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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 Full blood count abnormal? 104 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 104 reports of Full blood count abnormal have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.5% of all adverse event reports for SITAGLIPTIN.

104
Reports of Full blood count abnormal with SITAGLIPTIN
0.5%
of all SITAGLIPTIN reports
1
Deaths
12
Hospitalizations

How Dangerous Is Full blood count abnormal From SITAGLIPTIN?

Of the 104 reports, 1 (1.0%) resulted in death, 12 (11.5%) required hospitalization, and 1 (1.0%) were considered life-threatening.

Is Full blood count abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 104 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 Full blood count abnormal?

ALBUTEROL (3,060) PREDNISONE (2,230) BUDESONIDE\FORMOTEROL (1,786) TIOTROPIUM (1,754) MONTELUKAST (1,529) MEPOLIZUMAB (1,440) BUDESONIDE (1,339) PALBOCICLIB (1,146) CICLESONIDE (916) PANTOPRAZOLE (776)

Which SITAGLIPTIN Alternatives Have Lower Full blood count 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 Full blood count abnormal Reports All Drugs Causing Full blood count abnormal SITAGLIPTIN Demographics