Dabrafenib package insert

Package insert. Hospira; 2024. 19. Cefazolin. Package insert. GSK; 2024. 20. Ceftriaxone. Package insert. Sandoz; 2024. 21. Daptomycin. Package insert

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A. Please refer to the FDA label/package insert for details regarding these topics. V. APPROVAL AUTHORITY A. Review – Utilization Management Department B. Final Approval – Utilization Management Committee VI. ATTACHMENTS A. None VII. REFERENCES A. Long GV, et al. COMBI-d Clinical Trial. Dabrafenib plus trametinib versus dabrafenib

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Fever in patients receiving dabrafenib should not be immediately assumed to be drug-related; rather, fever should first prompt a consideration of infectious causes. The dabrafenib package insert offers vague management guidelines for fever, and little information on fever management in dabrafenib-treated patients has been published.

Dabrafenib can be used as a single agent to treat melanoma with the BRAF valine 600 to glutamic acid (V600E) variant or in combination with the MEK inhibitor trametinib to treat multiple tumor types with BRAF V600E or V600K variants. (1) TAFINLAR- dabrafenib capsule [package insert]. East Hanover, NJ: Corporation, N.P.; 2025.

The Food and Drug Administration (FDA) has approved Tafinlar (dabrafenib) with Mekinist Tafinlar. Package insert. Novartis; 2025. Accessed Ma.

The educational content on WikiDoc drug pages is based upon the FDA package insert, National Library of Medicine content and practice guidelines / consensus statements. Dabrafenib mesylate is a BRAF Inhibitor that is FDA approved

Dabrafenib (Tafinlar) package insert; Dabrafenib (Tafinlar) patient drug information (Chemocare) History of changes in FDA indication Low-grade glioma, pediatric. : FDA approved for pediatric patients 1 year of age and older with low-grade glioma (LGG) with a BRAF V600E mutation who require systemic therapy.