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Written Question
Coronavirus: Vaccination
Thursday 24th October 2024

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government whether the medical assessors for the Vaccine Damages Payment Scheme have access to the scientific advice given to ministers regarding the AstraZeneca Covid-19 Vaccine.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

All claims to the Vaccine Damage Payment Scheme (VDPS) are assessed on a case-by-case basis by experienced independent medical assessors, General Medical Council registered doctors with a licence to practise, who have undertaken specialised training in vaccine damage and disability assessment.

When making medical assessment through the VDPS, independent medical assessors consider not just the claimant’s full medical records once they are gathered, but also the claim form and a range of credible resources to support their assessment, as per NHS Business Services Authority’s published VDPS Principles of Medical Assessment. This includes, but is not limited to, the Medicines and Healthcare products Regulatory Agency’s data, including Yellow Card information on suspected safety concerns involving a healthcare product, vaccine product information and updates, the UK Health Security Agency's Green Book, and the World Health Organization’s Causality assessment of an adverse event following immunization. Medical assessors will also consider academic research, epidemiological evidence, and the current consensus of expert medical opinion.


Written Question
Guillain-Barré Syndrome
Thursday 24th October 2024

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government how many cases of Guillain-Barré syndrome have been recorded in each of the last ten years.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

The information is not held in the format requested. However, the following table shows a count of the Finished Admission Episodes (FAEs) where the primary diagnosis was Guillain-Barré syndrome, for the period 2014/15 to 2023/24 in England:

Year

FAEs

2014/15

1,403

2015/16

1,354

2016/17

1,412

2017/18

1,342

2018/19

1,337

2019/20

1,354

2020/21

921

2021/22

1,243

2022/23

1,374

2023/24

1,367

Source: data is from the Hospital Episode Statistics, by NHS England.
Notes:

  1. admissions do not represent the number of patients, as a person may have more than one admission within the period;
  2. an FAE is the first period of admitted patient care under one consultant within one healthcare provider, and are counted against the year or month in which the admission episode finishes; and
  3. this data refers to activity in English National Health Service Hospitals and English NHS commissioned activity in the independent sector.


Written Question
Coronavirus: Vaccination
Thursday 24th October 2024

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government whether they will publish the scientific advice they received from the Joint Committee on Vaccination and Immunisation between 1 April and 6 May 2021 regarding age restrictions for the AstraZeneca COVID-19 Vaccine.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

The Joint Committee on Vaccination and Immunisation (JCVI) provided advice to the Government between 1 April and 6 May 2021 regarding age restrictions for the AstraZeneca COVID-19 vaccine. This advice was published on the GOV.UK website, and states that the JCVI currently advises that it is preferable for adults aged less than 30 years old, without underlying health conditions that put them at higher risk of severe COVID-19 disease, to be offered an alternative COVID-19 vaccine, if available.

Discussions on the AstraZeneca vaccine also took place and are noted within the minutes of the JCVI’s COVID-19 sub-committee meetings held on 13, 22, and 29 April 2021. The outcome of the discussions held within these meetings was reflected in the updated JCVI advice on the use of the AstraZeneca vaccine, published on the 7 May 2021, which extended the preferential use of alternative vaccines to unvaccinated adults aged 30 to 39 years old, who are not in a clinical priority group at higher risk of severe COVID-19 disease.


Written Question
Coronavirus: Vaccination
Thursday 24th October 2024

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government how many applicants to the Vaccine Damages Payment Scheme (VDPS) have made a claim relating to the AstraZeneca Covid-19 Vaccine; and how many applicants to the VDPS have been waiting for a decision for longer than (1) one year and (2) 18 months.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

As of 30 September 2024, the Vaccine Damage Payment Scheme (VDPS) has processed 3,825 claims relating to the AstraZeneca COVID-19 vaccine. A further 207 claims relating to the AstraZeneca COVID-19 vaccine are undergoing medical assessment. As of 30 September 2024, there were 7,335 live VDPS claims, of which 1,024 have been awaiting resolution for longer than 12 months, and 316 claims for longer than 18 months.


Written Question
Coronavirus: Vaccination
Tuesday 22nd October 2024

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government when they received scientific advice detailing an increase in the incidence of autoimmune illness and a possible link between that increase and the AstraZeneca COVID-19 Vaccine.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

Following reports of extremely rare adverse events of concurrent thrombosis and thrombocytopenia following vaccination with the first dose of the AstraZeneca COVID-19 vaccine, the Joint Committee on Vaccination and Immunisation (JCVI) advised that adults aged under 30 years old and without underlying health conditions should be offered an alternative vaccine, if available. This advice was published on 7 April 2021. In parallel, the Medicines and Healthcare products Regulatory Agency updated its information for healthcare professionals on the COVID-19 AstraZeneca vaccine. On 7 May 2021, the JCVI published updated advice which extended the group who should be offered an alternative to include all unvaccinated adults aged 30 to 39 years old who were not in a clinical priority group at higher risk of severe COVID-19 disease. This advice is published online, and is available in an online only format.


Written Question
Coronavirus: Vaccination
Tuesday 22nd October 2024

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government what scientific advice they received between 1 April and 6 May 2021 regarding age restrictions for the AstraZeneca COVID-19 Vaccine.

Answered by Baroness Merron - Parliamentary Under-Secretary (Department of Health and Social Care)

Following reports of extremely rare adverse events of concurrent thrombosis and thrombocytopenia following vaccination with the first dose of the AstraZeneca COVID-19 vaccine, the Joint Committee on Vaccination and Immunisation (JCVI) advised that adults aged under 30 years old and without underlying health conditions should be offered an alternative vaccine, if available. This advice was published on 7 April 2021. In parallel, the Medicines and Healthcare products Regulatory Agency updated its information for healthcare professionals on the COVID-19 AstraZeneca vaccine. On 7 May 2021, the JCVI published updated advice which extended the group who should be offered an alternative to include all unvaccinated adults aged 30 to 39 years old who were not in a clinical priority group at higher risk of severe COVID-19 disease. This advice is published online, and is available in an online only format.


Written Question
Folic Acid: Prescriptions
Tuesday 12th December 2023

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government whether they will request NHS England to permit the prescription of Thiamine capsules as an alternative to tablets.

Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)

Clinicians are responsible for making prescribing decisions for their patients, considering best prescribing practice and appropriate national and local guidance.

In respect of the prescribing of unlicensed medicines, the National Health Service’s long-established practice is reflected in professional guidance. Individual patient needs should be fulfilled by, firstly, using a licensed medicine within its licensed indication, or if there is nothing suitable, using a licensed medicine outside its licensed indication. If there is still nothing suitable after this, the clinician can consider using an unlicensed medicine.

Thiamine tablets are available as a licensed medicine. Thiamine capsules are not a licensed medicine. Thiamine supplements can be purchased from pharmacies or shops. These include vitamin B complex tablets and multivitamin tablets where thiamine is listed as an ingredient. NHS guidance states that vitamins and minerals should not be routinely prescribed in primary care as there is insufficient high-quality evidence to demonstrate their clinical effectiveness. However, subject to funding, a clinician can prescribe any product on the NHS that they consider to be clinically necessary for the treatment of their patient unless it is listed in Schedules 1 or 2 of the NHS (General Medical Services Contracts) (Prescription of Drugs etc.) Regulations 2004. Parts XVIIIA and XVIIIB of the NHS Drug Tariff list the drugs, medicines and other substance that may not be ordered, or may only be ordered on the NHS in certain circumstances under the above regulations.


Written Question
Embryos: Research
Wednesday 26th July 2023

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government what steps they are taking to ensure the "special status” of the human embryo continues to be upheld in any decisions related to human embryo research; and whether they will make an assessment of the recent Human Fertilisation and Embryology Authority consultation, in particular given that it omitted any mention of the protected “special status” of the embryo or any related ethical considerations.

Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)

The Human Fertilisation and Embryology Authority (HFEA) has advised that any decisions related to human embryo research are undertaken in accordance with the Human Fertilisation and Embryology Act 1990 (as amended). The Government asked the HFEA to undertake a stakeholder dialogue to identify priorities for modernisation of the Act in 2021, and the report of this work is not expected to be completed until autumn 2023.


Written Question
Abortion: Drugs
Friday 21st July 2023

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government whether they intend to review the safety of abortion pills being sent by post.

Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)

The Government has no current plans to commission a review into the practice of sending pills for women to carry out early medical abortion at home.


Written Question
Abortion: Prosecutions
Thursday 13th July 2023

Asked by: Lord Moylan (Conservative - Life peer)

Question to the Department of Health and Social Care:

To ask His Majesty's Government what assessment they have made of the prosecution of Carla Foster for an offence under section 58 of the Offences Against the Person Act 1861; and what consideration they have given to proposing legislation to prevent similar cases from happening, in particular, by reintroducing the requirement for women to be seen in-person at least once before being issued abortion pills.

Answered by Lord Markham - Shadow Minister (Science, Innovation and Technology)

No assessment has been made. Decisions to prosecute in England and Wales are a matter for the independent Crown Prosecution Service (CPS). As with all criminal offences, in deciding whether to bring a prosecution the CPS will apply the two-stage test in the Code for Crown Prosecutors: whether there is sufficient evidence to provide a realistic prospect of conviction; and whether a prosecution is needed in the public interest.

Parliament voted to amend the Abortion Act 1967 to allow women in England and Wales to take one or both pills for early medical abortion at home. Women should be given the choice to either have an in-person consultation with a clinician or to have a virtual consultation, and if eligible, will be able to take both pills for early medical abortion at home. We have been clear that abortion providers should not move to a digital by default approach.

There are no plans to review or change abortion laws. As with other matters of conscience, abortion is an issue on which the government adopts a neutral stance.