Ibrance Generic Name & Formulations
Legal Class
General Description
Pharmacological Class
How Supplied
Manufacturer
Generic Availability
Mechanism of Action
Ibrance Indications
Indications
Ibrance Dosage and Administration
Adult
Children
Ibrance Contraindications
Not Applicable
Ibrance Boxed Warnings
Not Applicable
Ibrance Warnings/Precautions
Warnings/Precautions
Monitor CBCs prior to initiation and at start of each cycle, as well as on Day 15 of first 2 cycles, and as clinically indicated. Interrupt, reduce dose, or delay starting treatment cycles if Grade 3 or 4 neutropenia develops. If maximum of Grade 1–2 neutropenia develops in first 6 cycles, monitor CBCs for subsequent cycles every 3 months, at start of each cycle, and as clinically indicated. Monitor for interstitial lung disease (ILD)/pneumonitis; interrupt immediately if suspected. Permanently discontinue if severe ILD/pneumonitis occurs. Severe hepatic impairment. Hemodialysis. Embryo-fetal toxicity. Advise use of effective contraception during and for at least 3 weeks (females of reproductive potential) or 3 months (males w. female partners) after the last dose. Pregnancy: exclude status prior to initiation. Nursing mothers: not recommended (during and for 3 weeks after the last dose).
Ibrance Pharmacokinetics
Distribution
Mean apparent volume of distribution: 2583 L. Plasma protein bound: ~85%.
Elimination
Fecal (74.1%), renal (17.5%). Half-life: 29 hours. Mean apparent oral clearance: 63.1 L/hr.
Ibrance Interactions
Interactions
Ibrance Adverse Reactions
Adverse Reactions
Ibrance Clinical Trials
See Literature
Ibrance Note
Not Applicable
Ibrance Patient Counseling
See Literature
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