The black box warning was just one of several moves the FDA announced regarding the products. The Food and Drug Administration (FDA or USFDA) is an agency of the United States Department of Health and Human Services and is responsible for regulating and supervising the safety of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics.
The manufacturers will also be required to:
- Inform users in writing about the potential risk for distant spread at the time of injection.
- Warn doctors and patients about the risks associated with substituting one botulism product for another. The products have different dosing units, which are incompatible, so switching products can result in dangerous overdosing.
- Follow a group of children and adults using Botox, Myobloc, or Dysport off-label to treat involuntary muscle movement and submit safety data to the agency.
Read more about BOTOX warnings on >>>>
http://www.webmd.com/skin-problems-and-treatments/news/20090430/black-box-warning-for-botox
Do we have any such type of regulation in
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