Does EPOPROSTENOL Cause Device occlusion? 580 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 580 reports of Device occlusion have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 4.4% of all adverse event reports for EPOPROSTENOL.
580
Reports of Device occlusion with EPOPROSTENOL
4.4%
of all EPOPROSTENOL reports
48
Deaths
507
Hospitalizations
How Dangerous Is Device occlusion From EPOPROSTENOL?
Of the 580 reports, 48 (8.3%) resulted in death, 507 (87.4%) required hospitalization, and 24 (4.1%) were considered life-threatening.
Is Device occlusion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 580 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 Device occlusion?
PEGFILGRASTIM (3,239)
CARBIDOPA\LEVODOPA (1,464)
SOMATROPIN (823)
LEUPROLIDE (786)
TREPROSTINIL (458)
ALBUTEROL (431)
MEDROXYPROGESTERONE (284)
BACLOFEN (254)
LEVODOPA (224)
RISPERIDONE (182)
Which EPOPROSTENOL Alternatives Have Lower Device occlusion 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