Primodos: the MHRA launches a public call for evidence relating to its use

Hormonal pregnancy tests: call for evidence relating to Primodos use.

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Primodos: UK Medicines regulator launches call for evidence on previously licensed oral hormonal pregnancy tests.

Public call for evidence launched relating to the use of hormonal contraceptives

The Medicines and Healthcare products Regulatory Agency (MHRA) has today launched a public call for evidence relating to the use of oral hormonal pregnancy tests (HPTs, which are no longer prescribed in the UK) and adverse effects relating to pregnancy including possible birth defects.

HPTs such as Primodos were available in the 1960s and 1970s and were widely used to diagnose pregnancy. In 1967, a study raised initial concern that use of HPTs may be associated with birth defects. The then Committee on Safety of Medicines (CSM) kept this issue under review and in 1975 recommended that in view of the possible concern, and the availability of alternative methods, doctors should not use HPTs. These products were withdrawn from the market in the late 1970s.

In October 2014, the government committed to an independent review of the evidence relating to HPTs and the possible risk of birth defects. The review is not a political inquiry intended to demonstrate liability, but to examine the evidence to assess whether there are grounds for accepting a link between the use of HPTs and the conditions experienced by some patients.

A group of experts in relevant scientific disciplines is currently being convened to conduct the review, which is expected to be completed by the beginning of 2016.

To ensure all the available evidence is reviewed, the MHRA is currently in the process of obtaining all relevant documents. As part of this process, the MHRA is asking any individual or organisation with information they feel is relevant to submit it for consideration by the experts during the review. All evidence submitted will be included in the review and a report (including a public summary) will be made publicly available once the review is complete.

Dr June Raine, the MHRA’s Director of Vigilance and Risk Management of Medicines, said:

We encourage people to send us any information they consider is relevant to previously used hormonal pregnancy tests and potential adverse effects that they think may have been associated with these drugs.

“It is important that we hear from people who feel they or their child have been affected adversely by hormonal pregnancy tests. We encourage anyone who wants to provide information about a suspected adverse effect from use of a HPT to submit it to us via a Yellow Card report.

“We would also welcome any other published or unpublished evidence you consider relevant and wish to submit for the review and ask that you send this to us by the end of June 2015. ”

Sources
  • Medicines regulator launches call for evidence on previously licensed oral hormonal pregnancy tests, MHRA press release, 25 March 2015.
  • Hormonal pregnancy tests: call for evidence, MHRA Consultation description, 25 March 2015.
  • Hormonal pregnancy tests (including Primodos) and possible association with birth defects, MHRA Call for evidence, 25 March 2015.

More about Primodos

Author: DES Daughter

Activist, blogger and social media addict committed to shedding light on a global health scandal and dedicated to raise DES awareness.

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