Does BOSENTAN Cause Product dose omission issue? 798 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 798 reports of Product dose omission issue have been filed in association with BOSENTAN (Tracleer). This represents 4.1% of all adverse event reports for BOSENTAN.
798
Reports of Product dose omission issue with BOSENTAN
4.1%
of all BOSENTAN reports
18
Deaths
174
Hospitalizations
How Dangerous Is Product dose omission issue From BOSENTAN?
Of the 798 reports, 18 (2.3%) resulted in death, 174 (21.8%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOSENTAN. However, 798 reports have been filed with the FAERS database.
What Other Side Effects Does BOSENTAN Cause?
Dyspnoea (2,492)
Death (2,388)
Pneumonia (1,064)
Fatigue (1,025)
Headache (962)
Hospitalisation (915)
Malaise (894)
Diarrhoea (840)
Pulmonary arterial hypertension (778)
Nausea (765)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which BOSENTAN Alternatives Have Lower Product dose omission issue Risk?
BOSENTAN vs BOSENTAN\BOSENTAN
BOSENTAN vs BOSUTINIB
BOSENTAN vs BOTOX
BOSENTAN vs BOTOX COSMETIC
BOSENTAN vs BOTULINUM TOXIN NOS