🇺🇸 Insulin lispro (Humalog) in United States
49 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: 22 April 2025 – 22 April 2026
- Total reports: 49
Most-reported reactions
- Blood Glucose Increased — 7 reports (14.29%)
- Asthenia — 6 reports (12.24%)
- Dyspnoea — 6 reports (12.24%)
- Fall — 6 reports (12.24%)
- Hypoglycaemia — 6 reports (12.24%)
- Cerebrovascular Accident — 4 reports (8.16%)
- Diarrhoea — 4 reports (8.16%)
- Fatigue — 4 reports (8.16%)
- Hyperglycaemia — 3 reports (6.12%)
- Hypotension — 3 reports (6.12%)
Other Diabetes approved in United States
Frequently asked questions
Is Insulin lispro (Humalog) approved in United States?
Insulin lispro (Humalog) does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Insulin lispro (Humalog) in United States?
Eli Lilly and Company is the originator. The local marketing authorisation holder may differ — check the official source linked above.