🇺🇸 LOXO-305 in United States
7 US adverse-event reports
Safety signals — FAERS
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
- Window: 23 April 2025 – 23 April 2026
- Total reports: 7
Most-reported reactions
- Fall — 1 report (14.29%)
- Haematochezia — 1 report (14.29%)
- Hypertension — 1 report (14.29%)
- Hypertensive Urgency — 1 report (14.29%)
- Infusion Related Reaction — 1 report (14.29%)
- Small Intestinal Obstruction — 1 report (14.29%)
- Subdural Haematoma — 1 report (14.29%)
Other Oncology approved in United States
Frequently asked questions
Is LOXO-305 approved in United States?
LOXO-305 does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for LOXO-305 in United States?
Eli Lilly and Company is the originator. The local marketing authorisation holder may differ — check the official source linked above.