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  2. Antiestrogen withdrawal response - Wikipedia

    en.wikipedia.org/wiki/Antiestrogen_withdrawal...

    The antiestrogen withdrawal response is a paradoxical improvement in breast cancer caused by discontinuation of antiestrogen therapy for breast cancer. [1] [2] [3] [4 ...

  3. Tamoxifen - Wikipedia

    en.wikipedia.org/wiki/Tamoxifen

    Tamoxifen was initially made in 1962, by chemist Dora Richardson. [17] [18] It is on the World Health Organization's List of Essential Medicines. [19] Tamoxifen is available as a generic medication. [14] In 2020, it was the 317th most commonly prescribed medication in the United States, with more than 900 thousand prescriptions. [20] [21]

  4. Selective estrogen receptor modulator - Wikipedia

    en.wikipedia.org/wiki/Selective_estrogen...

    Tamoxifen is a pure antiestrogenic trans-isomer and has differential actions at estrogen target tissues throughout the body. Tamoxifen is selectively antiestrogenic in the breast but estrogen-like in bones and endometrial cancer. [24] Tamoxifen undergo phase I metabolism in the liver by microsomal cytochrome P450 (CYP) enzymes.

  5. Danielle Fishel Says 20 Rounds of Radiation Left Her with a ...

    www.aol.com/lifestyle/danielle-fishel-says-20...

    She shared that she will start on the hormone therapy Tamoxifen once she recovers from the radiation. “They didn't wanna overload me with negative side effects,” Fishel said, adding that ...

  6. 5 Uses for DHEA Supplements for Men, From Depression to ...

    www.aol.com/5-benefits-dhea-supplements-men...

    Tamoxifen. Triazolam. Estrogens. Testosterone. You should also watch out for herbal supplements that might slow blood clotting, such as garlic, ginger, ginkgo, licorice, nattokinase and Panax ginseng.

  7. N-Desmethyltamoxifen - Wikipedia

    en.wikipedia.org/wiki/N-Desmethyltamoxifen

    N-Desmethyltamoxifen (developmental code name ICI-55,548) is a major metabolite of tamoxifen, a selective estrogen receptor modulator (SERM). [1] [2] N-Desmethyltamoxifen is further metabolized into endoxifen (4-hydroxy-N-desmethyltamoxifen), which is thought to be the major active form of tamoxifen in the body.