Evaluation of the Efficacy of Doramectin in the Control Of
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)&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 -
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 -
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 -
(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" ----. -
Alpaca and Llama Parasite Treatment
Alpaca and Llama Parasite Treatment Albendazole (Valbazen) 10mg/kg Do not recommend in pregnancy or for young crias! Much better for killing tapeworms than Fenbendazole. Give orally - 6cc/100 pounds of body weight. Give one dose once per day for three days in a row (max). May need to repeat in two weeks depending on parasite load. May also have an ovacidal effect – meaning that it kills eggs and thus prevents pasture contamination – therefore it is good for isolation pens. Doramectin (Dectomax) 1cc/50 pounds of body weight every 8 weeks. Or give 1cc/70 pounds of body weight every 6 weeks. Give SubQ. (Recommend 20 gauge needle) Primarily for Meningeal Worm prevention. May kill some strongyles. Probably ineffective against most Nematodirus and Trichuris. Ivermectin (Ivomec) 1cc/70 pounds of body weight for Meningeal Worm prevention. Note that efficacy lasts for no more than 4 weeks max! Excellent for mange treatment: Dose at 1cc/50 pounds for mange – 3 days in row, and then repeat one dose in one week. Do not give mange treatment to pregnant females within first 60 days of pregnancy! Give SubQ. (Recommend 20 gauge needle) Probably ineffective in llamas and alpacas for Trichuris, Nematodirus, Moniezia, some strongyles, and liver flukes. You can purchase Ivomec Plus to kill liver flukes. Fenbendazole (Panacur or Safeguard) 20mg/kg or 1cc/10 pounds of body weight Give orally three days in row for Nematodirus. Give orally 5 days in a row and repeat in 2 weeks for Trichuris and Moneizia (tapeworms). This is a very safe drug, even for very young crias and newly pregnant females! Levamisole 8mg/kg Oral drug is safer than the injectible version. -
Federal Register / Vol. 60, No. 80 / Wednesday, April 26, 1995 / Notices DIX to the HTSUS—Continued
20558 Federal Register / Vol. 60, No. 80 / Wednesday, April 26, 1995 / Notices DEPARMENT OF THE TREASURY Services, U.S. Customs Service, 1301 TABLE 1.ÐPHARMACEUTICAL APPEN- Constitution Avenue NW, Washington, DIX TO THE HTSUSÐContinued Customs Service D.C. 20229 at (202) 927±1060. CAS No. Pharmaceutical [T.D. 95±33] Dated: April 14, 1995. 52±78±8 ..................... NORETHANDROLONE. A. W. Tennant, 52±86±8 ..................... HALOPERIDOL. Pharmaceutical Tables 1 and 3 of the Director, Office of Laboratories and Scientific 52±88±0 ..................... ATROPINE METHONITRATE. HTSUS 52±90±4 ..................... CYSTEINE. Services. 53±03±2 ..................... PREDNISONE. 53±06±5 ..................... CORTISONE. AGENCY: Customs Service, Department TABLE 1.ÐPHARMACEUTICAL 53±10±1 ..................... HYDROXYDIONE SODIUM SUCCI- of the Treasury. NATE. APPENDIX TO THE HTSUS 53±16±7 ..................... ESTRONE. ACTION: Listing of the products found in 53±18±9 ..................... BIETASERPINE. Table 1 and Table 3 of the CAS No. Pharmaceutical 53±19±0 ..................... MITOTANE. 53±31±6 ..................... MEDIBAZINE. Pharmaceutical Appendix to the N/A ............................. ACTAGARDIN. 53±33±8 ..................... PARAMETHASONE. Harmonized Tariff Schedule of the N/A ............................. ARDACIN. 53±34±9 ..................... FLUPREDNISOLONE. N/A ............................. BICIROMAB. 53±39±4 ..................... OXANDROLONE. United States of America in Chemical N/A ............................. CELUCLORAL. 53±43±0 -
01 Front.Pdf (2.451Mb)
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. VETERINARY ANTHELMINTICS: THEIR EFFICACY AND EFFECTS ON ABOMASAL PHYSIOLOGY A thesis presented in partial fulfilment of the requirements for the degree of MASTER OF VETERINARY SCIENCE in Veterinary Clinical Pharmacology at Massey University NICHOLAS CHARLES WHELAN March 1998 For Pauline, with all my love iii ABSTRACT PART 1. A Review of the Veterinary Anthelmintic Literature A comprehensive review was undertaken of the pharmacology, efficacy, side effects and toxicity of veterinary anthelmintics used against nematode parasites. Anthelmintics reviewed for use in cattle, sheep, goats, horses, dogs and cats include copper, nicotine, arsenic, tetrachlorethylene, phenothiazine, diethylcarbamazine, piperazine, toluene, cyacethydrazide, bephenium, thenium, organophosphates, and methyridine. The review was limited to cattle for the benzimidazoles, pyrantel, morantel, tetramisole, levamisole, avermectin and milbemycins anthelmintics. Efficacy data is provided in a tabular format which classifies each anthelmintic according to method of administration and dose. PART2 Efficacy of two formulations of moxidectin pour-on and the effects of treatment on serum pepsinogen and gastrin levels and tissue gastrin in cattle Three groups of eight yearling Friesian bulls were used to compare the efficacy of two 5 g/L pour-on formulations of moxidectin applied at 1ml/10kg (500 mcg moxidectin per kg bodyweight) in removing naturally acquired gastrointestinal parasites. At slaughter, 14-16 days after treatment, the burdens of Ostertagia spp. and Trichostrongylus axei were significantly lower in both the treated groups versus the controls (P<0.01 ). -
Feedlot Gastrointestinal Parasite Control and Anthellllintic Treatment Options, a Review
PEER REVIEWED Feedlot gastrointestinal parasite control and anthellllintic treatment options, a review Matthew D. Edmonds, DVM, PhD; Edward G. Johnson, DVM; Jenifer D. Edmonds, DVM, PhD Johnson Research, LLC, Parma, ID 83660 Corresponding author: Dr. Jenifer Edmonds, Tel.: 208-722-5829, Email address:[email protected] Abstract efficacious anthelmintics for the feedlot industry is well recognized. Typically, when compared to non-treated con Anthelmintics are an important tool in the feedlot trols, deworming can be expected to improve dry matter industry. The goal of this review article is to provide intake, feed efficiency, and weight gain. Often an improve the veterinary practitioner with a short summary ment in carcass quality is also observed with anthelmintic of the important aspects of internal gastrointestinal treatment. This treatment effect was shown in a single parasite control in the feedlot. A review of economically feedlot trial with over 6000 heavyweight yearling steers.10 significant gastrointestinal nematodes and the bovine In this study, treatment with an injectable avermectin at liver fluke is provided, along with a discussion of treat feedlot entry was associated with statistically significant ment options and an anthelmintic efficacy assessment. improvements in average daily gain (ADG), dry matter Important aspects unique to the feedlot environment intake, feed efficiency, and carcass grading when com are addressed, including anthelmintic resistance and pared to negative controls. combination anthelmintic therapies. Bovine Nematodes Key words: bovine, feedlot, parasitology, anthelmintic, gastrointestinal nematodes, flukes Important abomasal nematode parasites offeedlot cattle include Ostertagia ostertagi, Haemonchus placei, Resume and Trichostrongylus axei. In terms of relative clinical importance, 0. ostertagi is considered the most impor Les anthelminthiques sont des outils importants tant helminth parasite of cattle in the United States.2 pour l'industrie des pares d'engraissement. -
IJP: Drugs and Drug Resistance 10 (2019) 69–83
IJP: Drugs and Drug Resistance 10 (2019) 69–83 Contents lists available at ScienceDirect IJP: Drugs and Drug Resistance journal homepage: www.elsevier.com/locate/ijpddr Perspectives on the utility of moxidectin for the control of parasitic nematodes in the face of developing anthelmintic resistance T ∗ ∗∗ Roger K. Prichard , Timothy G. Geary Institute of Parasitology, McGill University, Sainte Anne-de-Bellevue, Quebec, Canada, H9X3V9 ARTICLE INFO ABSTRACT Keywords: Macrocyclic lactone (ML) anthelmintics are the most important class of anthelmintics because of our high de- Moxidectin pendence on them for the control of nematode parasites and some ectoparasites in livestock, companion animals Milbemycin and in humans. However, resistance to MLs is of increasing concern. Resistance is commonplace throughout the Ivermectin world in nematode parasites of small ruminants and is of increasing concern in horses, cattle, dogs and other Avermectin animals. It is suspected in Onchocerca volvulus in humans. In most animals, resistance first arose to the aver- Macrocyclic lactone resistance mectins, such as ivermectin (IVM), and subsequently to moxidectin (MOX). Usually when parasite populations Nematode are ML-resistant, MOX is more effective than avermectins. MOX may have higher intrinsic potency against some parasites, especially filarial nematodes, than the avermectins. However, it clearly has a significantly different pharmacokinetic profile. It is highly distributed to lipid tissues, less likely to be removed by ABC efflux trans- porters, is poorly metabolized and has a long half-life. This results in effective concentrations persisting for longer in target hosts. It also has a high safety index. Limited data suggest that anthelmintic resistance may be overcome, at least temporarily, if a high concentration can be maintained at the site of the parasites for a prolonged period of time. -
Comparison of the Environmental Properties of Parasiticides and Harmonisation of the Basis for Environmental Assessment at the EU Level
