Does TREPROSTINIL Cause Decreased activity? 195 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 195 reports of Decreased activity have been filed in association with TREPROSTINIL (TYVASO). This represents 0.2% of all adverse event reports for TREPROSTINIL.
195
Reports of Decreased activity with TREPROSTINIL
0.2%
of all TREPROSTINIL reports
8
Deaths
58
Hospitalizations
How Dangerous Is Decreased activity From TREPROSTINIL?
Of the 195 reports, 8 (4.1%) resulted in death, 58 (29.7%) required hospitalization, and 2 (1.0%) were considered life-threatening.
Is Decreased activity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 195 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 Decreased activity?
NIRAPARIB (586)
SACUBITRIL\VALSARTAN (570)
RUXOLITINIB (558)
DUPILUMAB (231)
LEVOTHYROXINE (201)
PREDNISONE (193)
ALBUTEROL (190)
EMTRICITABINE\TENOFOVIR DISOPROXIL (186)
TERIPARATIDE (156)
EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL (145)
Which TREPROSTINIL Alternatives Have Lower Decreased activity Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE