Does GLIMEPIRIDE Cause Intentional product misuse? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Intentional product misuse have been filed in association with GLIMEPIRIDE (Glimepiride). This represents 0.7% of all adverse event reports for GLIMEPIRIDE.
40
Reports of Intentional product misuse with GLIMEPIRIDE
0.7%
of all GLIMEPIRIDE reports
1
Deaths
28
Hospitalizations
How Dangerous Is Intentional product misuse From GLIMEPIRIDE?
Of the 40 reports, 1 (2.5%) resulted in death, 28 (70.0%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLIMEPIRIDE. However, 40 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which GLIMEPIRIDE Alternatives Have Lower Intentional product misuse Risk?
GLIMEPIRIDE vs GLIMEPIRIDE\ROSIGLITAZONE
GLIMEPIRIDE vs GLIPIZIDE
GLIMEPIRIDE vs GLIVEC
GLIMEPIRIDE vs GLOFITAMAB
GLIMEPIRIDE vs GLOFITAMAB-GXBM