🇺🇸 NPH human insulin in United States
40 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: 40
Most-reported reactions
- Hypoglycaemia — 7 reports (17.5%)
- Blood Glucose Decreased — 5 reports (12.5%)
- Blood Glucose Increased — 5 reports (12.5%)
- Cerebrovascular Accident — 4 reports (10%)
- Diabetes Mellitus Inadequate Control — 4 reports (10%)
- Pharmaceutical Product Complaint — 4 reports (10%)
- Arteriosclerosis — 3 reports (7.5%)
- Hyperglycaemia — 3 reports (7.5%)
- Pleural Effusion — 3 reports (7.5%)
- Alanine Aminotransferase Increased — 2 reports (5%)
Other Diabetes approved in United States
Frequently asked questions
Is NPH human insulin approved in United States?
NPH human insulin does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for NPH human insulin in United States?
Sanofi is the originator. The local marketing authorisation holder may differ — check the official source linked above.