Does AMBRISENTAN Cause Device breakage? 79 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Device breakage have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.1% of all adverse event reports for AMBRISENTAN.
79
Reports of Device breakage with AMBRISENTAN
0.1%
of all AMBRISENTAN reports
3
Deaths
63
Hospitalizations
How Dangerous Is Device breakage From AMBRISENTAN?
Of the 79 reports, 3 (3.8%) resulted in death, 63 (79.7%) required hospitalization, and 1 (1.3%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 79 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 breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which AMBRISENTAN Alternatives Have Lower Device breakage Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE