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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SITAGLIPTIN Cause Hypokalaemia? 94 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of Hypokalaemia have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.5% of all adverse event reports for SITAGLIPTIN.

94
Reports of Hypokalaemia with SITAGLIPTIN
0.5%
of all SITAGLIPTIN reports
64
Deaths
88
Hospitalizations

How Dangerous Is Hypokalaemia From SITAGLIPTIN?

Of the 94 reports, 64 (68.1%) resulted in death, 88 (93.6%) required hospitalization, and 23 (24.5%) were considered life-threatening.

Is Hypokalaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 94 reports have been filed with the FAERS database.

What Other Side Effects Does SITAGLIPTIN Cause?

Blood glucose increased (1,427) Pancreatic carcinoma (1,142) Product dose omission issue (1,125) Drug ineffective (1,057) No adverse event (994) Nausea (936) Pancreatitis (922) Diabetes mellitus inadequate control (744) Diarrhoea (712) Hypoglycaemia (674)

What Other Drugs Cause Hypokalaemia?

FUROSEMIDE (2,503) HYDROCHLOROTHIAZIDE (1,152) CARBOPLATIN (1,118) PREDNISONE (967) DEXAMETHASONE (876) CYCLOPHOSPHAMIDE (864) OMEPRAZOLE (851) RITUXIMAB (822) AMLODIPINE (815) PANTOPRAZOLE (811)

Which SITAGLIPTIN Alternatives Have Lower Hypokalaemia Risk?

SITAGLIPTIN vs SOAP SITAGLIPTIN vs SODIUM SITAGLIPTIN vs SODIUM BICARBONATE SITAGLIPTIN vs SODIUM BICARBONATE\SODIUM SITAGLIPTIN vs SODIUM BORATE

Related Pages

SITAGLIPTIN Full Profile All Hypokalaemia Reports All Drugs Causing Hypokalaemia SITAGLIPTIN Demographics