Kisqali Femara Co-pack Generic Name & Formulations
Ribociclib 200mg; with letrozole 2.5mg; tabs.
Kinase inhibitor + aromatase inhibitor.
Cartons—28 days of therapy (63 tabs x 200mg + 28 tabs); (42 tabs x 200mg + 28 tabs); (21 tabs x 200mg + 28 tabs)
Kisqali Femara Co-pack Indications
Initial endocrine-based therapy for the treatment of pre/perimenopausal or postmenopausal women with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer.
Kisqali Femara Co-pack Dosage and Administration
Take together preferably in the AM. Swallow whole. Kisqali: initially 600mg once daily for 21 consecutive days, followed by 7 days off treatment for a complete 28-day cycle. Femara: 2.5mg once daily throughout the 28-day cycle. Pre/perimenopausal women: also treat with LHRH agonist. Concomitant strong CYP3A4 inhibitors: avoid; if coadmin necessary, reduce Kisqali to 400mg once daily. Hepatic impairment: reduce Kisqali to 400mg once daily (moderate and severe); Femara 2.5mg every other day (cirrhosis and severe dysfunction). Severe renal impairment: initially Kisqali 200mg once daily. Dose modifications for toxicity: see full labeling.
Kisqali Femara Co-pack Contraindications
Kisqali Femara Co-pack Boxed Warnings
Kisqali Femara Co-pack Warnings/Precautions
Monitor for interstitial lung disease (ILD)/pneumonitis; interrupt immediately and evaluate if suspected. Permanently discontinue if recurrent symptomatic or severe ILD/pneumonitis occurs. Risk of severe cutaneous adverse reactions (eg, SJS, TEN, DiHS/DRESS), QT interval prolongation. Permanently discontinue if SJS, TEN, or DiHS/DRESS is confirmed; do not reintroduce. Assess ECG prior to initiation; start therapy only if QTcF values <450 msec. Repeat ECG at Day 14 of Cycle 1, beginning of Cycle 2, and as clinically indicated; monitor more frequently if any QTcF prolongation occurs. Monitor serum electrolytes prior to initiation, at the beginning of the first 6 cycles, and as clinically indicated; correct any abnormality before starting. Avoid in patients with long QT syndrome, uncontrolled or significant cardiac disease including recent MI, CHF, unstable angina and bradyarrhythmias, electrolyte abnormalities. Perform LFTs prior to initiation; monitor every 2 weeks for first 2 cycles, at the beginning of each subsequent 4 cycles, and as clinically indicated; monitor more frequently if Grade ≥2 abnormalities noted. Perform CBC prior to initiation; monitor every 2 weeks for first 2 cycles, at the beginning of each subsequent 4 cycles, and as clinically indicated. Hepatic impairment. Severe renal impairment. Embryo-fetal toxicity. Pregnancy: exclude status prior to initiation. Advise females of reproductive potential to use effective contraception during and for ≥3 weeks after last dose. Nursing mothers: not recommended (during and for ≥3 weeks after last dose).
Kisqali Femara Co-pack Pharmacokinetics
Kisqali Femara Co-pack Interactions
Concomitant Kisqali with tamoxifen: not indicated. Avoid concomitant with strong CYP3A inhibitors (eg, boceprevir, clarithromycin, conivaptan, indinavir, itraconazole, ketoconazole, lopinavir/ritonavir, nefazodone, nelfinavir, posaconazole, ritonavir, saquinavir, voriconazole); consider alternatives or see Adult. Avoid grapefruit, grapefruit juice, pomegranates, pomegranate juice. Avoid concomitant with strong CYP3A inducers (eg, phenytoin, rifampin, carbamazepine, St. John’s wort); consider alternatives. Caution with concomitant CYP3A substrates with a narrow therapeutic index (eg, alfentanil, cyclosporine, ergots, everolimus, fentanyl, midazolam, pimozide, quinidine, sirolimus, tacrolimus); may need to reduce these doses. Avoid concomitant with drugs known to prolong QT interval (eg, amiodarone, bepridil, chloroquine, clarithromycin, disopyramide, halofantrine, haloperidol, methadone, moxifloxacin, ondansetron, pimozide, procainamide, quinidine, sotalol).
Kisqali Femara Co-pack Adverse Reactions
Neutropenia, nausea, infections, fatigue, diarrhea, leukopenia, alopecia, vomiting, constipation, headache, back pain, rash, anemia; hepatobiliary toxicity, lab abnormalities.
Kisqali Femara Co-pack Clinical Trials
Kisqali Femara Co-pack Note
Kisqali Femara Co-pack Patient Counseling