo[4,3,2-pq][2,6]benzodioxacylooctadecin-13,2’- Moxidectin: 16 [2H]pyrano]-4’,17(3’H)-dione,4’-(E)-(O- Fenbendazole: 43210-67-9; 70288-86-7 17 methyloxime) Ivermectin: 59 Thiabendazole: 148-79-8 18 Fenbendazole: methyl N-(6-phenylsulfanyl-1H- 60 Albendazole: 54965-21-8 19 benzimidazol-2-yl) carbamate 61 Levamisole: 14769-72-4 20 Ivermectin: 22,23-dihydroavermectin B1a +22,23- 21 dihydroavermectin B1b 62 Morantel tartrate: 26155-31-7 63 Pyrantel: 22204-24-6 22 Thiabendazole: 4-(1H-1,3-benzodiazol-2-yl)-1,3- 23 thiazole -
Tutorial Article a Review of the Use of Moxidectin in Horses J
EVE 08-054 Schumacher 17/9/08 09:34 Page 2 546 EQUINE VETERINARY EDUCATION / AE / october 2008 Tutorial Article A review of the use of moxidectin in horses J. SCHUMACHER* AND J. TAINTOR Department of Clinical Sciences, J.T. Vaughan Teaching Hospital, College of Veterinary Medicine, Auburn University, Alabama, 36849-5522, USA. Keywords: horse; moxidectin; ivermectin; cyathostomins; ascarids; ectoparasites; resistance Summary which are produced naturally from soil-dwelling Streptomyces microorganisms, are divided into 2 classes of anti-parasitic Moxidectin has broad-spectrum anti-nematodal and drugs, the avermectins and the milbemycins. The first anti-arthropodal activities in the horse but is not macrocyclic lactone introduced to the equine market was the effective against tapeworms or flukes. Moxidectin and avermectin, ivermectin, which was introduced in 1981. That ivermectin have the same efficacy against internal, adult drug revolutionised control of endoparasites and ectoparasites parasites of horses. Moxidectin, however, is highly in many different species because of its relative safety and effective in eliminating encysted and hypobiotic larval efficacy against most economically important parasitic stages of cyathostomins, whereas ivermectin is not. diseases. Since the introduction of ivermectin, other Treatment of horses with moxidectin results in an egg- macrocyclic lactones have been introduced, including reappearance period (ERP) of 15–24 weeks. Because of albamectin, eprinomectin, doramectin, selamectin, moxidectin its long ERP, moxidectin is labelled to be used at and milbemycin A3/A4. Ivermectin, albamectin and 12 week intervals. Moxidectin may provide protection moxidectin are marketed for use in horses. against infection by ingested cyathostomin larvae for 2–3 weeks after it is administered. -
Sheet1 Page 1 a Abamectin Acetazolamide Sodium Adenosine-5-Monophosphate Aklomide Albendazole Alfaxalone Aloe Vera Alphadolone A
Sheet1 A Abamectin Acetazolamide sodium Adenosine-5-monophosphate Aklomide Albendazole Alfaxalone Aloe vera Alphadolone Acetate Alpha-galactosidase Altrenogest Amikacin and its salts Aminopentamide Aminopyridine Amitraz Amoxicillin Amphomycin Amphotericin B Ampicillin Amprolium Anethole Apramycin Asiaticoside Atipamezole Avoparcin Azaperone B Bambermycin Bemegride Benazepril Benzathine cloxacillin Benzoyl Peroxide Benzydamine Bephenium Bephenium Hydroxynaphthoate Betamethasone Boldenone undecylenate Boswellin Bromelain Bromhexine 2-Bromo-2-nitropan-1, 3 diol Bunamidine Buquinolate Butamisole Butonate Butorphanol Page 1 Sheet1 C Calcium glucoheptonate (calcium glucoheptogluconate) Calcium levulinate Cambendazole Caprylic/Capric Acid Monoesters Carbadox Carbomycin Carfentanil Carnidazole Carnitine Carprofen Cefadroxil Ceftiofur sodium Centella asiatica Cephaloridine Cephapirin Chlorine dioxide Chlormadinone acetate Chlorophene Chlorothiazide Chlorpromazine HCl Choline Salicylate Chondroitin sulfate Clazuril Clenbuterol Clindamycin Clomipramine Clopidol Cloprostenol Clotrimazole Cloxacillin Colistin sulfate Copper calcium edetate Copper glycinate Coumaphos Cromolyn sodium Crystalline Hydroxycobalamin Cyclizine Cyclosporin A Cyprenorphine HCl Cythioate D Decoquinate Demeclocycline (Demethylchlortetracycline) Page 2 Sheet1 Deslorelin Desoxycorticosterone Pivalate Detomidine Diaveridine Dichlorvos Diclazuril Dicloxacillin Didecyl dimethyl ammonium chloride Diethanolamine Diethylcarbamazine Dihydrochlorothiazide Diidohydroxyquin Dimethylglycine -
