Does EPOPROSTENOL Cause Condition aggravated? 818 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 818 reports of Condition aggravated have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 6.1% of all adverse event reports for EPOPROSTENOL.
818
Reports of Condition aggravated with EPOPROSTENOL
6.1%
of all EPOPROSTENOL reports
289
Deaths
648
Hospitalizations
How Dangerous Is Condition aggravated From EPOPROSTENOL?
Of the 818 reports, 289 (35.3%) resulted in death, 648 (79.2%) required hospitalization, and 63 (7.7%) 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 EPOPROSTENOL. However, 818 reports have been filed with the FAERS database.
What Other Side Effects Does EPOPROSTENOL Cause?
Dyspnoea (2,744)
Headache (2,425)
Diarrhoea (2,310)
Nausea (2,016)
Pain in jaw (1,928)
Death (1,362)
Flushing (1,256)
Fatigue (1,133)
Hospitalisation (1,078)
Vomiting (1,068)
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 EPOPROSTENOL Alternatives Have Lower Condition aggravated Risk?
EPOPROSTENOL vs EPTIFIBATIDE
EPOPROSTENOL vs EPTINEZUMAB-JJMR
EPOPROSTENOL vs EPTINEZUMAB\EPTINEZUMAB-JJMR
EPOPROSTENOL vs EQUINE BOTULINUM NEUROTOXIN A/B/C/D/E/F/G IMMUNE FAB2
EPOPROSTENOL vs EQUINE THYMOCYTE IMMUNE GLOBULIN