"The U.S. Food and Drug Administration today granted accelerated approval to Perjeta (pertuzumab) as part of a complete treatment regimen for patients with early stage breast cancer before surgery (neoadjuvant setting). Perjeta is the first FDA-ap"...
There is no experience with overdosage in human clinical trials. Single doses higher than 8 mg/kg have not been tested.
Last reviewed on RxList: 5/14/2015
This monograph has been modified to include the generic and brand name in many instances.
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