Does EPOPROSTENOL Cause Application site reaction? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Application site reaction have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 0.1% of all adverse event reports for EPOPROSTENOL.
13
Reports of Application site reaction with EPOPROSTENOL
0.1%
of all EPOPROSTENOL reports
2
Deaths
11
Hospitalizations
How Dangerous Is Application site reaction From EPOPROSTENOL?
Of the 13 reports, 2 (15.4%) resulted in death, 11 (84.6%) required hospitalization.
Is Application site reaction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 13 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 Application site reaction?
NICOTINE (640)
BUPRENORPHINE (503)
FENTANYL (223)
CHLORHEXIDINE\ISOPROPYL ALCOHOL (216)
MINOXIDIL (179)
INGENOL MEBUTATE (160)
ESTRADIOL (157)
ROTIGOTINE (110)
SUMATRIPTAN (86)
DICLOFENAC (72)
Which EPOPROSTENOL Alternatives Have Lower Application site reaction 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