Does EVEROLIMUS Cause Haemoglobin decreased? 602 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 602 reports of Haemoglobin decreased have been filed in association with EVEROLIMUS (EVEROLIMUS). This represents 1.5% of all adverse event reports for EVEROLIMUS.
602
Reports of Haemoglobin decreased with EVEROLIMUS
1.5%
of all EVEROLIMUS reports
141
Deaths
358
Hospitalizations
How Dangerous Is Haemoglobin decreased From EVEROLIMUS?
Of the 602 reports, 141 (23.4%) resulted in death, 358 (59.5%) required hospitalization, and 60 (10.0%) 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 EVEROLIMUS. However, 602 reports have been filed with the FAERS database.
What Other Side Effects Does EVEROLIMUS Cause?
Death (5,090)
Malignant neoplasm progression (3,789)
Diarrhoea (3,061)
Fatigue (2,946)
Stomatitis (2,692)
Nausea (2,079)
Dyspnoea (1,925)
Drug ineffective (1,837)
Pyrexia (1,664)
Decreased appetite (1,633)
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 EVEROLIMUS Alternatives Have Lower Haemoglobin decreased Risk?
EVEROLIMUS vs EVOLOCUMAB
EVEROLIMUS vs EXELON
EVEROLIMUS vs EXEMESTANE
EVEROLIMUS vs EXENATIDE
EVEROLIMUS vs EXFORGE