FDA Adds Black Box Warning to Nolvadex
June 27, 2002
The U.S. Food and Drug Administration (FDA) and AstraZeneca Pharmaceuticals LP have added a boxed warning and strengthened the WARNINGS section of the label for Tamoxifen Citrate, sold under the brand name Nolvadex. The warning informs healthcare professionals about new risk information of particular relevance to women with ductal carcinoma in situ [DCIS] and women at high risk for developing breast cancer who are receiving or considering Nolvadex therapy to reduce their risk of developing invasive breast cancer.
Serious, life-threatening or fatal events associated with Nolvadex in the risk reduction setting [women at high risk for cancer and women with DCIS] include endometrial cancer, uterine sarcoma, stroke, and pulmonary embolism. Healthcare providers should discuss the potential benefits versus the potential risks of these serious events with women considering Nolvadex to reduce their risk of developing breast cancer.
-- Article Courtesy of InjuryBoard.com
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