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I have been on Capecitabine since 2010 and haven't had any side effects with this medication. I was diagnosed with breast cancer in 2009 and since that time have tried many medications and undergone two chemotherapies. I believe it's due to Capecitabine that I haven't lost my hair and had no complications after the chemotherapies. In general I have wonderful results without side effects. I am now 41, the cancer seems to have stepped aside and I am looking forward to many more years of continued good health.

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The study met its primary objective of improving PFS in the second-line, significantly reducing the risk of tumour progression by 25 percent with the addition of Avastin to chemotherapy compared to chemotherapy alone in women with HER2-negative metastatic breast cancer.

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Hands have never been a problem, feet are dry cracked and sometimes sore, wearing socks helps alot!

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HER2-negative breast cancer and did not have a pathologic complete response to neoadjuvant chemotherapy, you might want to talk to your doctor about this study, especially if the cancer was large or involved more than one or two lymph nodes.

Short of forgetting that she already told you the same story twice now, or the occasional forgetting what something is called, my Mom lucked out with this side effect.

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In patients with mild to moderate hepatic dysfunction due to liver metastases, no starting dose adjustment is necessary; however, patients should be carefully monitored.

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Your doctor may prescribe other medicines for these side effects.

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The Institute of Medicine, a nonprofit organization that gives expert advice on health, recommends that adults age 19 to 70 get 600 IU a day.

As well as its needed effects, capecitabine (the active ingredient contained in Xeloda) may cause unwanted side effects that require medical attention.

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Three cases of severe angina-like chest pain possibly or probably related to capecitabine (the active ingredient contained in Xeloda) treatment have been reported.

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Capecitabine is an oral prodrug that is converted to its only active metabolite, FU, by thymidine phosphorylase.

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Treatment may be resumed during the cycle at 50% of the original XELODA dose.

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Improvement of systemic symptoms (eg, headache, lethargy) typically occurs within 72 hours of initiation of therapy.

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