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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 Hepatic function abnormal? 61 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Hepatic function abnormal have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.3% of all adverse event reports for SITAGLIPTIN.

61
Reports of Hepatic function abnormal with SITAGLIPTIN
0.3%
of all SITAGLIPTIN reports
7
Deaths
38
Hospitalizations

How Dangerous Is Hepatic function abnormal From SITAGLIPTIN?

Of the 61 reports, 7 (11.5%) resulted in death, 38 (62.3%) required hospitalization, and 2 (3.3%) were considered life-threatening.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 61 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 Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which SITAGLIPTIN Alternatives Have Lower Hepatic function abnormal 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 Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal SITAGLIPTIN Demographics