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Protein pump inhibitor. ›
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: 10
Most-reported reactions
Anaemia Of Chronic Disease — 1 report (10%) Arthropathy — 1 report (10%) Back Pain — 1 report (10%) Benign Prostatic Hyperplasia — 1 report (10%) Bk Virus Infection — 1 report (10%) Carotid Bruit — 1 report (10%) Diabetes Mellitus — 1 report (10%) Diarrhoea — 1 report (10%) Hyperlipidaemia — 1 report (10%) Hyperparathyroidism — 1 report (10%)
Source database →
Protein pump inhibitor. 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 Protein pump inhibitor. approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Protein pump inhibitor. in United States?
Odense University Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.