Does GLIMEPIRIDE Cause Wrong patient received product? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong patient received product have been filed in association with GLIMEPIRIDE (Glimepiride). This represents 0.1% of all adverse event reports for GLIMEPIRIDE.
5
Reports of Wrong patient received product with GLIMEPIRIDE
0.1%
of all GLIMEPIRIDE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Wrong patient received product From GLIMEPIRIDE?
Of the 5 reports, 5 (100.0%) required hospitalization, and 2 (40.0%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLIMEPIRIDE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does GLIMEPIRIDE Cause?
Hypoglycaemia (1,403)
Blood glucose increased (446)
Acute kidney injury (339)
Drug ineffective (339)
Diarrhoea (257)
Blood glucose decreased (232)
Lactic acidosis (219)
Glycosylated haemoglobin increased (214)
Diabetes mellitus inadequate control (213)
Hypoglycaemic coma (187)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which GLIMEPIRIDE Alternatives Have Lower Wrong patient received product Risk?
GLIMEPIRIDE vs GLIMEPIRIDE\ROSIGLITAZONE
GLIMEPIRIDE vs GLIPIZIDE
GLIMEPIRIDE vs GLIVEC
GLIMEPIRIDE vs GLOFITAMAB
GLIMEPIRIDE vs GLOFITAMAB-GXBM