Does TREPROSTINIL Cause Haemoglobin increased? 245 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 245 reports of Haemoglobin increased have been filed in association with TREPROSTINIL (TYVASO). This represents 0.3% of all adverse event reports for TREPROSTINIL.
245
Reports of Haemoglobin increased with TREPROSTINIL
0.3%
of all TREPROSTINIL reports
3
Deaths
30
Hospitalizations
How Dangerous Is Haemoglobin increased From TREPROSTINIL?
Of the 245 reports, 3 (1.2%) resulted in death, 30 (12.2%) required hospitalization.
Is Haemoglobin increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 245 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 Haemoglobin increased?
RUXOLITINIB (332)
SOTATERCEPT (151)
CLOZAPINE (142)
SOTATERCEPT-CSRK (100)
DARBEPOETIN ALFA (99)
TESTOSTERONE (96)
METFORMIN (93)
VOXELOTOR (86)
ROSUVASTATIN (85)
ADALIMUMAB (81)
Which TREPROSTINIL Alternatives Have Lower Haemoglobin increased Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE