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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 Adverse event? 237 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 237 reports of Adverse event have been filed in association with TREPROSTINIL (TYVASO). This represents 0.3% of all adverse event reports for TREPROSTINIL.

237
Reports of Adverse event with TREPROSTINIL
0.3%
of all TREPROSTINIL reports
14
Deaths
101
Hospitalizations

How Dangerous Is Adverse event From TREPROSTINIL?

Of the 237 reports, 14 (5.9%) resulted in death, 101 (42.6%) required hospitalization, and 3 (1.3%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for TREPROSTINIL.

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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which TREPROSTINIL Alternatives Have Lower Adverse event 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 Adverse event Reports All Drugs Causing Adverse event TREPROSTINIL Demographics