Holyrood, made browsable

Motions, questions and answers

Every motion, amendment, parliamentary question and answer the chamber has lodged since 1999, searchable in one place.

129
Current MSPs
415
MSPs ever elected
14
Parties on record
305,439
Motions and questions
84,137
Motions
234,089
Questions
Chamber activity

Motions, questions and answers

Last 30 days
292 motions
956 questions · up to 16 Jun 2026
Most-active MSP
23 motions in the last 30 days
Top topic
in 257 titles
Unanswered questions
568
Items shown
0
Motions
0
Questions
0

Covering Unknown to Unknown. 5,653 amendments linked to their parent motions. 59,985,316 recorded MSP supports. 2,901 divisions on record (1,666 carried, 1,208 defeated).

Most common

What kinds of items appear

Written Question 206,214 Standard Motion 63,175 Portfolio Question 10,776 General Question 9,020 Motion For Debate 5,277 Members' Business Motion 5,213 Bureau Motion 5,029 Amendment 3,793 First Minister's Question 3,585 SPCB Written Question 1,621 Inspired Question 1,589 Topical Question 983
Year by year

How many items per year

Showing 0 of 0 matching items in session S6, 10 Jun 2025 – 10 Jun 2026. Latest 30 days: 1,285.
Reference Item MSP Type Date (desc)
Nothing matches those filters — try a broader search or clear a filter.
← Back to list
Question

To ask the Scottish Government, further to the answer to question S6W-13815 by Humza Yousaf on 24 January 2023, whether Palforzia will be approved as a treatment for peanut allergies through the NHS.

S6W-32433 · Written Question · lodged by Burnett, Alexander

Lodged on
17 Dec 2024
Heard / answered on
24 Dec 2024
To ask the Scottish Government, further to the answer to question S6W-13815 by Humza Yousaf on 24 January 2023, whether Palforzia will be approved as a treatment for peanut allergies through the NHS.

The answer

Aimmune Therapeutics, the manufacturer of Palforzia®, had indicated an intention to make a resubmission to the Scottish Medicines Consortium (SMC), however to date this has not been received. The decision on whether to submit, and the timing of that submission, is entirely for the manufacturer of the medicine to make. If they do resubmit, information on the specific timelines for the reassessment will be available via the search facility available on the home page of the SMC’s website here. There is a fast-track resubmission option, which reduces the normal assessment timeline.In the meantime, Health Boards have procedures in place using the Peer Approved Clinical System “PACS Tier Two” process, for clinicians to request the use of licensed medicines on a ‘case-by-case’ basis for individual patients, when the treating clinician considers that there would be significant clinical benefit for a patient.

Answered by Neil Gray on 24 Dec 2024.