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FDA Adverse Event Reporting System Database supports the FDA's post-marketing safety surveillance program for all marketed drug and therapeutic biologic products. It contains adverse...
- MedWatch
MedWatch receives reports from the public and when...
- MedWatch
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...
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...
21 wrz 2023 · Mobile App: Download the Yellow Card app from the App Store or Google Play. Now Paient App: You can report side effects conveniently from the nowpatient.com App Paper forms: Available from the MHRA or in the back of the British National Formulary (BNF).
The FDA hopes to harness the power of the public in better monitoring adverse events associated with medical devices, drugs and vaccines through its newly released MedWatcher mobile app.
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...
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...