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Adverse Event Reporting System
Results: 638

#	Item
561	Implementation Guide forImmunization Data Transactions using HL7 v2.3.1 (June 2006) Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2012-05-16 11:34:23 Nursing informatics Centers for Disease Control and Prevention International standards Standards organizations Health Level 7 LOINC Immunization registry Vaccine Adverse Event Reporting System Immunization Health Medicine Medical informatics
562	External Peer Review of the Clinical Immunization Safety Assessment (CISA) Network Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2011-07-05 08:31:13 Medicine Drug safety Public safety Vaccination Vaccines Vaccine Adverse Event Reporting System Vaccine Safety Datalink Vaccine Centers for Disease Control and Prevention Prevention Safety
563	FDA Notifying Health Care Providers about the Risks of Purchasing Unapproved Injectable Cancer Medications from Unlicensed Sources Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Office of Criminal Investigations Center for Drug Evaluation and Research Federal Food Drug and Cosmetic Act Online pharmacy Adverse Event Reporting System Food and Drug Administration Health Medicine
564	Ensuring the Safety of Vaccines in the United States Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2013-04-09 08:29:39 Prevention Drug safety Centers for Disease Control and Prevention Public safety Virology Vaccine Adverse Event Reporting System Rotavirus vaccine Vaccine Safety Datalink Vaccine Vaccines Medicine Vaccination
565	Guidance for Industry Safety Labeling Changes — Implementation of Section 505(o)(4) of the FD&C Act Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmacology Pharmaceutical industry Clinical research Federal Food Drug and Cosmetic Act New Drug Application Adverse Event Reporting System Over-the-counter drug Approved drug Food and Drug Administration Pharmaceuticals policy Pharmaceutical sciences
566	Guidance for Industry Providing Submissions in Electronic Format — Postmarketing Safety Reports DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Research Adverse Event Reporting System Structured Product Labeling Center for Biologics Evaluation and Research New Drug Application Postmarketing surveillance Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Health
567	Guidance for Industry Good Pharmacovigilance Practices and Pharmacoepidemiologic Assessment Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Food and Drug Administration Pharmaceuticals policy Clinical research Drug safety Adverse Event Reporting System Pharmacovigilance Center for Biologics Evaluation and Research Adverse event Pharmacology Medicine Health
568	EDIT _RIAL Pharmacovigilance in the 21st Century: New Systematic Tools for an Old Problem Ana Szarfman, M.D., Ph.D., Joseph M. Tonning, M.D., M.P.H., and P. Murali Doraiswamy, M.D. The large number of adverse-event repor Add to Reading List Source URL: www.fda.gov Language: English Piperazines Food and Drug Administration Drug safety Clinical research Adverse Event Reporting System Pharmacovigilance Adverse effect MedWatch Valproic acid Pharmacology Medicine Pharmaceutical sciences
569	STRENGTHENING OUR NATIONAL SYSTEM FOR MEDICAL DEVICE POSTMARKET SURVEILLANCE UPDATE AND NEXT STEPS Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmacology Unique Device Identification Health informatics Clinical research Electronic health record Adverse event Adverse Event Reporting System Medical device Medicine Health Food and Drug Administration
570	Guidance for Industry Postmarketing Safety Reporting for Human Drug and Biological Products Including Vaccines DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Research Adverse Event Reporting System Center for Biologics Evaluation and Research Validation Regulatory requirement New Drug Application Biologic Center for Drug Evaluation and Research Postmarketing surveillance Food and Drug Administration Medicine Pharmaceutical sciences

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