Patient safety

Report a side effect

If something feels off, tell us. A licensed clinician on the Kindr Health team reviews every report — usually within one business day — and can coordinate with the pharmacy that filled your medication and help you file an FDA MedWatch report if it meets the criteria. You do not need an account. Anonymous reports are welcome.

If this is an emergency — call 911 or go to the nearest emergency room. Do not wait for a response to this form. You can also reach us at +1 (844) 74-KINDR.

Contact info is optional. Leave it blank to report anonymously — a clinician can still review it, but we won't be able to follow up.

Your name (optional)

Email (optional)

Medication or product *Dose you were taking

Started medication

Symptom onset

Symptoms are still happeningHow severe is it? *Did any of these happen? (check all that apply)

Hospitalization Life-threatening event Disability / permanent damage Emergency room visit Required medical intervention Birth defect Death

Describe what you experienced *Other medications, supplements, or peptides you takeRelevant medical history (optional)

Age

Sex

Weight (lb)

What happens next: After you submit, we'll show you a one-click link to file the same report with the FDA MedWatch program. Reporting to the FDA is voluntary but helps regulators catch safety signals across the entire US drug supply.

How Kindr handles reports

Every report is triaged by the Kindr Health Clinical Team within one business day.
Severe or life-threatening reports are escalated immediately to the prescribing clinician.
When the medication was fulfilled by a partner pharmacy (e.g. Arora Health, VialsRX), we route the report to their pharmacovigilance contact.
We help you file with FDA MedWatch — the national adverse-event system that feeds FAERS.
Aggregate, de-identified signals are reviewed monthly by our Medical Advisory Board.