Does TREPROSTINIL Cause Product administration interrupted? 295 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 295 reports of Product administration interrupted have been filed in association with TREPROSTINIL (TYVASO). This represents 0.3% of all adverse event reports for TREPROSTINIL.
295
Reports of Product administration interrupted with TREPROSTINIL
0.3%
of all TREPROSTINIL reports
14
Deaths
108
Hospitalizations
How Dangerous Is Product administration interrupted From TREPROSTINIL?
Of the 295 reports, 14 (4.7%) resulted in death, 108 (36.6%) required hospitalization, and 10 (3.4%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 295 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 Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
ADALIMUMAB (86)
Which TREPROSTINIL Alternatives Have Lower Product administration interrupted Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE