Does AMBRISENTAN Cause Wrong technique in product usage process? 201 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 201 reports of Wrong technique in product usage process have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.2% of all adverse event reports for AMBRISENTAN.
201
Reports of Wrong technique in product usage process with AMBRISENTAN
0.2%
of all AMBRISENTAN reports
16
Deaths
72
Hospitalizations
How Dangerous Is Wrong technique in product usage process From AMBRISENTAN?
Of the 201 reports, 16 (8.0%) resulted in death, 72 (35.8%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 201 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which AMBRISENTAN Alternatives Have Lower Wrong technique in product usage process Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE