🇺🇸 Januvia (sitagliptin) in United States
266 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: 266
Most-reported reactions
- Pancreatitis — 78 reports (29.32%)
- Bladder Cancer — 33 reports (12.41%)
- Nausea — 25 reports (9.4%)
- Diarrhoea — 24 reports (9.02%)
- Renal Failure — 22 reports (8.27%)
- Blood Glucose Increased — 21 reports (7.89%)
- Fatigue — 17 reports (6.39%)
- Dyspnoea — 16 reports (6.02%)
- Constipation — 15 reports (5.64%)
- Renal Failure Acute — 15 reports (5.64%)
Other Diabetes approved in United States
Frequently asked questions
Is Januvia (sitagliptin) approved in United States?
Januvia (sitagliptin) does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Januvia (sitagliptin) in United States?
Zealand University Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.