European Medicines Agency sees no safety concerns with the Rotarix oral vaccine

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Press release

26/03/2010

European Medicines Agency sees no safety concerns with the Rotarix oral vaccine

The European Medicines Agency has concluded that the unexpected presence of DNA of a non-disease causing viral strain in batches of the oral vaccine Rotarix does not present a risk to public health. At an extraordinary meeting held on 25 March 2010, the Committee for Medicinal Products for Human Use (CHMP) endorsed the recommendations from its Vaccines Working Party and agreed that there was no need to restrict the use of Rotarix

Rotarix is a vaccine given by mouth to children of 6 weeks and older, to protect against gastroenteritis (diarrhoea and vomiting) due to rotavirus infection.

The DNA found in the vaccine matches that of porcine circovirus type 1 (PCV1). This virus is commonly found in certain meat and other food products, and is not known to cause disease in either animals or humans. The DNA has not been found in other live attenuated vaccines from the same manufacturer, GSK Biologicals.

However, viral DNA should not be present in the Rotarix vaccine and its source is unclear. The Committee has therefore requested that the manufacturer identifies the root cause of the finding and introduces measures to manufacture the vaccine free of PCV1 DNA.

The CHMP will be reviewing all new data on an ongoing basis. The Committee will consider the need for further recommendations in its meetings in April and May 2010, as further data emerges.

Name Language First published Last updated
European Medicines Agency sees no safety concerns with the Rotarix oral vaccine (English only) 2010-03-26  

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Contact point:

Martin Harvey Allchurch or Monika Benstetter
Tel. +44 (0)20 7418 8427
E-mail: press@ema.europa.eu