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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 Anaemia? 991 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 991 reports of Anaemia have been filed in association with TREPROSTINIL (TYVASO). This represents 1.1% of all adverse event reports for TREPROSTINIL.

991
Reports of Anaemia with TREPROSTINIL
1.1%
of all TREPROSTINIL reports
78
Deaths
679
Hospitalizations

How Dangerous Is Anaemia From TREPROSTINIL?

Of the 991 reports, 78 (7.9%) resulted in death, 679 (68.5%) required hospitalization, and 30 (3.0%) were considered life-threatening.

Is Anaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 991 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 Anaemia?

LENALIDOMIDE (5,322) CARBOPLATIN (5,312) RIBAVIRIN (5,130) ASPIRIN (4,568) CYCLOPHOSPHAMIDE (4,486) RITUXIMAB (4,399) DEXAMETHASONE (4,352) ADALIMUMAB (3,994) PACLITAXEL (3,949) METHOTREXATE (3,913)

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