Does AMBRISENTAN Cause Product dose omission? 413 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 413 reports of Product dose omission have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.5% of all adverse event reports for AMBRISENTAN.
413
Reports of Product dose omission with AMBRISENTAN
0.5%
of all AMBRISENTAN reports
13
Deaths
217
Hospitalizations
How Dangerous Is Product dose omission From AMBRISENTAN?
Of the 413 reports, 13 (3.1%) resulted in death, 217 (52.5%) required hospitalization, and 3 (0.7%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 413 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which AMBRISENTAN Alternatives Have Lower Product dose omission Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE