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FDA Approves Pomalyst for Advanced Multiple Myeloma »
"The U.S. Food and Drug Administration today approved Pomalyst (pomalidomide) to treat patients with multiple myeloma whose disease progressed after being treated with other cancer drugs.
Multiple myeloma is a form of blood cancer that p"...
Read the FDA Approves Pomalyst for Advanced Multiple Myeloma article »
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Some products that may interact with this drug include: dimethylsulfoxide (DMSO) products applied to the skin, natalizumab.
OVERDOSE: If overdose is suspected, contact a poison control center or emergency room immediately. US residents can call the US National Poison Hotline at 1-800-222-1222. Canada residents can call a provincial poison control center.
NOTES: Keep all medical appointments while using this medication. Laboratory and/or medical tests (such as complete blood counts, examination of the injection site) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.
MISSED DOSE: For the best possible benefit, it is important to receive each scheduled dose of this medication as directed. If you miss a dose, contact your doctor or pharmacist immediately to establish a new dosing schedule.
STORAGE: Not applicable. This medication is given in a clinic and will not be stored at home.
Information last revised March 2012. Copyright(c) 2012 First Databank, Inc.
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