Does AMBRISENTAN Cause Haemoglobin decreased? 619 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 619 reports of Haemoglobin decreased have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.7% of all adverse event reports for AMBRISENTAN.
619
Reports of Haemoglobin decreased with AMBRISENTAN
0.7%
of all AMBRISENTAN reports
22
Deaths
407
Hospitalizations
How Dangerous Is Haemoglobin decreased From AMBRISENTAN?
Of the 619 reports, 22 (3.6%) resulted in death, 407 (65.8%) required hospitalization, and 6 (1.0%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 619 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which AMBRISENTAN Alternatives Have Lower Haemoglobin decreased Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE