Does SITAGLIPTIN Cause Adverse event? 381 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 381 reports of Adverse event have been filed in association with SITAGLIPTIN (JANUVIA). This represents 1.9% of all adverse event reports for SITAGLIPTIN.
381
Reports of Adverse event with SITAGLIPTIN
1.9%
of all SITAGLIPTIN reports
59
Deaths
176
Hospitalizations
How Dangerous Is Adverse event From SITAGLIPTIN?
Of the 381 reports, 59 (15.5%) resulted in death, 176 (46.2%) required hospitalization, and 6 (1.6%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 381 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which SITAGLIPTIN Alternatives Have Lower Adverse event Risk?
SITAGLIPTIN vs SOAP
SITAGLIPTIN vs SODIUM
SITAGLIPTIN vs SODIUM BICARBONATE
SITAGLIPTIN vs SODIUM BICARBONATE\SODIUM
SITAGLIPTIN vs SODIUM BORATE