Does EPOPROSTENOL Cause International normalised ratio increased? 54 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 54 reports of International normalised ratio increased have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 0.4% of all adverse event reports for EPOPROSTENOL.
54
Reports of International normalised ratio increased with EPOPROSTENOL
0.4%
of all EPOPROSTENOL reports
7
Deaths
40
Hospitalizations
How Dangerous Is International normalised ratio increased From EPOPROSTENOL?
Of the 54 reports, 7 (13.0%) resulted in death, 40 (74.1%) required hospitalization.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 54 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 International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which EPOPROSTENOL Alternatives Have Lower International normalised ratio increased 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