Vemurafenib-induced bilateral facial palsy

The United States Food and Drug Administration (FDA) approved Vemurafenib in August 2011, for treatment of melanoma with BRAF V600 mutation. It has shown improvement in the median overall survival of melanoma patients. The most common adverse effects of vermurafenib are arthralgia, rash, alopecia, p...

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Bibliographic Details
Main Authors: FNU Shailesh, M Singh, U Tiwari, L F Hutchins
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:Journal of Postgraduate Medicine
Subjects:
Online Access:http://www.jpgmonline.com/article.asp?issn=0022-3859;year=2014;volume=60;issue=2;spage=187;epage=188;aulast=Shailesh