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Adverse Event Reporting System
Results: 638

#	Item
181	FDAs MedWatch Program: Voluntarily Reporting Problems to the FDA Add to Reading List Source URL: www.fda.gov. Language: English MedWatch Health Office of Regulatory Affairs Center for Drug Evaluation and Research Center for Veterinary Medicine Adverse Event Reporting System Adverse effect Food and Drug Administration Pharmaceutical sciences Clinical research
182	Pregnancy Registries: Data collection/experience with vaccines Adel Abou-Ali, PharmD, ScD, MS Deputy Director of Global Pharmacoepidemiology & Risk Management Add to Reading List Source URL: www.fda.gov Language: English Drug safety Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Pregnancy Miscarriage DPT vaccine Medicine Health Vaccines
183	FOOD AND DRUG ADMINISTRATION Add to Reading List Source URL: www.fda.gov Language: English - Date: 2008-05-02 08:31:29 Pharmaceutical sciences Organic chemistry Pharmacology Anilides Fentanyl Cephalon Center for Drug Evaluation and Research Actiq Adverse Event Reporting System Food and Drug Administration Piperidines Chemistry
184	Consumer Health Information www.fda.gov/consumer FDA and ISMP Work to Prevent Medication Errors Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Patient safety Pharmacology Adverse Event Reporting System Pharmaceutical industry Medical error MedWatch Pharmacy FDA Consumer Medicine Food and Drug Administration Health
185	January 9, 2013 — Data from 2012 Quarter 2 PERSPECTIVES IN THIS ISSUE Finasteride (PROPECIA, PROSCAR) and possibly persistent sexual side effects Methylphenidate patch (DAYTRANA) and product problems Update on anticoa Add to Reading List Source URL: www.ismp.org Language: English - Date: 2013-01-09 09:00:07 Pharmacology Lactams Clinical research Pharmaceutical industry Finasteride Attention-deficit hyperactivity disorder Adverse Event Reporting System Dutasteride Methylphenidate Chemistry Medicine Organic chemistry
186	VACCINE SAFETY Information for Parents ENGLISH: CDC National Immunization Information HOT LINE Add to Reading List Source URL: www.state.in.us Language: English - Date: 2014-11-14 18:24:45 Biology Drug safety Microbiology Mononegavirales Pediatrics Vaccine injury Vaccine Adverse Event Reporting System Vaccine Vaccination Medicine Health Vaccines
187	What Is VAERS? vaccine. Rarely, people who have been vaccinated will get unexpected reactions that are serious and should be reported to VAERS. Add to Reading List Source URL: www.state.in.us Language: English - Date: 2014-11-14 18:24:46 Vaccines Medicine Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Vaccine injury Anthrax vaccines Safety Drug safety Prevention
188	CONFIDENTIAL “Safety Reporting Requirements for Human Drug and Biological Products” (TOME) Eli Lilly and Company has reviewed the titled draft regulation and is submitting the following comments, questions and recom Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:03:35 Health Food and Drug Administration Clinical research Pharmaceutical industry Drug safety MedDRA Adverse event Vaccine Adverse Event Reporting System MedWatch Pharmacology Pharmaceutical sciences Medicine
189	Baxter Healthcare Comments to the Proposed Safety Reporting Requirements for Human Drug and Biological Products: Proposed Rules October 14, 2003 Section FR Page Number Comment[removed]c)(2)(v)(C) (vi) & (vii) 12474 The r Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:03:40 Clinical research Research Pharmaceutical industry Clinical pharmacology United States Public Health Service MedDRA MedWatch Adverse event Adverse Event Reporting System Pharmacology Pharmaceutical sciences Food and Drug Administration
190	This graph depicts what happens to an adverse event report that is submitted to FDA. First, FDA may receive one of two types of reports: mandatory or voluntary. A mandatory report is sent to FDA by a manufacturer, import Add to Reading List Source URL: www.fda.gov. Language: English Food and Drug Administration Clinical research Pharmaceutical industry Therapeutics Adverse event Adverse Event Reporting System Unique Device Identification Pharmaceutical sciences Pharmacology Research

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