Does TREPROSTINIL Cause Haematemesis? 202 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 202 reports of Haematemesis have been filed in association with TREPROSTINIL (TYVASO). This represents 0.2% of all adverse event reports for TREPROSTINIL.
202
Reports of Haematemesis with TREPROSTINIL
0.2%
of all TREPROSTINIL reports
25
Deaths
162
Hospitalizations
How Dangerous Is Haematemesis From TREPROSTINIL?
Of the 202 reports, 25 (12.4%) resulted in death, 162 (80.2%) required hospitalization, and 11 (5.4%) were considered life-threatening.
Is Haematemesis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 202 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 Haematemesis?
ASPIRIN (1,538)
RIVAROXABAN (1,085)
CLOPIDOGREL BISULFATE (954)
IBUPROFEN (836)
APIXABAN (650)
ADALIMUMAB (563)
ACETAMINOPHEN (454)
WARFARIN (426)
SERTRALINE (412)
ENOXAPARIN (404)
Which TREPROSTINIL Alternatives Have Lower Haematemesis Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE