Does BOSENTAN Cause Condition aggravated? 739 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 739 reports of Condition aggravated have been filed in association with BOSENTAN (Tracleer). This represents 3.8% of all adverse event reports for BOSENTAN.
739
Reports of Condition aggravated with BOSENTAN
3.8%
of all BOSENTAN reports
239
Deaths
464
Hospitalizations
How Dangerous Is Condition aggravated From BOSENTAN?
Of the 739 reports, 239 (32.3%) resulted in death, 464 (62.8%) required hospitalization, and 26 (3.5%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOSENTAN. However, 739 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which BOSENTAN Alternatives Have Lower Condition aggravated Risk?
BOSENTAN vs BOSENTAN\BOSENTAN
BOSENTAN vs BOSUTINIB
BOSENTAN vs BOTOX
BOSENTAN vs BOTOX COSMETIC
BOSENTAN vs BOTULINUM TOXIN NOS