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Adverse Event Reporting System
Results: 638

#	Item
271	MedWatch: Communicating and Educating the Public April 30, 2013 Anna M. Fine, PharmD, MS Heidi C. Marchand, PharmD Add to Reading List Source URL: www.fda.gov Language: English Pharmacology MedWatch Pharmaceutical sciences Clinical research Pharmaceutical industry Medical terms Adverse Event Reporting System Medicine Food and Drug Administration Health
272	Department of Health and Human Services Public Health Service Food and Drug Administration Center for Biologics Evaluation and Research Office of Biostatistics and Epidemiology Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmacology Clinical research Pharmaceutical industry United States Public Health Service Center for Biologics Evaluation and Research Clinical trial Adverse Event Reporting System Food and Drug Administration Pharmaceutical sciences Health
273	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 Fixed dose combination Lopinavir/ritonavir Lopinavir Organic chemistry Drug safety Adverse Event Reporting System Antiretroviral drug Pharmacovigilance Protease inhibitors Chemistry Pharmacology
274	26-P_XXX-MedEffect Canada Chart Description_e_02.indd Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-06-24 11:52:43 Patient safety Medical terms Clinical research Adverse effect Drug safety Postmarketing surveillance Adverse Event Reporting System Patient safety organization Medicine Health Pharmacology
275	Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Antitussives Dissociative drugs Dextromethorphan Morphinans Adverse Event Reporting System Center for Drug Evaluation and Research Cough medicine Recreational use of dextromethorphan Pharmacology Neurochemistry Medicine
276	MedWatch Practice Portal Norman S. Marks, MD, MHA Office of Health and Constituent Affairs 1 Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research MedWatch Postmarketing surveillance Adverse Event Reporting System Adverse effect Pharmacology Food and Drug Administration Pharmaceutical sciences
277	Working Group Draft Report – April 14, 2009 For Public Comment NVAC Vaccine Safety Working Group Draft Report April 14, 2009 Add to Reading List Source URL: archive.hhs.gov Language: English - Date: 2009-04-16 11:26:54 Safety Drug safety Public safety Vaccines Vaccination Vaccine Safety Datalink Vaccine Adverse Event Reporting System National Center for Immunization and Respiratory Diseases Vaccine Centers for Disease Control and Prevention Prevention Medicine
278	Bio-Ontologies Submission Template Add to Reading List Source URL: www2.unb.ca Language: English - Date: 2013-06-27 08:38:08 Health Ontology Drug safety Influenza vaccine Vaccine Adverse Event Reporting System Adverse effect OBO Foundry Meningococcal vaccine Vaccine Vaccines Medicine Vaccination
279	Comments of Consumers Union before the Food and Drug Administration Science Board April 15, 2005 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-04-20 16:08:01 Health Food and Drug Administration COX-2 inhibitors Pharmaceutical industry Pharmacy Rofecoxib Adverse Event Reporting System Pharmacovigilance Clinical trial Pharmacology Pharmaceutical sciences Medicine
280	DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration Rockville, MD[removed]DATE: Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-02-11 16:14:03 Oncology Lymphoma Type 1 hypersensitivity Pimecrolimus Tacrolimus Calcineurin Atopy Atopic dermatitis Adverse Event Reporting System Medicine Immunosuppressants Macrolides

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