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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TREPROSTINIL Cause Device maintenance issue? 402 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 402 reports of Device maintenance issue have been filed in association with TREPROSTINIL (TYVASO). This represents 0.4% of all adverse event reports for TREPROSTINIL.

402
Reports of Device maintenance issue with TREPROSTINIL
0.4%
of all TREPROSTINIL reports
4
Deaths
62
Hospitalizations

How Dangerous Is Device maintenance issue From TREPROSTINIL?

Of the 402 reports, 4 (1.0%) resulted in death, 62 (15.4%) required hospitalization, and 4 (1.0%) were considered life-threatening.

Is Device maintenance issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 402 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 maintenance issue?

AMIKACIN (28) ALBUTEROL (22) LECITHIN\POLOXAMER 407 (18) SOTATERCEPT (12) ACETAMINOPHEN (11) SELEXIPAG (11) MACITENTAN (10) RIOCIGUAT (10) GABAPENTIN (8) SOMATROPIN (6)

Which TREPROSTINIL Alternatives Have Lower Device maintenance issue Risk?

TREPROSTINIL vs TREPROSTINIL DIOLAMINE TREPROSTINIL vs TRETINOIN TREPROSTINIL vs TRIAMCINOLONE TREPROSTINIL vs TRIAMCINOLONE ACETONIDE TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE

Related Pages

TREPROSTINIL Full Profile All Device maintenance issue Reports All Drugs Causing Device maintenance issue TREPROSTINIL Demographics