/ Registry / Adverse event
// ⚠ Report · structured · anonymous
Report an adverse event.
Even mild. Especially the ones you are not sure are related. Negative data is exactly what this field is starving for, and self-report systems systematically under-collect it.
// If this is an emergency
Call 911. Then read this.
Chest pain, difficulty breathing, facial or throat swelling, severe abdominal pain, fainting, or a rapidly spreading rash are emergencies. Get seen first. Report afterwards.
// Report right now
Two places, today.
- Your prescriber or physician. First call, always — they can act on it.
- FDA MedWatch. For anything serious, report it federally. It takes about ten minutes and it is the only channel that reaches a regulator. MedWatch reporting →
Reporting to the registry does not replace either of those. It sits alongside them.
// Registry intake
Structured AE form reopens shortly.
The structured, severity-graded AE form is moving onto its own IRB-governed system, separate from this website. killer.health itself holds no participant records. Leave your email and you get the link the day it opens.
// How severity is graded
MILD
Noticeable, tolerable, resolved without intervention. Injection-site redness, transient flush, mild fatigue.
MODERATE
Interfered with normal activity, or required an intervention. GI upset, persistent headache, sleep disruption.
SEVERE
Required medical attention, hospitalisation, or caused lasting harm. Report federally as well.
When the form opens it asks for: compound, dose, route, day of onset, severity, whether you discontinued, resolution, and free text. No name. No medical record. Cycle logging is here.