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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 Hospitalisation? 496 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 496 reports of Hospitalisation have been filed in association with TREPROSTINIL (TYVASO). This represents 0.5% of all adverse event reports for TREPROSTINIL.

496
Reports of Hospitalisation with TREPROSTINIL
0.5%
of all TREPROSTINIL reports
59
Deaths
493
Hospitalizations

How Dangerous Is Hospitalisation From TREPROSTINIL?

Of the 496 reports, 59 (11.9%) resulted in death, 493 (99.4%) required hospitalization, and 9 (1.8%) were considered life-threatening.

Is Hospitalisation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 496 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 Hospitalisation?

CLOZAPINE (12,144) CINACALCET (6,997) DARBEPOETIN ALFA (5,682) MACITENTAN (3,414) APIXABAN (3,315) ADALIMUMAB (3,033) DUPILUMAB (2,529) LENALIDOMIDE (2,241) DENOSUMAB (2,076) PALIPERIDONE (2,066)

Which TREPROSTINIL Alternatives Have Lower Hospitalisation 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 Hospitalisation Reports All Drugs Causing Hospitalisation TREPROSTINIL Demographics