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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 Sepsis? 878 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 878 reports of Sepsis have been filed in association with TREPROSTINIL (TYVASO). This represents 1.0% of all adverse event reports for TREPROSTINIL.

878
Reports of Sepsis with TREPROSTINIL
1.0%
of all TREPROSTINIL reports
220
Deaths
808
Hospitalizations

How Dangerous Is Sepsis From TREPROSTINIL?

Of the 878 reports, 220 (25.1%) resulted in death, 808 (92.0%) required hospitalization, and 67 (7.6%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 878 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 Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

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