Does TREPROSTINIL Cause Recalled product administered? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Recalled product administered have been filed in association with TREPROSTINIL (TYVASO). This represents 0.0% of all adverse event reports for TREPROSTINIL.
19
Reports of Recalled product administered with TREPROSTINIL
0.0%
of all TREPROSTINIL reports
1
Deaths
2
Hospitalizations
How Dangerous Is Recalled product administered From TREPROSTINIL?
Of the 19 reports, 1 (5.3%) resulted in death, 2 (10.5%) required hospitalization.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 19 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which TREPROSTINIL Alternatives Have Lower Recalled product administered Risk?
TREPROSTINIL vs TREPROSTINIL DIOLAMINE
TREPROSTINIL vs TRETINOIN
TREPROSTINIL vs TRIAMCINOLONE
TREPROSTINIL vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE