Community Use of Antibiotics
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Antibiotic Therapy of Cholera in Children,*
Bull. Org. mond. Santo 1967, 37, 529-538 Bull. Wld filth Org. Antibiotic Therapy of Cholera in Children,* JOHN LINDENBAUM,1 WILLIAM B. GREENOUGH 2 & M. R. ISLAM In a controlled trial of the effects of oral antibiotics in treating cholera in children in Dacca, East Pakistan, tetracycline was the most effective of 4 antibiotics tested in reducing stool volume, intravenous fluid requirement, and the duration of diarrhoea and positive stool culture. Increasing the duration of tetracycline therapy from 2 to 4 days, or increasing the total dose administered, resulted in shorter duration ofpositive culture, but did not affect stool volume or duration ofdiarrhoea. Only I % of the children receiving tetracycline had diarrhoea for more than 4 days. Tetracycline was significantly more effective than intravenous fluid therapy alone, regardless of severity of disease. Chloramphenicol, while also effective, was inferior to tetracycline. Streptomycin and paromomycin exerted little or no effect on the course of illness or duration of positive culture. Therapeutic failures with these drugs were not due to the development ofbacterial resistance. From these findings, tetracycline appears to be the drug of choice against Vibrio cholerae infection in children. Oral therapy for 48 hours is effective clinically, but is associated with 20% bacteriological relapses when the drug is discontinued; it is not known whether extending the therapy for a week or more would eliminate such relapses. In recent years several groups have conducted replacement was compared with treatment with clinical trials of antibiotic therapy in adult patients intravenous fluids only. with cholera (Greenough et al., 1964; Carpenter et al., 1966; Uylangco et al., 1965, 1966; Kobari, METHODS AND MATERIALS 1965; Lindenbaum et al., 1967). -
Early-Life Antibiotic Use and Risk of Asthma and Eczema: Results of a Discordant Twin Study
Early View Original article Early-life antibiotic use and risk of asthma and eczema: results of a discordant twin study Elise M.A. Slob, Bronwyn K. Brew, Susanne J.H. Vijverberg, Chantal J.A.R. Kats, Cristina Longo, Mariëlle W. Pijnenburg, Toos C.E.M. van Beijsterveldt, Conor V. Dolan, Meike Bartels, Patrick Magnusson, Paul Lichtenstein, Tong Gong, Gerard H. Koppelman, Catarina Almqvist, Dorret I. Boomsma, Anke H. Maitland-van der Zee Please cite this article as: Slob EMA, Brew BK, Vijverberg SJH, et al. Early-life antibiotic use and risk of asthma and eczema: results of a discordant twin study. Eur Respir J 2020; in press (https://doi.org/10.1183/13993003.02021-2019). This manuscript has recently been accepted for publication in the European Respiratory Journal. It is published here in its accepted form prior to copyediting and typesetting by our production team. After these production processes are complete and the authors have approved the resulting proofs, the article will move to the latest issue of the ERJ online. Copyright ©ERS 2020 Early-life antibiotic use and risk of asthma and eczema: results of a discordant twin study Elise M.A. Slob1,2 Bronwyn K. Brew3,4 Susanne J.H. Vijverberg1,2 Chantal J.A.R. Kats1 Cristina Longo1 Mariëlle W. Pijnenburg5 Toos C.E.M. van Beijsterveldt6 Conor V. Dolan6 Meike Bartels6 Patrick Magnusson3 Paul Lichtenstein3 Tong Gong3 Gerard H. Koppelman7,8 Catarina Almqvist3,9 Dorret I. Boomsma6 Anke H. Maitland-van der Zee1,2* 1. Department of Respiratory Medicine, Amsterdam University Medical Centers, University of Amsterdam, P.O. -
Case 2:17-Cv-03768-CMR Document 3-1 Filed 10/31/17 Page 1 of 243
Case 2:17-cv-03768-CMR Document 3-1 Filed 10/31/17 Page 1 of 243 UNITED STATES DISTRICT COURT EASTERN DISTRICT OF PENNSYLVANIA IN RE: GENERIC PHARMACEUTICALS MDL 2724 PRICING ANTITRUST LITIGATION 16-MD-2724 ____________________________________ HON. CYNTHIA M. RUFE IN RE: STATE ATTORNEYS GENERAL LEAD CASE: 16-AG-27240 CASES ____________________________________ THIS DOCUMENT RELATES TO: ALL STATE ATTORNEYS GENERAL ACTIONS November __, 2017 ____________________________________ THE STATE OF CONNECTICUT; THE STATE OF ALABAMA; PLAINTIFF STATES' [PROPOSED] THE STATE OF ALASKA; CONSOLIDATED AMENDED THE STATE OF ARIZONA; COMPLAINT THE STATE OF ARKANSAS; THE STATE OF CALIFORNIA; THE STATE OF COLORADO; THE DISTRICT OF COLUMBIA; THE STATE OF DELAWARE; Public Version THE STATE OF FLORIDA; THE STATE OF HAWAII; THE STATE OF IDAHO; THE STATE OF ILLINOIS; THE STATE OF INDIANA; THE STATE OF IOWA; THE STATE OF KANSAS; THE COMMONWEALTH OF KENTUCKY; THE STATE OF LOUISIANA; THE STATE OF MAINE; THE STATE OF MARYLAND; THE COMMONWEALTH OF MASSACHUSETTS; THE STATE OF MICHIGAN; THE STATE OF MINNESOTA; THE STATE OF MISSISSIPPI; THE STATE OF MISSOURI; THE STATE OF MONTANA; THE STATE OF NEBRASKA; THE STATE OF NEVADA; Case 2:17-cv-03768-CMR Document 3-1 Filed 10/31/17 Page 2 of 243 THE STATE OF NEW HAMPSHIRE; THE STATE OF NEW JERSEY; THE STATE OF NEW MEXICO; THE STATE OF NEW YORK; THE STATE OF NORTH CAROLINA; THE STATE OF NORTH DAKOTA; THE STATE OF OHIO; THE STATE OF OKLAHOMA; THE STATE OF OREGON; THE COMMONWEALTH OF PENNSYLVANIA; THE COMMONWEALTH OF PUERTO RICO; THE STATE OF SOUTH CAROLINA; THE STATE OF TENNESSEE; THE STATE OF UTAH; THE STATE OF VERMONT; THE COMMONWEALTH OF VIRGINIA; THE STATE OF WASHINGTON; THE STATE OF WEST VIRGINIA; THE STATE OF WISCONSIN; v. -
Belgian Veterinary Surveillance of Antibacterial Consumption National
Belgian Veterinary Surveillance of Antibacterial Consumption National consumption report 2020 Publication : 22 June 2021 1 SUMMARY This annual BelVet-SAC report is now published for the 12th time and describes the antimicrobial use (AMU) in animals in Belgium in 2020 and the evolution since 2011. For the third year this report combines sales data (collected at the level of the wholesalers-distributors and the compound feed producers) and usage data (collected at farm level). This allows to dig deeper into AMU at species and farm level in Belgium. With a consumption of 87,6 mg antibacterial compounds/kg biomass an increase of +0.2% is seen in 2020 in comparison to 2019. The increase seen in 2020 is spread over both pharmaceuticals (+0.2%) and antibacterial premixes (+4.0%). This unfortunately marks the end of a successful reduction in antibacterial product sales that was seen over the last 6 years resulting in a cumulative reduction of -40,2% since 2011. The gap seen in the coverage of the sales data with the Sanitel-Med collected usage data increased substantially compared to 2019, meaning continuous efforts need to be taken to ensure completeness of the collected usage data. When looking at the evolution in the number of treatment days (BD100) at the species level, as calculated from the SANITEL- MED use data, use increased in poultry (+5,0%) and veal calves (+1,9%), while it decreased in pigs (-3,1%). However, the numerator data for this indicator remain to be updated for 2020, potentially influencing the reliability of the result. -
(ESVAC) Web-Based Sales and Animal Population
16 July 2019 EMA/210691/2015-Rev.2 Veterinary Medicines Division European Surveillance of Veterinary Antimicrobial Consumption (ESVAC) Sales Data and Animal Population Data Collection Protocol (version 3) Superseded by a new version Superseded Official address Domenico Scarlattilaan 6 ● 1083 HS Amsterdam ● The Netherlands Address for visits and deliveries Refer to www.ema.europa.eu/how-to-find-us Send us a question Go to www.ema.europa.eu/contact Telephone +31 (0)88 781 6000 An agency of the European Union © European Medicines Agency, 2021. Reproduction is authorised provided the source is acknowledged. Table of content 1. Introduction ....................................................................................................................... 3 1.1. Terms of reference ........................................................................................................... 3 1.2. Approach ........................................................................................................................ 3 1.3. Target groups of the protocol and templates ......................................................................... 4 1.4. Organization of the ESVAC project ...................................................................................... 4 1.5. Web based delivery of data ................................................................................................ 5 2. ESVAC sales data ............................................................................................................... 5 2.1. -
APO-Roxithromycin Roxithromycin Consumer Medicine Information
APO-Roxithromycin Roxithromycin Consumer Medicine Information For a copy of a large print leaflet, Ph: 1800 195 055 What is in this leaflet · acute pharyngitis (sore throat and Before you take it discomfort when swallowing) This leaflet answers some common · tonsillitis When you must not take it questions about roxithromycin. It · sinusitis does not contain all the available Do not take this medicine if you information. It does not take the · acute bronchitis (infection of the have an allergy to: bronchi causing coughing) place of talking to your doctor or · roxithromycin pharmacist. · worsening of chronic bronchitis · any other macrolide antibiotics All medicines have risks and · pneumonia (lung infection (e.g. azithromycin, clarithromycin benefits. Your doctor has weighed characterised by fever, malaise, or erythromycin) the risks of you using this medicine headache) · any of the ingredients listed at the against the benefits they expect it · skin and soft tissue infections end of this leaflet will have for you. · non gonococcal urethritis Some of the symptoms of an allergic Ask your doctor or pharmacist: · impetigo (bacterial infection reaction may include: · if there is anything you do not causing sores on the skin) · shortness of breath understand in this leaflet, · wheezing or difficulty breathing · if you are worried about taking How it works your medicine, or · swelling of the face, lips, tongue, Roxithromycin is an antibiotic that throat or other parts of the body · to obtain the most up-to-date belongs to a group of medicines · rash, itching or hives on the skin information. called macrolides. You can also download the most up These antibiotics work by killing or Do not take this medicine if you to date leaflet from stopping the growth of the bacteria have severe liver problems. -
Third ESVAC Report
Sales of veterinary antimicrobial agents in 25 EU/EEA countries in 2011 Third ESVAC report An agency of the European Union The mission of the European Medicines Agency is to foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health. Legal role Guiding principles The European Medicines Agency is the European Union • We are strongly committed to public and animal (EU) body responsible for coordinating the existing health. scientific resources put at its disposal by Member States • We make independent recommendations based on for the evaluation, supervision and pharmacovigilance scientific evidence, using state-of-the-art knowledge of medicinal products. and expertise in our field. • We support research and innovation to stimulate the The Agency provides the Member States and the development of better medicines. institutions of the EU the best-possible scientific advice on any question relating to the evaluation of the quality, • We value the contribution of our partners and stake- safety and efficacy of medicinal products for human or holders to our work. veterinary use referred to it in accordance with the • We assure continual improvement of our processes provisions of EU legislation relating to medicinal prod- and procedures, in accordance with recognised quality ucts. standards. • We adhere to high standards of professional and Principal activities personal integrity. Working with the Member States and the European • We communicate in an open, transparent manner Commission as partners in a European medicines with all of our partners, stakeholders and colleagues. network, the European Medicines Agency: • We promote the well-being, motivation and ongoing professional development of every member of the • provides independent, science-based recommenda- Agency. -
Danmap 2006.Pmd
DANMAP 2006 DANMAP 2006 DANMAP 2006 - Use of antimicrobial agents and occurrence of antimicrobial resistance in bacteria from food animals, foods and humans in Denmark Statens Serum Institut Danish Veterinary and Food Administration Danish Medicines Agency National Veterinary Institute, Technical University of Denmark National Food Institute, Technical University of Denmark Editors: Hanne-Dorthe Emborg Danish Zoonosis Centre National Food Institute, Technical University of Denmark Mørkhøj Bygade 19 Contents DK - 2860 Søborg Anette M. Hammerum National Center for Antimicrobials and Contributors to the 2006 Infection Control DANMAP Report 4 Statens Serum Institut Artillerivej 5 DK - 2300 Copenhagen Introduction 6 DANMAP board: National Food Institute, Acknowledgements 6 Technical University of Denmark: Ole E. Heuer Frank Aarestrup List of abbreviations 7 National Veterinary Institute, Tecnical University of Denmark: Sammendrag 9 Flemming Bager Danish Veterinary and Food Administration: Summary 12 Justin C. Ajufo Annette Cleveland Nielsen Statens Serum Institut: Demographic data 15 Dominique L. Monnet Niels Frimodt-Møller Anette M. Hammerum Antimicrobial consumption 17 Danish Medicines Agency: Consumption in animals 17 Jan Poulsen Consumption in humans 24 Layout: Susanne Carlsson Danish Zoonosis Centre Resistance in zoonotic bacteria 33 Printing: Schultz Grafisk A/S DANMAP 2006 - September 2007 Salmonella 33 ISSN 1600-2032 Campylobacter 43 Text and tables may be cited and reprinted only with reference to this report. Resistance in indicator bacteria 47 Reprints can be ordered from: Enterococci 47 National Food Institute Escherichia coli 58 Danish Zoonosis Centre Tecnical University of Denmark Mørkhøj Bygade 19 DK - 2860 Søborg Resistance in bacteria from Phone: +45 7234 - 7084 diagnostic submissions 65 Fax: +45 7234 - 7028 E. -
Intracellular Penetration and Effects of Antibiotics On
antibiotics Review Intracellular Penetration and Effects of Antibiotics on Staphylococcus aureus Inside Human Neutrophils: A Comprehensive Review Suzanne Bongers 1 , Pien Hellebrekers 1,2 , Luke P.H. Leenen 1, Leo Koenderman 2,3 and Falco Hietbrink 1,* 1 Department of Surgery, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands; [email protected] (S.B.); [email protected] (P.H.); [email protected] (L.P.H.L.) 2 Laboratory of Translational Immunology, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands; [email protected] 3 Department of Pulmonology, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands * Correspondence: [email protected] Received: 6 April 2019; Accepted: 2 May 2019; Published: 4 May 2019 Abstract: Neutrophils are important assets in defense against invading bacteria like staphylococci. However, (dysfunctioning) neutrophils can also serve as reservoir for pathogens that are able to survive inside the cellular environment. Staphylococcus aureus is a notorious facultative intracellular pathogen. Most vulnerable for neutrophil dysfunction and intracellular infection are immune-deficient patients or, as has recently been described, severely injured patients. These dysfunctional neutrophils can become hide-out spots or “Trojan horses” for S. aureus. This location offers protection to bacteria from most antibiotics and allows transportation of bacteria throughout the body inside moving neutrophils. When neutrophils die, these bacteria are released at different locations. In this review, we therefore focus on the capacity of several groups of antibiotics to enter human neutrophils, kill intracellular S. aureus and affect neutrophil function. We provide an overview of intracellular capacity of available antibiotics to aid in clinical decision making. -
Paromomycin Intramuscular Injection Safe, Effective, and Affordable Treatment for Visceral Leishmaniasis
Paromomycin Intramuscular Injection Safe, effective, and affordable treatment for visceral leishmaniasis Visceral leishmaniasis (VL), or kala-azar, is a neglected and deadly infectious disease that is transmitted through the bite of a sand fly. It affects the visceral organs, causing chronic fever, weight loss, and anemia. If left untreated, VL is nearly always fatal, especially in children. VL is endemic in 79 countries, PMIM REGISTRATION STATUS primarily in the developing world. The population at risk is estimated at 200 million; 20,000 to 40,000 people are believed to die from VL each year. Until PMIM is registered with the recently, the only available therapies were expensive for the most vulnerable, National Drug Development poor populations—from US$20 to $250—and could be toxic or ineffective. agencies of India (2006), Nepal (2012), and Uganda (2012). Paromomycin, an off-patent aminoglycoside antibiotic, is an established drug PMIM is included on the Essential with an extensive history of use and a well-characterized safety profile. Medicine Lists of the World Health OneWorld Health (OWH), a nonprofit drug development program dedicated to Organization (2007), Bangladesh, discovering and advancing lifesaving medicines for neglected diseases, Ethiopia, India, Nepal, Sudan, and developed paromomycin intramuscular injection (PMIM) as an effective, Uganda. inexpensive, and safe treatment for VL and worked with leading clinical researchers and the Indian pharmaceutical company Gland Pharma to Registration for PMIM is ongoing in manufacture and distribute the treatment. The cost of a course of treatment Bangladesh, Ethiopia, Kenya, and with PMIM is less than US$20, significantly lower than other currently Sudan. -
Paromomycin General Information Operating Range
Paromomycin General Information Elemental formula: C23H45N5O14 Molecular weight: 615,23 g/mol Material class: Aminoglycoside CAS Registry Number: 7542-37-2 Operating range The active ingredient Paromomycin is a natural antibiotic that is extensively used in pharmaceutical industry. It acts as a prophylaxis and treatment agent of the hepatic encephalopathy, amoebic dysentery and is also used for präoperative reduction of ammonia forming intestine flora. According to the World Health Organization [1] it will also be applied to fight various parasitic diseases and is among to the most essential medicines at the present time. Studies from institute of OneWorld Health suggest that particularly in tropical areas ectoparasitically transmitted protozoan pathogens of leishmaniasis can be effectively medicated by this agent via intramuscular injection. This treatment, as a clinical study in India shows, is not less effective than the reference preparation Amphotericin B. Parallel to the recently completed approval process in India as well as the status of an orphan drug in the United States and Europe, there are additional clinical test phases for visceral leishmaniasis (black fever) in Africa [2]. The first time effectiveness from Paromomycin against cutaneous leishmaniasis were found in 1960s in the USSR [3]. History / Evolutionary origin Paromomycin was isolated first from Streptomyces krestomuceticus in the 1950s and introduced as Humatin by the pharmaceutical company Parke-Davis (now Pfizer) since the 1960s [4]. At hepatic encephalopathy this preparation is used. The disease causes brain damage as a result of liver dysfunction, by in the urea cycle insufficient metabolized ammonia. Paromomycin as Humatin capsules reduces the ammonia- producing bacteria in the intestine and thus ensures improved symptoms. -
Needs and Challenges in Developing a New Treatment for Visceral Leishmaniasis
Needs and Challenges in Developing a New Treatment for Visceral Leishmaniasis Shyam Sundar, MD Professor of Medicine Institute of Medical Sciences Banaras Hindu University, India TREATMENT OF VISCERAL LEISHMANIASIS Efficacy of SSG 20mg/kg/d in Bihar, India during 1988-2002. 100 80 60 40 20 0 1988 1990 1992 1994 1996 1998 2000 2002 Sundar & Olliaro Amphotericin B • Polyene antibiotic (Amphotericin B deoxycholate) • Dose 0.75-1.0 mg daily or alternate days for 15-20 infusions • Expensive & needs hospitalisation for 4-5 weeks • Infusion reactions, thrombophlebitis common • Hypokalemia, myocarditis & death are serious, but uncommon, toxicities • High Cure rates ~100% • Used as first line drug in Bihar with areas of Sb resistance Single Dose Liposomal Amphotericin B (AmBisome) in Indian Kala-azar Total Dose No. of Treat. Cure Rate mg/kg Patients Dur. 5 46 1 91 ( Sundar, BMJ,2002)* 5 45 5 93 7.5 203* 1 90 (Sundar, CID, 2003)* 15 17 1 100 (Thakur, AAC, 2001) * Multicenter Liposomal Amphotericin B - AmBisome • Total dose – most important determinant in the outcome – Total dose requirement • 20-24 mg/kg - for Brazil and Europe • 18-20 mg/kg – for Africa • 15 mg/kg – for Asia • 40 mg/kg for Immunosuppressed • Even after a remarkable 90% decrease in the price of AmBisome, access remains a problem • Problem of cold chain Paramomycin (Aminosidine) • An aminoglycoside (parenteral) • Good antileishmanial activity, earlier used for bacterial & Parasitic infections • In several phase II studies 16 mg/kg for 3 weeks cured 93% VL patients • Has been licensed