medication misbranding

Medication misbranding occurs when a drug's packaging, labeling, or information is incorrect, misleading, or lacks proper details, which can cause confusion or improper use. This may include wrong instructions, incorrect expiration dates, or missing safety warnings. Misbranding can happen intentionally or unintentionally and poses risks to patient safety, as it can lead to incorrect dosing or use of the medication. Regulatory agencies require accurate labeling to ensure medicines are used safely and effectively. Proper labeling helps healthcare providers and patients understand how to correctly administer and handle medications, reducing the risk of errors and adverse effects.