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Beefit capsules
Safety advisory
Published
The Therapeutic Goods Administration (TGA) has tested a product labelled BEEFIT capsules and found that:
- the capsules contain the undeclared substance sibutramine.
- consumers are advised that sibutramine is a prescription-only medicine (which was the active ingredient in Reductil). It was withdrawn in October 2010 after a study showed an increased risk of major cardiac events.
Information for consumers
- Stop taking Beefit capsules and take any remaining capsules to your local pharmacy for safe disposal.
- If you have any concerns arising from your use of this product, consult your health care practitioner.
Action the TGA is taking
The TGA is working with the Australian Border Force (ABF) to help stop future shipments of Beefit capsules from entering Australia.
If these capsules are found at the border by the ABF they will be seized and destroyed.
The TGA is advising consumers to exercise extreme caution when purchasing medicines from unknown overseas Internet sites and has produced a short video on the risks associated with buying medicines and medical devices online. Products purchased over the Internet:
- may contain undisclosed and potentially harmful ingredients
- may not meet the same standards of quality, safety and efficacy as those approved by the TGA for supply in Australia.
Report counterfeit medicines and medical devices
If you are worried about counterfeit medicines or medical devices, and want to report an issue, you can report the matter to the TGA:
- Phone: 1800 020 653
- Online: Report a perceived breach of the Therapeutic Goods Act or questionable practices relating to therapeutic products
- Email: info@tga.gov.au
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