Does SITAGLIPTIN Cause Drug dose omission? 294 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 294 reports of Drug dose omission have been filed in association with SITAGLIPTIN (JANUVIA). This represents 1.5% of all adverse event reports for SITAGLIPTIN.
294
Reports of Drug dose omission with SITAGLIPTIN
1.5%
of all SITAGLIPTIN reports
0
Deaths
28
Hospitalizations
How Dangerous Is Drug dose omission From SITAGLIPTIN?
Of the 294 reports, 28 (9.5%) required hospitalization, and 4 (1.4%) were considered life-threatening.
Is Drug dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 294 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 Drug dose omission?
ETANERCEPT (10,871)
CINACALCET (8,683)
EVOLOCUMAB (4,914)
ADALIMUMAB (3,993)
INSULIN LISPRO (3,063)
GOLIMUMAB (2,652)
TERIPARATIDE (2,616)
APREMILAST (2,466)
ALBUTEROL (2,309)
FLUTICASONE\SALMETEROL (2,153)
Which SITAGLIPTIN Alternatives Have Lower Drug dose omission Risk?
SITAGLIPTIN vs SOAP
SITAGLIPTIN vs SODIUM
SITAGLIPTIN vs SODIUM BICARBONATE
SITAGLIPTIN vs SODIUM BICARBONATE\SODIUM
SITAGLIPTIN vs SODIUM BORATE