Does TREPROSTINIL Cause Full blood count decreased? 86 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 86 reports of Full blood count decreased have been filed in association with TREPROSTINIL (TYVASO). This represents 0.1% of all adverse event reports for TREPROSTINIL.
86
Reports of Full blood count decreased with TREPROSTINIL
0.1%
of all TREPROSTINIL reports
6
Deaths
66
Hospitalizations
How Dangerous Is Full blood count decreased From TREPROSTINIL?
Of the 86 reports, 6 (7.0%) resulted in death, 66 (76.7%) required hospitalization, and 3 (3.5%) were considered life-threatening.
Is Full blood count decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 86 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 Full blood count decreased?
LENALIDOMIDE (6,059)
PALBOCICLIB (1,964)
POMALIDOMIDE (1,599)
RUXOLITINIB (469)
VENETOCLAX (424)
NIRAPARIB (356)
REVLIMID (352)
ADALIMUMAB (212)
IXAZOMIB (196)
DEXAMETHASONE (184)
Which TREPROSTINIL Alternatives Have Lower Full blood count decreased Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE