Does AMBRISENTAN Cause Unevaluable event? 2,336 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,336 reports of Unevaluable event have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 2.7% of all adverse event reports for AMBRISENTAN.
2,336
Reports of Unevaluable event with AMBRISENTAN
2.7%
of all AMBRISENTAN reports
111
Deaths
1,107
Hospitalizations
How Dangerous Is Unevaluable event From AMBRISENTAN?
Of the 2,336 reports, 111 (4.8%) resulted in death, 1,107 (47.4%) required hospitalization, and 9 (0.4%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 2,336 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
HYDROMORPHONE (1,118)
Which AMBRISENTAN Alternatives Have Lower Unevaluable event Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE