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The US Oncology Network Affiliated Physicians at Forefront of Cutting-Edge Prostate Cancer Treatment
Date:9/30/2011

na-Asheville

-Cancer Centers of the Carolinas-Comprehensive Cancer Care-St. Louis

-Comprehensive Cancer Centers of Nevada-Minnesota Oncology

-Northwest Cancer Specialists-Ocala Oncology Center

-Regional Cancer Care-Texas Oncology

-Virginia Cancer Specialists-Virginia Oncology Associates

-Wilshire Oncology Medical Group-Willamette Valley Cancer Institute and Research CenterPROVENGE Safety PROVENGE is intended solely for autologous use and is not routinely tested for transmissible infectious diseases.

In controlled clinical trials, serious adverse events reported in the PROVENGE group included acute infusion reactions (occurring within 1 day of infusion) and cerebrovascular events.  Severe (Grade 3) acute infusion reactions were reported in 3.5% of patients in the PROVENGE group.  Reactions included chills, fever, fatigue, asthenia, dyspnea, hypoxia, bronchospasm, dizziness, headache, hypertension, muscle ache, nausea, and vomiting. No Grade 4 or 5 acute infusion reactions were reported in patients in the PROVENGE group.

The most common adverse events (incidence ≥15%) reported in the PROVENGE group are chills, fatigue, fever, back pain, nausea, joint ache, and headache.

Please see full Prescribing Information for PROVENGE at www.provenge.com.

About Prostate CancerAccording to the American Cancer Society, prostate cancer is the most common non-sk
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SOURCE The US Oncology Network
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