Hormone Pregnancy Tests

Debate between Yasmin Qureshi and Mike Penning

Thursday 7th September 2023 Commons Chamber

[Yasmin Qureshi (Bolton South East) (Lab)]

I beg to move,

That this House notes that children were born with serious deformities due to the hormone pregnancy test drug Primodos, which was taken by expectant mothers between 1953 and 1975; further notes that official warnings were not issued about Primodos until eight years after the first reports indicated possible dangers; observes that the report by the Commission on Human Medicines’ Expert Working Group on Hormone Pregnancy Tests in 2017 was inconsistent with other academic reports; notes that the Independent Medicines and Medical Devices Safety Review, First do no harm, found that Primodos caused avoidable harm; further notes that the Government has refused to acknowledge the recommendations by the Independent Medicines and Medical Devices Safety Review relating to Primodos families; and calls on the Government to fully implement the recommendations in the Independent Medicines and Medica al Devices Safety Review and to set up a redress fund for families affected by Primodos.

I thank the Backbench Business Committee for granting this debate. This is now the fifth time we have had a debate trying to persuade the Government to grant justice to families affected by Primodos. I cannot even begin to count the number of times in the last 12 years that this issue has been raised on the Floor of this House during Prime Minister’s questions, Health questions, business questions and even Treasury questions. Time and again, this Government have insisted that there is no credible evidence to support an association between Primodos and deformities. Indeed, they have gone to great lengths to try to prove that there is no association at all.

I remind this House that Primodos was a tablet given to patients by their general practitioner as a pregnancy test. It was 40 times—I repeat, 40 times—the strength of an oral contraceptive today. It does not take a scientist to imagine what a dosage of that strength would do to a foetus. Babies were born with severe deformities, babies who are now adults in their 40s and 50s and have lived their whole lives with these disabilities.

[Sir Mike Penning (Hemel Hempstead) (Con)]

May I take the hon. Lady back a few moments to the tablets that were given by the patient’s GP in a national health surgery, paid for by the national health, and the doctor was paid by the national health? It was not private clinics, but the national health giving this drug.

[Yasmin Qureshi]

I thank the right hon. Gentleman for his intervention. It is important to stress that it was the state, the NHS, involved in this.

In July 2015, I stood in this House and urged the Government to disclose all the evidence they had and to set up an independent inquiry. The then Minister, the hon. Member for Mid Norfolk (George Freeman), heard those concerns and agreed to an independent review, which would be led by an expert working group.

However, first, the expert working group was not independent. In fact, many of the experts were found to have conflicts of interest with the industry. Secondly, the review of the evidence conveniently ignored several important studies and then later said, “Oh, well, there was insufficient evidence.” Thirdly, the terms of reference of the review had said that it would try to find a possible link. Yet the reports’ conclusion said it was unable to find a “causal link”. How exactly does the Government intend to find a causal link, short of testing the drug on pregnant women?

Welfare Reform (Sick and Disabled People)

Debate between Yasmin Qureshi and Mike Penning

Thursday 27th February 2014 Commons Chamber

[Mike Penning]

Actually, I was going to refer to the work by Dr Duffy, and when we leave the Chamber today, I will ask my officials to contact Dr Duffy and his team to see whether we can work closely together. Perhaps we can give them better information so we can be as accurate as possible.

The right hon. Member for Stirling (Mrs McGuire) said my heart is in the right place, and I hope it is. I consider it a great honour to do this job and I desperately want to make things right and proper. If we look at the spending since 2009 going forward and projected into 2015, we see that the budget in this area of Government expenditure will continue to rise. We have a slightly more cumulative figure than the ones I cited earlier, and it is about £50 billion a year, so we spend just under £1 billion a week in this budget. The key for everybody in the House is how we spend it—that we spend it correctly.

