Written answers

Wednesday, 10 July 2024

Department of Health

Cannabis for Medicinal Use

Photo of David CullinaneDavid Cullinane (Waterford, Sinn Fein)
Link to this: Individually | In context | Oireachtas source

408. To ask the Minister for Health for an update on the medical cannabis access programme; the number of approved products under the scheme; the number of actively supplied products under the scheme which are available in the state; the number of individuals availing of the scheme; and the number of individuals approved for the scheme who cannot access a product on the scheme. [30418/24]

Photo of David CullinaneDavid Cullinane (Waterford, Sinn Fein)
Link to this: Individually | In context | Oireachtas source

409. To ask the Minister for Health if he is considering any products or conditions for addition to the medical cannabis access programme. [30419/24]

Photo of Stephen DonnellyStephen Donnelly (Wicklow, Fianna Fail)
Link to this: Individually | In context | Oireachtas source

I propose to take Questions Nos. 408 and 409 together.

There are 10 products meeting the definition of "specified controlled drug" in S.I. 262/2019, the Misuse Of Drugs (Prescription And Control Of Supply Of Cannabis For Medical Use) Regulations 2019, however 2 products, made by Aurora, have not been brought to market by the manufacturer.

There are 55 approved individuals on the MCAP register since its implementation in November 2021. The HSE, operationally responsible for the MCAP, is not aware of any patients who cannot access the products under MCAP.

Prospective suppliers of products to the Medical Cannabis Access Programme can apply to the Health Products Regulatory Authority (HPRA), acting on behalf of the Minister for Health, to have a cannabis product considered for inclusion in the schedule to the Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) Regulations 2019. Applicants must provide evidence to demonstrate that the proposed cannabis product meets the requirements of a ‘specified controlled drug’ as defined in the MCAP legislation. The onus is on prospective suppliers to submit applications to the HPRA. The HPRA is currently considering 3 applications for products to be added to the MCAP.

My Department is in the process of establishing a Clinical Review Group. While I cannot put a definitive timeline on the work of the clinical review group, it is my ambition that the review will be completed by the end of this year.

Upon completing its work, the clinical review group will make recommendations to me as Minister for Health as to whether there is sufficient evidence to include other conditions in the Medical Cannabis Access Programme.

Photo of David CullinaneDavid Cullinane (Waterford, Sinn Fein)
Link to this: Individually | In context | Oireachtas source

410. To ask the Minister for Health the number of Ministerial licenses currently in use for medical cannabis. [30420/24]

Photo of Stephen DonnellyStephen Donnelly (Wicklow, Fianna Fail)
Link to this: Individually | In context | Oireachtas source

A Ministerial Licence issued pursuant to Section 14 of the Misuse of Drugs Act 1977, entitles the clinician licensee to prescribe, import, supply, possess and administer a cannabis-based product containing Tetrahydrocannabinol.

To date 372 Ministerial Licences have been issued to clinicians for the treatment of 77 different patients. Currently 28 patients are being treated under the programme.

Comments

No comments

Log in or join to post a public comment.