Does METFORMIN Cause Product dose omission issue? 440 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 440 reports of Product dose omission issue have been filed in association with METFORMIN (Metformin Hydrochloride). This represents 0.5% of all adverse event reports for METFORMIN.
440
Reports of Product dose omission issue with METFORMIN
0.5%
of all METFORMIN reports
1
Deaths
175
Hospitalizations
How Dangerous Is Product dose omission issue From METFORMIN?
Of the 440 reports, 1 (0.2%) resulted in death, 175 (39.8%) required hospitalization, and 20 (4.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METFORMIN. However, 440 reports have been filed with the FAERS database.
What Other Side Effects Does METFORMIN Cause?
Lactic acidosis (16,316)
Acute kidney injury (11,361)
Diarrhoea (7,679)
Toxicity to various agents (5,669)
Metabolic acidosis (5,236)
Hypoglycaemia (5,047)
Drug ineffective (4,991)
Nausea (4,915)
Vomiting (4,624)
Blood glucose increased (4,038)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which METFORMIN Alternatives Have Lower Product dose omission issue Risk?
METFORMIN vs METFORMIN\PIOGLITAZONE
METFORMIN vs METFORMIN\ROSIGLITAZONE
METFORMIN vs METFORMIN\SAXAGLIPTIN
METFORMIN vs METFORMIN\SITAGLIPTIN
METFORMIN vs METFORMIN\VILDAGLIPTIN