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POTASSIUM BICARBONATE ›
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: 1,332
Most-reported reactions
Off Label Use — 181 reports (13.59%) Diarrhoea — 178 reports (13.36%) Nausea — 159 reports (11.94%) Dyspnoea — 140 reports (10.51%) Vomiting — 138 reports (10.36%) Fatigue — 135 reports (10.14%) Acute Kidney Injury — 124 reports (9.31%) Asthenia — 98 reports (7.36%) Headache — 92 reports (6.91%) Hypokalaemia — 87 reports (6.53%)
Source database →
POTASSIUM BICARBONATE 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 POTASSIUM BICARBONATE approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for POTASSIUM BICARBONATE in United States?
Marketing authorisation holder not available in our data.