Does TREPROSTINIL Cause Device use error? 563 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 563 reports of Device use error have been filed in association with TREPROSTINIL (TYVASO). This represents 0.6% of all adverse event reports for TREPROSTINIL.
563
Reports of Device use error with TREPROSTINIL
0.6%
of all TREPROSTINIL reports
18
Deaths
152
Hospitalizations
How Dangerous Is Device use error From TREPROSTINIL?
Of the 563 reports, 18 (3.2%) resulted in death, 152 (27.0%) required hospitalization, and 11 (2.0%) were considered life-threatening.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 563 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 use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which TREPROSTINIL Alternatives Have Lower Device use error Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE