Home > Dáil Éireann debate. Question 1399, 1539, 1540 [Medicinal cannabis] [12455/24, 13310/24, 13311/24].

[Oireachtas] Dáil Éireann debate. Question 1399, 1539, 1540 [Medicinal cannabis] [12455/24, 13310/24, 13311/24]. (20 Mar 2024)

External website: https://www.oireachtas.ie/en/debates/question/2024...


Dáil Éireann debate. Question 1399 – Health services [12455/24]

1399. Deputy Brendan Griffin asked the Minister for Health for clarification on a matter (details supplied); and if he will make a statement on the matter. [12455/24]

Minister for Health: It is open to clinicians to apply to the Minister for Health for a licence issued pursuant to Section 14 of the Misuse of Drugs Act 1977 to treat a patient with Schedule 1 cannabis-based products. In these situations it is inappropriate for the Department to discuss such applications with anybody other than the applicant themselves and cannot discuss the matter with the Deputy

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Dáil Éireann debate. Question 1539 – Departmental data [13310/24].

1539. Deputy Violet-Anne Wynne asked the Minister for Health the number of those receiving treatment under the MCAP since the opening of the scheme to date, by year, in tabular form; and if he will make a statement on the matter. [13310/24]

Minister for Health: Patients accepted for treatment under the programme are issued with a CMUR (Cannabis for Medical Use Register) number. Since the commencement of the programme in 2021 53 CMUR numbers have issued, as set out in the table below.

MCAP Register

Number of patients

2021

04

2022

28

2023

21

2024

00

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Dáil Éireann debate. Question 1540 – Departmental programmes [13311/24].

1540. Deputy Violet-Anne Wynne asked the Minister for Health his views on whether he thinks the Medical Cannabis Access Programme has been a success and whether he has faith in its continuation on a permanent basis; and if he will make a statement on the matter. [13311/24]

Minister for Health: The purpose of this Programme is to facilitate compassionate access to cannabis for medical reasons, where conventional treatment has failed. It follows the clear pathway laid out by the Health Products Regulatory Authority in their expert report “Cannabis for Medical Use – A Scientific Review” which stated that the decision to allow cannabis for medical use was as much a societal and policy decision as a scientific one due to the paucity of robust clinical evidence, the recreational use of the product and the strong public and patient led demand.

The report recommended that cannabis should only be made available for the treatment of patients with specified medical conditions which have failed to respond to all other previous treatments, and where there is at least modest evidence that cannabis may be effective.  Such patients should be under the direct supervision of an appropriately trained and experienced medical consultant. The specified medical conditions (medical indications) are:

1. Spasticity associated with multiple sclerosis resistant to all standard therapies and interventions whilst under expert medical supervision;

2. Intractable nausea and vomiting associated with chemotherapy, despite the use of standard anti-emetic regimes whilst under expert medical supervision;

3. Severe, refractory (treatment-resistant) epilepsy that has failed to respond to standard anticonvulsant medications whilst under expert medical supervision. 

It is the decision of the medical consultant, in consultation with their patient, to prescribe a particular treatment, including a cannabis-based treatment, for a patient under their care.

The Department of Health is currently carrying out a clinical review of the programme to ascertain whether evidence exists to expand the range of conditions covered by the programme.

The cannabis-based products used in the programme do not have marketing authorisations and have not been subjected to the same rigorous process as approved medicined with marketing authorisations. The clinical preference is for the use of approved medicines.

It must be acknowledged that since the initial report recommending the Access Programme marketing authorisations have been approved for cannabis-based products such as Epidiolex, dronabinol and nabilone that can be prescribed in the normal manner together with advances in anti-emetics for the treatment of nausea as a result of chemotherapy, treatment options not available at the time of the original recommendations.

To date, 53 patients have availed of treatment under the MCAP.  

Item Type
Dail Debates
Publication Type
Irish-related
Drug Type
Cannabis, Prescription/Over the counter
Intervention Type
Policy
Date
20 March 2024
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