Does BOSENTAN Cause Product dose omission? 361 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 361 reports of Product dose omission have been filed in association with BOSENTAN (Tracleer). This represents 1.8% of all adverse event reports for BOSENTAN.
361
Reports of Product dose omission with BOSENTAN
1.8%
of all BOSENTAN reports
37
Deaths
168
Hospitalizations
How Dangerous Is Product dose omission From BOSENTAN?
Of the 361 reports, 37 (10.2%) resulted in death, 168 (46.5%) required hospitalization, and 6 (1.7%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOSENTAN. However, 361 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)
Product dose omission issue (798)
Pulmonary arterial hypertension (778)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which BOSENTAN Alternatives Have Lower Product dose omission Risk?
BOSENTAN vs BOSENTAN\BOSENTAN
BOSENTAN vs BOSUTINIB
BOSENTAN vs BOTOX
BOSENTAN vs BOTOX COSMETIC
BOSENTAN vs BOTULINUM TOXIN NOS