Comprehensive and Detailed Step-by-Step Explanation:
MedWatchis theFDA's Safety Information and Adverse Event Reporting Program, used totrack drug and device safety concerns.Pharmacists and healthcare professionals should report:
Adverse drug reactions (ADRs).
Medical device failures or malfunctions.
Medication errors that lead to harm.
Product quality issues related to safety.
????Explanation of Answer Choices:✅D. Medical device malfunctions→Correct.MedWatch monitors medical device safety, including pacemakers, insulin pumps, and inhalers.❌A. Medication reimbursement complaints→ Incorrect.Billing and insurance issues are not handled by MedWatch.❌B. Damaged medications received from a wholesaler→ Incorrect.These issues should be reported to the wholesaler or manufacturer, not MedWatch.❌C. Complaints about pharmacy staff→ Incorrect.These concerns should be reported to the state board of pharmacy.
????Reference:
FDA MedWatch Program
PTCB Exam: Medication Safety & Reporting
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