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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 Respiratory distress? 345 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 345 reports of Respiratory distress have been filed in association with TREPROSTINIL (TYVASO). This represents 0.4% of all adverse event reports for TREPROSTINIL.

345
Reports of Respiratory distress with TREPROSTINIL
0.4%
of all TREPROSTINIL reports
85
Deaths
324
Hospitalizations

How Dangerous Is Respiratory distress From TREPROSTINIL?

Of the 345 reports, 85 (24.6%) resulted in death, 324 (93.9%) required hospitalization, and 43 (12.5%) were considered life-threatening.

Is Respiratory distress Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 345 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 Respiratory distress?

PREDNISONE (519) CYCLOPHOSPHAMIDE (496) METHOTREXATE (445) DEXAMETHASONE (431) RITUXIMAB (420) TACROLIMUS (376) ALBUTEROL (355) VINCRISTINE (342) PREDNISOLONE (298) METHYLPREDNISOLONE (290)

Which TREPROSTINIL Alternatives Have Lower Respiratory distress 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 Respiratory distress Reports All Drugs Causing Respiratory distress TREPROSTINIL Demographics