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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BOSENTAN Cause Device malfunction? 32 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Device malfunction have been filed in association with BOSENTAN (Tracleer). This represents 0.2% of all adverse event reports for BOSENTAN.

32
Reports of Device malfunction with BOSENTAN
0.2%
of all BOSENTAN reports
9
Deaths
29
Hospitalizations

How Dangerous Is Device malfunction From BOSENTAN?

Of the 32 reports, 9 (28.1%) resulted in death, 29 (90.6%) required hospitalization, and 1 (3.1%) were considered life-threatening.

Is Device malfunction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BOSENTAN. However, 32 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 Device malfunction?

PEGFILGRASTIM (6,818) EXENATIDE (3,273) BUDESONIDE\FORMOTEROL (2,771) ABATACEPT (2,459) SOMATROPIN (2,311) GOLIMUMAB (2,293) SECUKINUMAB (2,259) ALBUTEROL (2,257) GUSELKUMAB (1,410) MOMETASONE FUROATE (1,332)

Which BOSENTAN Alternatives Have Lower Device malfunction Risk?

BOSENTAN vs BOSENTAN\BOSENTAN BOSENTAN vs BOSUTINIB BOSENTAN vs BOTOX BOSENTAN vs BOTOX COSMETIC BOSENTAN vs BOTULINUM TOXIN NOS

Related Pages

BOSENTAN Full Profile All Device malfunction Reports All Drugs Causing Device malfunction BOSENTAN Demographics