Does RIBOCICLIB Cause Full blood count abnormal? 90 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 90 reports of Full blood count abnormal have been filed in association with RIBOCICLIB (KISQALI). This represents 0.3% of all adverse event reports for RIBOCICLIB.
90
Reports of Full blood count abnormal with RIBOCICLIB
0.3%
of all RIBOCICLIB reports
13
Deaths
19
Hospitalizations
How Dangerous Is Full blood count abnormal From RIBOCICLIB?
Of the 90 reports, 13 (14.4%) resulted in death, 19 (21.1%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Full blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIBOCICLIB. However, 90 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 Full blood count abnormal?
ALBUTEROL (3,060)
PREDNISONE (2,230)
BUDESONIDE\FORMOTEROL (1,786)
TIOTROPIUM (1,754)
MONTELUKAST (1,529)
MEPOLIZUMAB (1,440)
BUDESONIDE (1,339)
PALBOCICLIB (1,146)
CICLESONIDE (916)
PANTOPRAZOLE (776)
Which RIBOCICLIB Alternatives Have Lower Full blood count abnormal Risk?
RIBOCICLIB vs RIBOFLAVIN
RIBOCICLIB vs RIBOFLAVIN 5'-PHOSPHATE
RIBOCICLIB vs RIBOFLAVIN 5^-PHOSPHATE
RIBOCICLIB vs RIFABUTIN
RIBOCICLIB vs RIFAMPICIN