You are here

Miraculous Evil Root tablets

Safety advisory

24 January 2012

The supply of Miraculous Evil Root tablets in Australia is illegal. However, a number of people in Australia have bought the product online.

The Therapeutic Goods Administration (TGA) has tested Miraculous Evil Root tablets and found that:

  • it contains the undeclared prescription substance sildenafil (the active ingredient in Viagra) - this is despite the claim made on the box that it is a pure natural product.
  • the levels of sildenafil the tablets contain are higher than the levels approved by the TGA for prescription sildenafil.

Information for consumers

Miraculous Evil Root boxTaking Evil Root tablets poses a serious risk to your health.

  • Stop taking Miraculous Evil Root tablets and discard any remaining tablets.
  • If you have any concerns arising from your use of this product, consult your health care practitioner.

Miraculous Evil Root tablets have not been assessed by the TGA for quality, safety or efficacy as required under Australian legislation, and the place of manufacture is not approved by the TGA.

Action the TGA is taking

Miraculous Evil Root bottleThe TGA is working with Australian Customs and Border Protection Services (Customs) to help stop future shipments of Miraculous Evil Root tablets from entering Australia.

If these tablets are found at the border by Customs they will be seized and destroyed.

The TGA is advising consumers to exercise extreme caution when purchasing medicines from unknown overseas Internet sites. 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:

online: Report a perceived breach of the Therapeutic Goods Act or questionable practices relating to therapeutic products

in writing, via post to:
Chief Investigator
Regulatory Compliance Unit
Therapeutic Goods Administration
PO Box 100
Woden ACT 2606