Does AMBRISENTAN Cause Device dislocation? 255 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 255 reports of Device dislocation have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.3% of all adverse event reports for AMBRISENTAN.
255
Reports of Device dislocation with AMBRISENTAN
0.3%
of all AMBRISENTAN reports
8
Deaths
157
Hospitalizations
How Dangerous Is Device dislocation From AMBRISENTAN?
Of the 255 reports, 8 (3.1%) resulted in death, 157 (61.6%) required hospitalization, and 1 (0.4%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 255 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 dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which AMBRISENTAN Alternatives Have Lower Device dislocation Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE