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Adverse event
Results: 2359

#	Item
831	Department of Health and Human Services Pediatric Postmarketing Adverse Event Review Add to Reading List Source URL: www.fda.gov Language: English Organochlorides Stimulants Nootropics Pharmacology Attention-deficit hyperactivity disorder Methylphenidate Sertraline Lamotrigine Attention deficit hyperactivity disorder Chemistry Medicine Organic chemistry
832	Food and Drug Administration Regulations; Drug and Biological Product Consolidation; Addresses; Technical Amendment; Final Rule Add to Reading List Source URL: www.fda.gov. Language: English Biotechnology Center for Biologics Evaluation and Research Center for Drug Evaluation and Research Adverse Event Reporting System Biologic New Drug Application Animal drugs Title 21 of the Code of Federal Regulations Code of Federal Regulations Food and Drug Administration Medicine Health
833	CDER Clinical Review Template Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical sciences Pharmaceutical industry Design of experiments Epidemiology Botulinum toxin Clinical trial Botulism Serious adverse event Pharmacology Medicine Health
834	This document is scheduled to be published in the Federal Register on[removed]and available online at http://federalregister.gov/a[removed], and on FDsys.gov[removed]P DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: s3.amazonaws.com Language: English - Date: 2014-07-17 08:54:28 Safety Vaccine Adverse Event Reporting System Center for Biologics Evaluation and Research Adverse Event Reporting System Food and Drug Administration Medicine Health
835	Department of Health and Human Services Public Health Service Food and Drug Administration Center for Drug Evaluation and Research Office of Surveillance and Epidemiology Add to Reading List Source URL: www.fda.gov Language: English Adverse Event Reporting System Rheumatoid arthritis Health Medicine Immunosuppressants Tocilizumab Anatomy
836	MEMORANDUM DEPARTMENT OF HEALTH AND HUMAN SERVICES PUBLIC HEALTH SERVICE FOOD AND DRUG ADMINISTRATION CENTER FOR DRUG EVALUATION AND RESEARCH Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-11-13 08:05:23 Ketones Ondansetron 5-HT3 antagonist Adverse Event Reporting System Chemistry Pharmacology Medicine Antiemetics GlaxoSmithKline Imidazoles
837	U.S. Department of Health and Human Services Food and Drug Administration Center for Food Safety and Applied Nutrition CFSAN Adverse Event Reporting System Voluntary and Mandatory Reports on 5-Hour Energy, Monster Energy Add to Reading List Source URL: www.fda.gov. Language: English Food and Drug Administration Research Medicine Pharmacology Adverse event Serious adverse event MedWatch Canadian Anti-racism Education and Research Society Energy drink Clinical research Pharmaceutical industry Pharmaceutical sciences
838	Microsoft Word - Insert1_Letter Poster FA309-05 Final v2_v1.doc Add to Reading List Source URL: www.hospira.com Language: English - Date: 2014-10-28 03:45:34 Research MedWatch Clinical research Hospira Pharmaceutical industry Adverse event Pharmaceutical sciences Food and Drug Administration Pharmacology
839	FDA PERSPECTIVE ON OPPORTUNITIES FOR PAS IMPLEMENTATION Veronica Sansing, PhD, MS US Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Pharmacology Adverse event Food and Drug Administration Clinical research Research Pharmaceutical sciences
840	BLA EFFICACY SUPPLEMENT MEDICAL FINAL REVIEW MEMO OF SPONSOR’S RESPONSE TO COMPLETE REVIEW LETTER Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical sciences Clinical research Pharmaceutical industry Food and Drug Administration Adverse event Adverse effect Clinical trial Center for Biologics Evaluation and Research Pharmacology Medicine Health

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