Drug Landscape ›
glargine insulin ›
Regulatory · United States
Marketing authorisation
FDA
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: 20 April 2025 – 20 April 2026
Total reports: 233
Most-reported reactions
Nausea — 29 reports (12.45%) Blood Glucose Increased — 27 reports (11.59%) Renal Failure Acute — 25 reports (10.73%) Diarrhoea — 24 reports (10.3%) Vomiting — 24 reports (10.3%) Drug Interaction — 22 reports (9.44%) Fall — 22 reports (9.44%) Hypoglycaemia — 22 reports (9.44%) Anaemia — 19 reports (8.15%) Dehydration — 19 reports (8.15%)
Source database →
glargine insulin in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Frequently asked questions
Is glargine insulin approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for glargine insulin in United States?
Baylor College of Medicine is the originator. The local marketing authorisation holder may differ — check the official source linked above.