Does METFORMIN\SITAGLIPTIN Cause Product dose omission? 185 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 185 reports of Product dose omission have been filed in association with METFORMIN\SITAGLIPTIN. This represents 2.1% of all adverse event reports for METFORMIN\SITAGLIPTIN.
185
Reports of Product dose omission with METFORMIN\SITAGLIPTIN
2.1%
of all METFORMIN\SITAGLIPTIN reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product dose omission From METFORMIN\SITAGLIPTIN?
Of the 185 reports, 7 (3.8%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METFORMIN\SITAGLIPTIN. However, 185 reports have been filed with the FAERS database.
What Other Side Effects Does METFORMIN\SITAGLIPTIN Cause?
Blood glucose increased (709)
Acute kidney injury (616)
Lactic acidosis (557)
No adverse event (539)
Diarrhoea (513)
Inappropriate schedule of drug administration (469)
Product dose omission issue (452)
Pancreatic carcinoma (431)
Drug ineffective (384)
Nausea (378)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which METFORMIN\SITAGLIPTIN Alternatives Have Lower Product dose omission Risk?
METFORMIN\SITAGLIPTIN vs METFORMIN\VILDAGLIPTIN
METFORMIN\SITAGLIPTIN vs METHADONE
METFORMIN\SITAGLIPTIN vs METHAMPHETAMINE
METFORMIN\SITAGLIPTIN vs METHENAMINE HIPPURATE
METFORMIN\SITAGLIPTIN vs METHIMAZOLE