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Amyvid

"Today, the U.S. Food and Drug Administration issued a proposal designed to assist companies developing new treatments for patients in the early stages of Alzheimer's disease, before the onset of noticeable (overt) dementia.

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Amyvid

PATIENT INFORMATION

  • Instruct patients to inform their physician or healthcare provider if they are pregnant or breastfeeding.
  • Inform patients who are breastfeeding to use alternate infant nutrition sources (e.g., stored breast milk or infant formula) for 24 hours ( > 10 half-lives of radioactive decay for the F 18 isotope) after administration of the drug or avoid use of the drug.

Last reviewed on RxList: 1/23/2014
This monograph has been modified to include the generic and brand name in many instances.

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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