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1. www.fda.gov › drugs › drug-approvals-and-databasesFDA Adverse Event Reporting System (FAERS) Database

   www.fda.gov › drugs › drug-approvals-and-databases

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   We are in the process of updating FDA.gov content to reflect these changes. FDA Adverse Event Reporting System Database supports the FDA's post-marketing safety surveillance...

   • MedWatch

     MedWatch receives reports from the public and when...

2. www.fda.gov › drugs › questions-and-answers-fdas-adverse-event-reporting-systemFDA Adverse Event Reporting System (FAERS) Public Dashboard

   www.fda.gov › drugs › questions-and-answers-fdas-adverse-event-reporting-system

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   7 gru 2023 · The intention of this tool is to expand access of FAERS data to the general public to search for information related to human adverse events reported to the FDA by the pharmaceutical...

3. www.fda.gov › safety › medwatchMedWatch: FDA Safety Information & Adverse Event Reporting...

   www.fda.gov › safety › medwatch

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   MedWatch receives reports from the public and when appropriate, publishes safety alerts for FDA-regulated products such as: Biologics such as blood components, blood/plasma derivatives and...

4. www.fda.gov › medical-devices › medical-device-safetyMedical Device Reporting (MDR): How to Report Medical Device...

   www.fda.gov › medical-devices › medical-device-safety

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   27 lip 2023 · Medical Device Reporting (MDR) is one of the postmarket surveillance tools the FDA uses to monitor device performance, detect potential device-related safety issues, and contribute to...

5. fis.fda.gov › extensions › FPD-FAQFAERS Public Dashboard - FAQ - Food and Drug Administration

   fis.fda.gov › extensions › FPD-FAQ

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   The FDA Adverse Event Reporting System (FAERS) is a database that contains adverse event reports, medication error reports and product quality complaints resulting in adverse events that were...

6. fis.fda.gov › extensions › fpdwidgetsFAERS Public Dashboard - About - Food and Drug Administration

   fis.fda.gov › extensions › fpdwidgets

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   The FDA Adverse Event Reporting System (FAERS) is a database that contains adverse event reports, medication error reports and product quality complaints resulting in adverse events that were...

7. open.fda.gov › data › faersFDA Adverse Event Reporting System

   open.fda.gov › data › faers

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   The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to support...