What happens if I don't report an adverse event?

What happens if I don't report an adverse event?

Not reporting an adverse event can lead to serious consequences, including patient harm, regulatory penalties, and loss of trust.

Can you give me examples of adverse events that should be reported?

Sure! Examples include medication errors, allergic reactions, and unexpected side effects.

What are the legal implications of failing to report?

Failing to report can result in legal action against healthcare providers and institutions, including fines and lawsuits.

How can I report an adverse event?

You can report an adverse event through your healthcare provider, a regulatory agency, or directly to the manufacturer.

Is there a time limit for reporting adverse events?

Yes, many regulatory agencies have specific time frames for reporting, often within 24 to 72 hours of the event.