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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 Condition aggravated? 157 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 157 reports of Condition aggravated have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.8% of all adverse event reports for SITAGLIPTIN.

157
Reports of Condition aggravated with SITAGLIPTIN
0.8%
of all SITAGLIPTIN reports
24
Deaths
101
Hospitalizations

How Dangerous Is Condition aggravated From SITAGLIPTIN?

Of the 157 reports, 24 (15.3%) resulted in death, 101 (64.3%) required hospitalization, and 30 (19.1%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 157 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which SITAGLIPTIN Alternatives Have Lower Condition aggravated 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 Condition aggravated Reports All Drugs Causing Condition aggravated SITAGLIPTIN Demographics