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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 Acute hepatic failure? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Acute hepatic failure have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.1% of all adverse event reports for SITAGLIPTIN.

21
Reports of Acute hepatic failure with SITAGLIPTIN
0.1%
of all SITAGLIPTIN reports
19
Deaths
8
Hospitalizations

How Dangerous Is Acute hepatic failure From SITAGLIPTIN?

Of the 21 reports, 19 (90.5%) resulted in death, 8 (38.1%) required hospitalization, and 4 (19.0%) were considered life-threatening.

Is Acute hepatic failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 21 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 Acute hepatic failure?

ACETAMINOPHEN (3,141) PREDNISONE (439) IBUPROFEN (412) RITUXIMAB (412) CYCLOPHOSPHAMIDE (411) DOXORUBICIN (385) VINCRISTINE (346) PREDNISOLONE (301) METHOTREXATE (285) DEXAMETHASONE (249)

Which SITAGLIPTIN Alternatives Have Lower Acute hepatic failure 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 Acute hepatic failure Reports All Drugs Causing Acute hepatic failure SITAGLIPTIN Demographics