Does REPAGLINIDE Cause Condition aggravated? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Condition aggravated have been filed in association with REPAGLINIDE (Repaglinide). This represents 1.9% of all adverse event reports for REPAGLINIDE.
47
Reports of Condition aggravated with REPAGLINIDE
1.9%
of all REPAGLINIDE reports
21
Deaths
8
Hospitalizations
How Dangerous Is Condition aggravated From REPAGLINIDE?
Of the 47 reports, 21 (44.7%) resulted in death, 8 (17.0%) required hospitalization, and 19 (40.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REPAGLINIDE. However, 47 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which REPAGLINIDE Alternatives Have Lower Condition aggravated Risk?
REPAGLINIDE vs REPOTRECTINIB
REPAGLINIDE vs REQUIP
REPAGLINIDE vs RESLIZUMAB
REPAGLINIDE vs RESMETIROM
REPAGLINIDE vs RESTASIS