Does TREPROSTINIL Cause Condition aggravated? 1,741 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,741 reports of Condition aggravated have been filed in association with TREPROSTINIL (TYVASO). This represents 1.9% of all adverse event reports for TREPROSTINIL.
1,741
Reports of Condition aggravated with TREPROSTINIL
1.9%
of all TREPROSTINIL reports
259
Deaths
782
Hospitalizations
How Dangerous Is Condition aggravated From TREPROSTINIL?
Of the 1,741 reports, 259 (14.9%) resulted in death, 782 (44.9%) required hospitalization, and 62 (3.6%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 1,741 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which TREPROSTINIL Alternatives Have Lower Condition aggravated Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE