The Medical Cannabis Access Programme is not yet operational.
In the meantime it is open to a medical practitioner wishing to prescribe cannabis for medical purposes for an individual patient under their care to apply to the Minister for Health for a licence, under Section 14 of The Misuse of Drugs Acts 1977 to 2016 and the Regulations made thereunder.
It should be noted that it is the decision of the clinician, in consultation with their patient, to prescribe or not prescribe a particular treatment for a patient under their care. As Minister for Health I have no role in the clinical decision making process.
In line with the Chief Medical Officer's advice, the granting of a licence for cannabis for medical purposes must be premised on an appropriate application being submitted to the Department of Health, which is endorsed by a consultant who is responsible for the management of the patient and who is prepared to monitor the effects of the treatment over time.
To date licences have been issued in respect of twenty individual patients under this provision of the Act.
The Medical Cannabis Access Programme
The Health Products Regulatory Authority’s (HPRA) report ‘Cannabis for Medical Use – A Scientific Review’ recommended that if access to cannabis is to be permitted for medical purposes, its use should only be initiated as part of a structured process of formal ongoing clinical evaluation, in a limited number of clearly defined 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.
All such patients should be under the direct supervision of an appropriately trained and experienced medical consultant. The specified medical conditions (medical indications) are:
- Spasticity associated with multiple sclerosis;
- Intractable nausea and vomiting associated with chemotherapy;
- Severe, refractory (treatment-resistant) epilepsy.
The purpose of the Medical Cannabis Access Programme is to facilitate access to cannabis-based products or preparations that are of a standardised quality and which meet an acceptable level of quality assurance during the manufacturing process.
The Medical Cannabis Access Programme has not yet been established but good progress is being made:
1. clinical guidelines have been drawn up and published,
2. secondary legislation is being drafted to underpin the Programme,
3. cannabis products for use under the Programme, once reviewed as suitable for medical use, will be published on an ‘approved list’.
Department officials are working intensively on finding solutions to the supply of appropriate products for Irish patients.
Department of Health Website
The Department of Health website contains detailed information on medical cannabis, including clinical guidance on the use of medical cannabis. It is updated in the event of new developments on the issue.