Does TREPROSTINIL Cause Unevaluable event? 326 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 326 reports of Unevaluable event have been filed in association with TREPROSTINIL (TYVASO). This represents 0.4% of all adverse event reports for TREPROSTINIL.
326
Reports of Unevaluable event with TREPROSTINIL
0.4%
of all TREPROSTINIL reports
25
Deaths
206
Hospitalizations
How Dangerous Is Unevaluable event From TREPROSTINIL?
Of the 326 reports, 25 (7.7%) resulted in death, 206 (63.2%) required hospitalization, and 3 (0.9%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 326 reports have been filed with the FAERS database.
What Other Side Effects Does TREPROSTINIL Cause?
Dyspnoea (16,348)
Headache (14,051)
Diarrhoea (11,335)
Nausea (10,320)
Cough (8,945)
Fatigue (7,440)
Dizziness (7,405)
Infusion site pain (5,169)
Vomiting (5,097)
Death (4,764)
What Other Drugs Cause Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which TREPROSTINIL Alternatives Have Lower Unevaluable event Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE