Does TREPROSTINIL Cause Device issue? 1,636 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,636 reports of Device issue have been filed in association with TREPROSTINIL (TYVASO). This represents 1.8% of all adverse event reports for TREPROSTINIL.
1,636
Reports of Device issue with TREPROSTINIL
1.8%
of all TREPROSTINIL reports
42
Deaths
460
Hospitalizations
How Dangerous Is Device issue From TREPROSTINIL?
Of the 1,636 reports, 42 (2.6%) resulted in death, 460 (28.1%) required hospitalization, and 16 (1.0%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 1,636 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which TREPROSTINIL Alternatives Have Lower Device issue Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE