Does REPAGLINIDE Cause Wrong patient received product? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Wrong patient received product have been filed in association with REPAGLINIDE (Repaglinide). This represents 0.8% of all adverse event reports for REPAGLINIDE.
20
Reports of Wrong patient received product with REPAGLINIDE
0.8%
of all REPAGLINIDE reports
8
Deaths
9
Hospitalizations
How Dangerous Is Wrong patient received product From REPAGLINIDE?
Of the 20 reports, 8 (40.0%) resulted in death, 9 (45.0%) required hospitalization.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REPAGLINIDE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does REPAGLINIDE Cause?
Hypoglycaemia (665)
Acute kidney injury (281)
Lactic acidosis (163)
Hypoglycaemic coma (125)
Sopor (91)
Confusional state (89)
Drug interaction (89)
Blood glucose increased (88)
Diarrhoea (87)
Dyspnoea (87)
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 REPAGLINIDE Alternatives Have Lower Wrong patient received product Risk?
REPAGLINIDE vs REPOTRECTINIB
REPAGLINIDE vs REQUIP
REPAGLINIDE vs RESLIZUMAB
REPAGLINIDE vs RESMETIROM
REPAGLINIDE vs RESTASIS