I also believe in having a work capability assessment. I do not agree with the motion, but I do agree with the shadow Minister. I think that the assessment was brought in for the right reasons. I am not going to say all the problems were caused by the previous Administration because, frankly, the problems with Atos and the WCA have been there for everybody to see since the general election as well. It is not quite as simple as saying, as some Members have, that we should go out tomorrow morning and sack Atos. It has a contract. As I said at oral questions earlier in the week, I am determined that once we have negotiated the position with Atos—and we are in negotiation with Atos, which is why I was so surprised to read the views of Atos in the press over the weekend—we must make absolutely sure taxpayers’ money is not paid to Atos as compensation for the end of the contract when that comes. That would be fundamentally wrong and I would not agree to it. The negotiations continue.

We have discussed several aspects of benefits today, and I believe that the time being taken for people to be assessed is fundamentally unacceptable. This is an issue not only for the suppliers of PIP and the WCA—we have talked about Capita and Atos—but for my Department as well.

[Yasmin Qureshi]

rose—

[Mike Penning]

I want to make some progress, but I promise that I will give way to the hon. Lady in a moment.

--- Later in debate ---

[Mike Penning]

If we were to inform claimants and Members of Parliament about the minutiae of every single change in policy, we would be here a lot longer. As most Members know, I am not hugely party political, but I must point out that the previous Administration did not offer that level of information either. That is not how Governments work. We are trying to deal with the delays, and to ensure that people get what they are entitled to as quickly as possible and that nobody will be worse off while we are doing that. We are, however, in the middle of a really difficult negotiation with Atos over the WCA.

I want to talk about how we can speed things up. Yesterday, I chaired a meeting of a network involving all the major stakeholders and charities. I hope that I will not upset any of the charities by leaving them out. It was a positive meeting, at which I said to them, “Sit with us and work with us to help us improve on what we have.” I was very much in listening mode, which is why I shall now give way to the hon. Member for Bolton South East (Yasmin Qureshi).

[Yasmin Qureshi]

I am not going to make a party political point; my comment is meant to assist the Minister. On a voluntary basis, I have represented people appealing against assessments now, under the current system, as well as 20-odd years ago under the old system. The problem now lies with the assessment method, which involves only form-filling and box-ticking. That is why we can no longer assess people’s disabilities properly. In the old days, a medical expert gave evidence on a person’s ability. If we were to bring doctors back into the equation, we might find that more decisions were made properly.

[Mike Penning]

I am almost sorry that I gave way to the hon. Lady, because her intervention was so long. My time is being massively eroded, and I hope, Madam Deputy Speaker, that you will give me a few more minutes to address the issues that have been raised.

The consultants and GPs tell us that the clinical evidence taken at the assessment is vital. When they carry out an assessment, they are not there to provide a diagnosis; they are there to assess capacity. They can do that only by using an evidence base. One of the big issues under DLA was that only 6% of applicants ever got a face-to-face assessment. We are at 97% now with PIP. I agree that that is fundamentally too high, as I said to the Select Committee.

I have also attended tribunals to see what is happening during the last part of the DLA claims that are now coming through. I listened to the cases, and I agreed that some of them should never have come before the tribunal in the first place. Under PIP, we have mandatory reconsideration; that was never the case before. I have now asked my officials to go through the approximately 30,000 cases waiting to go to tribunal. We will mandatorily assess all of them, to try to prevent so many from going to tribunal. There is a lot of work to be done, but we must do as much as we can, together with the charities and the representative bodies.

Residential colleges were mentioned earlier. I agree that they do excellent work, but the college principals know that I cannot pay for places that are not taken up. That is what was happening under the previous contract. There were residential places with nobody in residence, and we had day people on day courses. We have worked with the colleges on that, and we will ensure that we have the necessary capacity. Interventions have eroded my time, so I shall now listen to what the hon. Member for Hayes and Harlington (John McDonnell) has to say; I think I know what it will be. Please, let us work together to ensure that the system is better for everyone we represent.