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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 Product quality issue? 91 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Product quality issue have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.5% of all adverse event reports for SITAGLIPTIN.

91
Reports of Product quality issue with SITAGLIPTIN
0.5%
of all SITAGLIPTIN reports
1
Deaths
9
Hospitalizations

How Dangerous Is Product quality issue From SITAGLIPTIN?

Of the 91 reports, 1 (1.1%) resulted in death, 9 (9.9%) required hospitalization, and 2 (2.2%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 91 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) 503 Service Unavailable

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