Environmental Research of the Federal Ministry for the Environment, Nature Conservation, Building and Nuclear Safety Project number: 3714 64 410 0 Report number: [entered by the UBA library] Comparison of the environmental properties of parasiticides and harmonisation of the basis for environmental assessment at the EU level by Jörg Römbke, Karen Duis, Philipp Egeler, Daniel Gilberg, Christine Schuh ECT Oekotoxikologie GmbH, Böttgerstr. 2-14, D-65439 Flörsheim Monika Herrchen, Dieter Hennecke Fraunhofer-Institute for Molecular Biology and Applied Ecology, Auf dem Aberg 1, D-57392 Schmallenberg Ludwig E. Hölzle, Brigitte Heilmann-Thudium University of Hohenheim, Livestock Infectiology and Environmental Hygiene, Garbenstr. 30, D-70599 Stuttgart Manuel Wohde, Julia Wagner, Rolf-Alexander Düring Justus Liebig University, Institute for Soil Science and Soil Conservation, Heinrich Buff-Ring 26, D-35392 Gießen On behalf of the German Environment Agency Completion date: May 2018 Comparison of the environmental properties of parasiticides and harmonisation of the basis for environmental assessment at the EU level Abstract Avermectin and milbemycin parasiticides have a high toxicity to non-target organisms, are often per- sistent and may have a potential to bioaccumulate. The present project contributes to filling gaps in the database for a complete environmental risk assessment of these parasiticides. In addition, risk management strategies for parasiticides used in pasture animals were discussed. For ivermectin and selamectin, log POW values of 5.6 and 6.0 were derived, respectively. In studies with zebrafish, biocon- centration factors of 63–111 for ivermectin and 70–71 for doramectin (based on total radio-active residues, normalised to a 5% lipid content) were determined. -
Arzneimittelrückstände in Der Umwelt
Arzneimittelrückstände in der Umwelt ARZNEIMITTELRÜCKSTÄNDE IN DER UMWELT Christina Hartmann REPORT REP-0573 Wien 2016 Projektleitung Sigrid Scharf AutorInnen Christina Hartmann Mitarbeit Manfred Clara Sigrid Scharf Monika Denner Übersetzung Brigitte Read Lektorat Maria Deweis Satz/Layout Manuela Kaitna Umschlagphoto © gunnar3000 – Fotolia.com Weitere Informationen zu Umweltbundesamt-Publikationen unter: http://www.umweltbundesamt.at/ Impressum Medieninhaber und Herausgeber: Umweltbundesamt GmbH Spittelauer Lände 5, 1090 Wien/Österreich Eigenvervielfältigung Das Umweltbundesamt druckt seine Publikationen auf klimafreundlichem Papier. © Umweltbundesamt GmbH, Wien, 2016 Alle Rechte vorbehalten ISBN 978-3-99004-386-8 Arzneimittelrückstände in der Umwelt – Inhalt INHALT ZUSAMMENFASSUNG .......................................................................... 7 SUMMARY .............................................................................................. 8 1 EINLEITUNG ........................................................................................... 9 2 DURCHFÜHRUNG ............................................................................... 10 3 HUMANARZNEIMITTEL ...................................................................... 11 3.1 Begriffsbestimmungen lt. Arzneimittelgesetz (AMG) ...................... 11 3.2 ATC-Klassifizierung ............................................................................ 11 3.3 Pharmakokinetik ................................................................................. 12 -
Repurposing Avermectins and Milbemycins Against Mycobacteroides Abscessus and Other Nontuberculous Mycobacteria
antibiotics Article Repurposing Avermectins and Milbemycins against Mycobacteroides abscessus and Other Nontuberculous Mycobacteria Lara Muñoz-Muñoz 1,2,*, Carolyn Shoen 3, Gaye Sweet 4, Asunción Vitoria 1,2, Tim J. Bull 5 , Michael Cynamon 3, Charles J. Thompson 4 and Santiago Ramón-García 1,6,7,* 1 Department of Microbiology, Faculty of Medicine, University of Zaragoza, 50009 Zaragoza, Spain; [email protected] 2 Microbiology Unit, Clinical University Hospital Lozano Blesa, 50009 Zaragoza, Spain 3 State University of New York Upstate Medical Center, Syracuse, NY 13210, USA; [email protected] (C.S.); [email protected] (M.C.) 4 Department of Microbiology and Immunology, Centre for Tuberculosis Research, Life Sciences Institute, University of British Columbia, Vancouver, BC V6T 1Z3, Canada; [email protected] (G.S.); [email protected] (C.J.T.) 5 Institute for Infection & Immunity, St. George’s University of London, London SW17 0RE, UK; [email protected] 6 Research & Development Agency of Aragón (ARAID) Foundation, 50018 Zaragoza, Spain 7 CIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, 28029 Madrid, Spain * Correspondence: [email protected] (L.M.-M.); [email protected] (S.R.-G.) Citation: Muñoz-Muñoz, L.; Shoen, Abstract: Infections caused by nontuberculous mycobacteria (NTM) are increasing worldwide, C.; Sweet, G.; Vitoria, A.; Bull, T.J.; resulting in a new global health concern. NTM treatment is complex and requires combinations of Cynamon, M.; Thompson, C.J.; several drugs for lengthy periods. In spite of this, NTM disease is often associated with poor treatment Ramón-García, S. Repurposing outcomes. The anti-parasitic family of macrocyclic lactones (ML) (divided in two subfamilies: Avermectins and Milbemycins avermectins and milbemycins) was previously described as having activity against mycobacteria, against Mycobacteroides abscessus and including Mycobacterium tuberculosis, Mycobacterium ulcerans, and Mycobacterium marinum, among Other Nontuberculous Mycobacteria.