Does EPTIFIBATIDE Cause Condition aggravated? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Condition aggravated have been filed in association with EPTIFIBATIDE (Eptifibatide). This represents 3.0% of all adverse event reports for EPTIFIBATIDE.
14
Reports of Condition aggravated with EPTIFIBATIDE
3.0%
of all EPTIFIBATIDE reports
7
Deaths
10
Hospitalizations
How Dangerous Is Condition aggravated From EPTIFIBATIDE?
Of the 14 reports, 7 (50.0%) resulted in death, 10 (71.4%) required hospitalization, and 5 (35.7%) 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 EPTIFIBATIDE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does EPTIFIBATIDE Cause?
Product use in unapproved indication (61)
Thrombocytopenia (58)
Drug ineffective (39)
Off label use (31)
Haemoglobin decreased (30)
Haemorrhage (28)
Vascular stent thrombosis (19)
Gastrointestinal haemorrhage (14)
Haematoma (14)
Product use issue (14)
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 EPTIFIBATIDE Alternatives Have Lower Condition aggravated Risk?
EPTIFIBATIDE vs EPTINEZUMAB-JJMR
EPTIFIBATIDE vs EPTINEZUMAB\EPTINEZUMAB-JJMR
EPTIFIBATIDE vs EQUINE THYMOCYTE IMMUNE GLOBULIN
EPTIFIBATIDE vs ERAVACYCLINE
EPTIFIBATIDE vs ERBITUX