Does AMBRISENTAN Cause Device malfunction? 91 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Device malfunction have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.1% of all adverse event reports for AMBRISENTAN.
91
Reports of Device malfunction with AMBRISENTAN
0.1%
of all AMBRISENTAN reports
7
Deaths
62
Hospitalizations
How Dangerous Is Device malfunction From AMBRISENTAN?
Of the 91 reports, 7 (7.7%) resulted in death, 62 (68.1%) required hospitalization, and 4 (4.4%) 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 AMBRISENTAN. However, 91 reports have been filed with the FAERS database.
What Other Side Effects Does AMBRISENTAN Cause?
Dyspnoea (13,367)
Death (7,497)
Headache (7,325)
Pneumonia (4,693)
Dizziness (4,561)
Fatigue (4,436)
Diarrhoea (4,312)
Nausea (3,986)
Fluid retention (3,927)
Malaise (3,839)
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 AMBRISENTAN Alternatives Have Lower Device malfunction Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE