Does RIBOCICLIB Cause Product dose omission? 15 Reports in FDA Database

Q: Does RIBOCICLIB cause Product dose omission?

15 reports of Product dose omission have been filed with the FDA for RIBOCICLIB, representing 0.1% of all RIBOCICLIB adverse event reports.

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product dose omission have been filed in association with RIBOCICLIB (KISQALI). This represents 0.1% of all adverse event reports for RIBOCICLIB.

Reports of Product dose omission with RIBOCICLIB

0.1%

of all RIBOCICLIB reports

Deaths

Hospitalizations

How Dangerous Is Product dose omission From RIBOCICLIB?

Of the 15 reports, 6 (40.0%) required hospitalization.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIBOCICLIB. However, 15 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 Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which RIBOCICLIB Alternatives Have Lower Product dose omission Risk?

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

RIBOCICLIB Full Profile All Product dose omission Reports All Drugs Causing Product dose omission RIBOCICLIB Demographics