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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 Dermatitis contact? 1,834 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,834 reports of Dermatitis contact have been filed in association with TREPROSTINIL (TYVASO). This represents 2.0% of all adverse event reports for TREPROSTINIL.

1,834
Reports of Dermatitis contact with TREPROSTINIL
2.0%
of all TREPROSTINIL reports
17
Deaths
376
Hospitalizations

How Dangerous Is Dermatitis contact From TREPROSTINIL?

Of the 1,834 reports, 17 (0.9%) resulted in death, 376 (20.5%) required hospitalization, and 5 (0.3%) were considered life-threatening.

Is Dermatitis contact Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 1,834 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 Dermatitis contact?

DUPILUMAB (358) HUMAN IMMUNOGLOBULIN G (345) ADALIMUMAB (321) EPOPROSTENOL (190) ETANERCEPT (170) NICOTINE (163) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (160) AMBRISENTAN (147) CHLORHEXIDINE\ISOPROPYL ALCOHOL (146) ESTRADIOL (146)

Which TREPROSTINIL Alternatives Have Lower Dermatitis contact 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 Dermatitis contact Reports All Drugs Causing Dermatitis contact TREPROSTINIL Demographics