Does EPOPROSTENOL Cause Application site irritation? 48 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Application site irritation have been filed in association with EPOPROSTENOL (EPOPROSTENOL). This represents 0.4% of all adverse event reports for EPOPROSTENOL.
48
Reports of Application site irritation with EPOPROSTENOL
0.4%
of all EPOPROSTENOL reports
7
Deaths
40
Hospitalizations
How Dangerous Is Application site irritation From EPOPROSTENOL?
Of the 48 reports, 7 (14.6%) resulted in death, 40 (83.3%) required hospitalization.
Is Application site irritation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPOPROSTENOL. However, 48 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 irritation?
MINOXIDIL (1,826)
BUPRENORPHINE (921)
ESTRADIOL (624)
NICOTINE (539)
SUMATRIPTAN (392)
TESTOSTERONE (390)
ESTRADIOL\NORETHINDRONE (341)
FENTANYL (271)
METHYLPHENIDATE (235)
ETHINYL ESTRADIOL\NORELGESTROMIN (139)
Which EPOPROSTENOL Alternatives Have Lower Application site irritation 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