Diethylstilbestrol

(asked on 7th April 2025) - View Source

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 26 March 2025 to Question 38407 on Diethylstilbestrol, whether he plans to issue an apology to women who (a) experienced long-term health impacts, (b) were compelled to place their children up adoption and (c) experienced poor maternity care due to being prescribed Diethylstilbestrol between 1950 and 1980.


Answered by
Karin Smyth Portrait
Karin Smyth
Minister of State (Department of Health and Social Care)
This question was answered on 19th May 2025

The government took action regarding Diethylstilbestrol (DES) in the early 1970s. In 1971, it was recognised that DES could cause a distinct type of cancer in the daughters of women who took DES in early pregnancy. Shortly afterwards, its use was contraindicated in pregnancy, pre-menopausal women, children and young adults and the Committee on Safety of Medicines wrote to all doctors in May 1973 to advise against the use of DES in pregnancy and pre-menopausal women.

Since 1992, the National Cancer Institute (NCI) at the US National Institutes of Health has been conducting the DES Follow-up Study of more than 21,000 mothers, daughters, and sons, exposed in the womb during the mother’s pregnancy, to better understand the long-term health effects of exposure to DES. The findings of this study have been published in the scientific literature.

As such, work has been undertaken to contact historic users of DES. Our sympathies are with anyone harmed by its historic use.

The UK Health Security Agency advises that routine cervical screening is appropriate for those who believe they were exposed to DES in utero. Further information is available at the following link:

https://www.gov.uk/government/publications/cervical-screening-programme-and-colposcopy-management/5-screening-and-management-of-immunosuppressed-individuals

Participation in the National Breast Screening Programme is also recommended. Pregnant women who know that they were exposed in utero to DES should inform their obstetrician and be aware of the increased risks of ectopic pregnancy and preterm labour.

The MHRA continuously assesses the benefit risk balance of all medicines at the time of initial licensing and throughout their use in clinical practice, carefully evaluating any emerging evidence on their benefits and risks.

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