Pest Management Strategic Plan for Beef Cattle in Tennessee and Kentucky
Pest Management Strategic Plan for Beef Cattle in Tennessee and Kentucky Summary of Workshops held in January 2005 Princeton, KY and Nashville, TN Prepared by J. Patrick Parkman, IPM Coordinator University of Tennessee Institute of Agriculture Contact: J. Patrick Parkman (865) 974-7138 [email protected] Sponsored by the Southern Region Integrated Pest Management Center, USDA Cooperative State Research, Education and Extension Service Executive Summary With a combined total of 2,238,000 beef cows, Kentucky and Tennessee are the top two beef cattle production states east of the Mississippi. Cash receipts for cattle and calves sales in 2004 totaled $620,650,000 for Kentucky (15% of all receipts) and $514,338,000 for Tennessee (20% of all receipts). In Tennessee, cattle and calves is the leading agricultural commodity. The significance of this industry underscores the importance of reviewing the status of beef cattle pest management in these states and making recommendations for improvement. This document presents the conclusions of two one-day meetings involving producers and state Extension personnel. The meetings were held in response to regulatory actions such as the Food Quality Protection Act which may affect availability of pest management products; to the emergence of new technologies; and to ongoing and new threats to the industry such as pesticide resistance and increased pest pressure. The document includes an overview of production practices, pest incidence and importance, and current pest management practices. Arthropods are far and away the most important pest of cattle in these states, therefore, these pests are given the most emphasis. The priorities developed by meeting participants and published here should serve as a guideline to researchers, Extension personnel, regulators and industry leaders when addressing pest management issues facing beef cattle producers in Kentucky and Tennessee. -
(12) Patent Application Publication (10) Pub. No.: US 2013/0143956A1 Cady Et Al
US 2013.0143956A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2013/0143956A1 Cady et al. (43) Pub. Date: Jun. 6, 2013 (54) LONG-ACTING INJECTABLE MOXIDECTIN (22) Filed: Nov.30, 2012 FORMULATIONS AND NOVEL MOXDECTIN CRYSTAL FORMS Related U.S. Application Data (71) Applicants: Susan Mancini Cady, Yardley, PA (US); (60) Provisional application No. 61/566,336, filed on Dec. Baoqing Ma, Kendall Park, NJ (US); 2, 2011. Robert Clark Chapman, Downingtown, Publication Classification PA (US); Chunhua Yang, Edison, NJ (US); Uday Jain, Plainsboro, NJ (US) (51) Int. Cl. A6IK3I/365 (2006.01) (72) Inventors: Susan Mancini Cady, Yardley, PA (US); (52) U.S. Cl. Baoqing Ma, Kendall Park, NJ (US); CPC .................................... A61 K3I/365 (2013.01) Robert Clark Chapman, Downingtown, USPC ............................ 514/450; 549/264; 264/145 PA (US); Chunhua Yang, Edison, NJ (US); Uday Jain, Plainsboro, NJ (US) (57) ABSTRACT This invention provides for novel antiparasitic and pesticidal forms of moxidectin, including a long-acting polymeric (73) Assignee: Merial Limited, Duluth, GA (US) implant. The resulting compounds may be used in veterinary compositions which are used in treating, controlling and pre (21) Appl. No.: 13/690,185 Venting of endo- and ectoparasite infections in animals. Patent Application Publication Jun. 6, 2013 Sheet 1 of 33 US 2013/0143956 A1 FIG. I. Six: Restivati Masaaaaaaaaaaaaaaaaaaaaaaaaaaa estivate 83 3 R33 Patent Application Publication Jun. 6, 2013 Sheet 2 of 33 US 2013/0143956 A1 FIG 2A Conventional DSC of Moxidectin lot SO9060: ... -- ; : f; : : ^ ‘s 1119°C f ---. f - “r-. f a. -: ; Agree 18649°Cs f 2) skirt" ----.