Prescribing information

 

   

Pyrexia was the most common adverse event observed in Phase III clinical trials of Tafinlar (dabrafenib) + Mekinist (trametinib). This brochure is designed to provide guidance on how to monitor your patients for the onset of pyrexia and advises on how best to manage pyrexia to allow continued treatment with Tafinlar + Mekinist.

Images provided for illustrative purposes only.  Please contact your Novartis Representative to receive a copy of this brochure.

TMC20-C016b May 2020
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Adverse events should be reported. Reporting forms and information can be found at yellowcard.mhra.gov.uk. Adverse events should also be reported to Novartis via [email protected] or online through the patient safety information (PSI) tool at https://psi.novartis.com
If you have a question about the product, please contact Medical Information on 01276 692255 or by email at [email protected]