Does SITAGLIPTIN Cause Poor quality product administered? 44 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Poor quality product administered have been filed in association with SITAGLIPTIN (JANUVIA). This represents 0.2% of all adverse event reports for SITAGLIPTIN.
44
Reports of Poor quality product administered with SITAGLIPTIN
0.2%
of all SITAGLIPTIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Poor quality product administered From SITAGLIPTIN?
Of the 44 reports, 2 (4.5%) required hospitalization, and 1 (2.3%) were considered life-threatening.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SITAGLIPTIN. However, 44 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which SITAGLIPTIN Alternatives Have Lower Poor quality product administered Risk?
SITAGLIPTIN vs SOAP
SITAGLIPTIN vs SODIUM
SITAGLIPTIN vs SODIUM BICARBONATE
SITAGLIPTIN vs SODIUM BICARBONATE\SODIUM
SITAGLIPTIN vs SODIUM BORATE