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IMBRUVICA® (ibrutinib) U S Prescribing Information Updated to Include Long-Term Data for Waldenström s Macroglobulinemia (WM)
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Top 10 Gastroenterology Articles Provide Essential Guidance
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ABBVie announced today that the U.S. Food and Drug Administration approved the update of the IMBRUVICA ® Prescribing Information to include efficacy and safety data for the combination of IMBRUVICA with rituximab for the treatment of Waldenström’s macroglobulinemia based on the final analysis of the Phase 3 iNNOVATE study. First approved in 2013, IMBRUVICA is currently available to patients with several types of …
– ABBVie (NYSE: ABBV) announced today that the U.S. Food and Drug Administration (FDA) approved the update of the IMBRUVICA ® (ibrutinib) Prescribing Information to include efficacy and safety data for the combination of IMBRUVICA with rituximab for the treatment of Waldenström’s macroglobulinemia (WM), based on the final analysis of the Phase 3 iNNOVATE study. First approved in 2013, IMBRUVICA is currently available to patients with several types of blood cancer, as well as chronic graft-versus-host disease. It was approved as a monotherapy for WM in 2015 and
Brief clinical appointments are making it impossible for women with breast cancer to get vital information about issues like whether to have a mastectomy or not, a researcher says.
A researcher says informed consent on surgical procedures like a mastectomy may be illusory due to lack of meaningful consultation.
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The claim, by a doctorate researcher in Taranaki, adds to the controversy around informed consent, and whether the principle is being applied meaningfully and legally in the country s hospitals. Informed decision-making may be only an illusion, said Mary Sylvester, a veteran nurse now researching with AUT into breast cancer treatment.
Verification that safety-critical elements are suitable and effective at a major hazard facility or petroleum installation
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