Does TREPROSTINIL Cause Device dislocation? 1,626 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,626 reports of Device dislocation have been filed in association with TREPROSTINIL (TYVASO). This represents 1.8% of all adverse event reports for TREPROSTINIL.
1,626
Reports of Device dislocation with TREPROSTINIL
1.8%
of all TREPROSTINIL reports
52
Deaths
705
Hospitalizations
How Dangerous Is Device dislocation From TREPROSTINIL?
Of the 1,626 reports, 52 (3.2%) resulted in death, 705 (43.4%) required hospitalization, and 18 (1.1%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 1,626 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 Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
DEXAMETHASONE (290)
Which TREPROSTINIL Alternatives Have Lower Device dislocation Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE