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Adverse Event Reporting System
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161	Microsoft Word - PDUFA IV Annual IT Assessment _FY2010_.doc Add to Reading List Source URL: www.fda.gov Language: English Health Clinical research Pharmaceuticals policy Prescription Drug User Fee Act Medical informatics Drug safety Regulated Product Submissions Center for Biologics Evaluation and Research Adverse Event Reporting System Food and Drug Administration Medicine Research
162	Department of Health and Human Services Public Health Service Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Birth control Cyclopropanes Enantiopure drugs Drospirenone Medicine Pharmaceutical sciences Adverse Event Reporting System Bayer HealthCare Pharmaceuticals Combined oral contraceptive pill Pharmacology Hormonal contraception Beyaz
163	What Types of Events Should I Report? You should report any adverse event that happens after getting a vaccine, even if you are not sure that the vaccine caused the adverse event. It is especially important to report any Add to Reading List Source URL: www.fda.gov. Language: English Health Vaccine Adverse Event Reporting System Vaccine injury Adverse effect Vaccine Vaccination schedule Vaccination National Childhood Vaccine Injury Act Anthrax vaccines Drug safety Safety Medicine
164	Consumer Health Information www.fda.gov/consumer WANTED: Consumers to Report Problems H Add to Reading List Source URL: www.fda.gov. Language: English MedWatch Clinical research Medicinal chemistry FDA Consumer Adverse Event Reporting System Package insert Food and Drug Administration Pharmacology Pharmaceutical sciences
165	H:kFile1ject Work FileshangeESRR FilescinesRegionalMegaInstanceUpdate.xml Add to Reading List Source URL: www.fda.gov Language: English Hematology Embolism Pulmonary embolism Heart failure Medical prescription Vaccine Adverse Event Reporting System Autopsy Medicine Health Medical emergencies
166	Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Dextromethorphan Center for Drug Evaluation and Research Adverse Event Reporting System Consumer Healthcare Products Association Cough medicine Over-the-counter drug Pharmacology Medicine Food and Drug Administration
167	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 Medical physics Radiopharmaceuticals Radiobiology Food and Drug Administration Adverse Event Reporting System Technetium (99mTc) sestamibi Adverse effect Technetium-99m Pharmacovigilance Medicine Health Pharmacology
168	CONTENTS EXECUTIVE SUMMARY ............................................................................................................. 2 1 BACKGROUND ................................................................... Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Abatacept Rheumatoid arthritis Adverse Event Reporting System Adalimumab Uveitis Juvenile idiopathic arthritis Rituximab Co-stimulation Medicine Immunosuppressants Health
169	Understanding the Vaccine Adverse Event Reporting System (VAERS) Add to Reading List Source URL: www.fda.gov. Language: English Vaccines Prevention Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Vaccine injury Anthrax vaccines Medicine Safety Drug safety
170	Guidance for Industry: How to Complete the Vaccine Adverse Events Reporting System Form (VAERS-1) Add to Reading List Source URL: www.fda.gov. Language: English Drug safety Food and Drug Administration Pharmacology Vaccines Vaccination Vaccine Adverse Event Reporting System Vaccine injury Adverse effect National Childhood Vaccine Injury Act Medicine Health Safety

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