Does EPOPROSTENOL Cause Product administration interrupted? 205 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 205 reports of Product administration interrupted have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 1.5% of all adverse event reports for EPOPROSTENOL.
205
Reports of Product administration interrupted with EPOPROSTENOL
1.5%
of all EPOPROSTENOL reports
5
Deaths
171
Hospitalizations
How Dangerous Is Product administration interrupted From EPOPROSTENOL?
Of the 205 reports, 5 (2.4%) resulted in death, 171 (83.4%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 205 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 Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
ADALIMUMAB (86)
Which EPOPROSTENOL Alternatives Have Lower Product administration interrupted 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