Tag: FDA patient reporting
How to File a Direct Complaint with the FDA as a Patient
Learn how patients can file direct complaints with the FDA about adverse reactions, product failures, or safety issues with drugs, devices, and supplements. Step-by-step guide on using MedWatch and the Safety Reporting Portal.
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Contamination controls in generic drug manufacturing prevent harmful residues and microbes from entering medicines. Learn how cleanrooms, real-time monitoring, and human factors impact drug safety-and what’s changing by 2025.
Published ON: 11 DecThe first generic drug company to file a patent challenge gets 180 days of exclusive sales rights. But this rule, meant to lower drug prices, is often manipulated-delaying competition and keeping patients from affordable medicines.
Published ON: 15 DecPeptic ulcer disease is caused mainly by H. pylori bacteria or NSAIDs. Learn how antibiotics and acid-reducing medications like PPIs work together to heal ulcers, what to expect during treatment, and how to avoid relapse.
Published ON: 23 DecLearn how patients can file direct complaints with the FDA about adverse reactions, product failures, or safety issues with drugs, devices, and supplements. Step-by-step guide on using MedWatch and the Safety Reporting Portal.
Published ON: 25 DecLearn the essential documentation requirements for recording generic drug substitutions in pharmacy practice. Understand state laws, what to log, common mistakes, and how to avoid errors that impact patient safety.
Published ON: 1 Dec