Does TREPROSTINIL Cause Complication associated with device? 422 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 422 reports of Complication associated with device have been filed in association with TREPROSTINIL (TYVASO). This represents 0.5% of all adverse event reports for TREPROSTINIL.
422
Reports of Complication associated with device with TREPROSTINIL
0.5%
of all TREPROSTINIL reports
29
Deaths
317
Hospitalizations
How Dangerous Is Complication associated with device From TREPROSTINIL?
Of the 422 reports, 29 (6.9%) resulted in death, 317 (75.1%) required hospitalization, and 13 (3.1%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 422 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
AMBRISENTAN (125)
Which TREPROSTINIL Alternatives Have Lower Complication associated with device Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE