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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does RIBOCICLIB Cause Haematotoxicity? 129 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 129 reports of Haematotoxicity have been filed in association with RIBOCICLIB (KISQALI). This represents 0.5% of all adverse event reports for RIBOCICLIB.

129
Reports of Haematotoxicity with RIBOCICLIB
0.5%
of all RIBOCICLIB reports
7
Deaths
12
Hospitalizations

How Dangerous Is Haematotoxicity From RIBOCICLIB?

Of the 129 reports, 7 (5.4%) resulted in death, 12 (9.3%) required hospitalization, and 8 (6.2%) were considered life-threatening.

Is Haematotoxicity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIBOCICLIB. However, 129 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 Haematotoxicity?

CYCLOPHOSPHAMIDE (1,410) DOXORUBICIN (1,180) VINCRISTINE (1,038) RITUXIMAB (812) CARBOPLATIN (803) METHOTREXATE (799) PREDNISONE (730) CYTARABINE (701) ETOPOSIDE (677) CISPLATIN (668)

Which RIBOCICLIB Alternatives Have Lower Haematotoxicity Risk?

RIBOCICLIB vs RIBOFLAVIN RIBOCICLIB vs RIBOFLAVIN 5'-PHOSPHATE RIBOCICLIB vs RIBOFLAVIN 5^-PHOSPHATE RIBOCICLIB vs RIFABUTIN RIBOCICLIB vs RIFAMPICIN

Related Pages

RIBOCICLIB Full Profile All Haematotoxicity Reports All Drugs Causing Haematotoxicity RIBOCICLIB Demographics