Does SITAGLIPTIN Cause International normalised ratio increased? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of International normalised ratio increased have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.2% of all adverse event reports for SITAGLIPTIN.
33
Reports of International normalised ratio increased with SITAGLIPTIN
0.2%
of all SITAGLIPTIN reports
12
Deaths
18
Hospitalizations
How Dangerous Is International normalised ratio increased From SITAGLIPTIN?
Of the 33 reports, 12 (36.4%) resulted in death, 18 (54.5%) required hospitalization, and 19 (57.6%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 33 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 International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which SITAGLIPTIN Alternatives Have Lower International normalised ratio increased Risk?
SITAGLIPTIN vs SOAP
SITAGLIPTIN vs SODIUM
SITAGLIPTIN vs SODIUM BICARBONATE
SITAGLIPTIN vs SODIUM BICARBONATE\SODIUM
SITAGLIPTIN vs SODIUM BORATE