Does AMBRISENTAN Cause Intentional dose omission? 595 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 595 reports of Intentional dose omission have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.7% of all adverse event reports for AMBRISENTAN.
595
Reports of Intentional dose omission with AMBRISENTAN
0.7%
of all AMBRISENTAN reports
27
Deaths
380
Hospitalizations
How Dangerous Is Intentional dose omission From AMBRISENTAN?
Of the 595 reports, 27 (4.5%) resulted in death, 380 (63.9%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 595 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
SOFOSBUVIR\VELPATASVIR (474)
Which AMBRISENTAN Alternatives Have Lower Intentional dose omission Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE