Does TREPROSTINIL Cause Subdural haematoma? 75 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 75 reports of Subdural haematoma have been filed in association with TREPROSTINIL (TYVASO). This represents 0.1% of all adverse event reports for TREPROSTINIL.
75
Reports of Subdural haematoma with TREPROSTINIL
0.1%
of all TREPROSTINIL reports
20
Deaths
67
Hospitalizations
How Dangerous Is Subdural haematoma From TREPROSTINIL?
Of the 75 reports, 20 (26.7%) resulted in death, 67 (89.3%) required hospitalization, and 9 (12.0%) were considered life-threatening.
Is Subdural haematoma Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 75 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 Subdural haematoma?
RIVAROXABAN (1,423)
ASPIRIN (1,181)
APIXABAN (1,025)
WARFARIN (1,012)
CLOPIDOGREL BISULFATE (809)
DABIGATRAN ETEXILATE (648)
IBRUTINIB (342)
HEPARIN (201)
ENOXAPARIN (156)
CYCLOPHOSPHAMIDE (146)
Which TREPROSTINIL Alternatives Have Lower Subdural haematoma Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE