Drug Landscape ›
Basal bolus 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: 16
Most-reported reactions
Diabetic Ketoacidosis — 3 reports (18.75%) Blood Triglycerides Increased — 2 reports (12.5%) Caesarean Section — 2 reports (12.5%) Hyperglycaemia — 2 reports (12.5%) Off Label Use — 2 reports (12.5%) Blood Creatinine Increased — 1 report (6.25%) Drug Ineffective — 1 report (6.25%) Drug Interaction — 1 report (6.25%) Drug Level Increased — 1 report (6.25%) Exposure During Pregnancy — 1 report (6.25%)
Source database →
Basal bolus 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 Basal bolus insulin approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Basal bolus insulin in United States?
Emory University is the originator. The local marketing authorisation holder may differ — check the official source linked above.