Reference

Side effects & reports

Three ways in: pick a peptide, describe what you're feeling, or file an adverse event report. Each entry shows severity, how common it is, what others did, and when to stop.

Pharmacovigilance · v1 preview

If something happened, the record matters.

You can file a report without an account, without an email, without identifying yourself. Reports are reviewed manually before they appear on the relevant product page. Clustering and automatic alerts arrive in v2.

Medical emergency? Stop — call your local emergency number first. This is a record, not a response system.

01 · Substance

02 · Product (optional)

Leave blank if not from a catalogued product.

03 · Batch number (optional)

From the vial label or COA, if available.

04 · Severity

Mild — noticeable, no intervention neededModerate — required dose change or OTC interventionSevere — required clinician contactSerious — hospitalisation, disability, life-threatening

05 · What happened

Plain language. Onset timing, duration, what you did. Avoid identifying details. Min 10 characters.

06 · Concomitant substances (optional)

07 · Contact (optional)

Email only used if a reviewer needs to clarify. Never published. Never required.

By submitting you agree the structured fields can be published under CC BY-SA 4.0 as part of the open dataset.