Does RIBOCICLIB Cause Haemoglobin decreased? 709 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 709 reports of Haemoglobin decreased have been filed in association with RIBOCICLIB (KISQALI). This represents 2.5% of all adverse event reports for RIBOCICLIB.
709
Reports of Haemoglobin decreased with RIBOCICLIB
2.5%
of all RIBOCICLIB reports
132
Deaths
311
Hospitalizations
How Dangerous Is Haemoglobin decreased From RIBOCICLIB?
Of the 709 reports, 132 (18.6%) resulted in death, 311 (43.9%) required hospitalization, and 106 (15.0%) 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 RIBOCICLIB. However, 709 reports have been filed with the FAERS database.
What Other Side Effects Does RIBOCICLIB Cause?
Neutropenia (3,585)
Nausea (3,404)
Fatigue (3,327)
Malignant neoplasm progression (2,468)
Death (2,452)
Vomiting (1,953)
Diarrhoea (1,830)
White blood cell count decreased (1,683)
Pain (1,637)
Metastases to bone (1,538)
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 RIBOCICLIB Alternatives Have Lower Haemoglobin decreased Risk?
RIBOCICLIB vs RIBOFLAVIN
RIBOCICLIB vs RIBOFLAVIN 5'-PHOSPHATE
RIBOCICLIB vs RIBOFLAVIN 5^-PHOSPHATE
RIBOCICLIB vs RIFABUTIN
RIBOCICLIB vs RIFAMPICIN