Citizens of the European Union have become more empowered and proactive consumers of healthcare, increasingly seeking information about medicines and treatments. EU citizens want to be able to access information on existing medicines and treatments and at the same time to be more actively involved in making decisions regarding their health, says the European Commission. With the increased Internet use, ensuring the reliability and quality of information, particularly on websites, has become fundamental. Action at EU level is aimed at benefiting EU citizens in many ways. First and foremost, the information provision will be improved and harmonized across the EU. There will be more possibilities to receive high quality objective and non-promotional information. Secondly, European citizens will be able to receive information that is in line with EU legislation. This reduces the risk of receiving misleading and bad quality information.
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EU citizens have across the EU. Although advertising of prescription-only medicines to the general public is forbidden, a lack of detail on information provision has led to a situation in which Member States interpret EU legislation in very different ways and have developed divergent practices on the provision of information on medicinal products. Harmonization at EU level can contribute to changing the current situation and promoting public health across the EU. This is of major importance in particular in the era of the Internet where citizens can access information from all over the world.
There are a on medicinal products, most notably through consultations with healthcare professionals. However, bearing in mind that patients have become more independent and empowered as regards their own health, they also actively seek information by themselves. Consequently, other sources of information are needed.
The European Commission has prepared a legal proposal on information to patients. Specifically, it proposes
- that companies can make information on their prescription-only medicines available to the general public,
- while maintaining the existing advertisement ban
The of the legal proposal are:
about prescription-only medicines is allowed:
- , labelling and package leaflets, as approved by the competent authorities;
- information which does , labelling and patient information leaflet of the medicinal product, but presents them in a different way;
- information on the of the medicine, prices and factual, informative announcements and reference material relating, for example, to pack changes or adverse-reaction warnings;
- about non-interventional scientific studies, or accompanying measures to prevention and medical treatment or information which presents the medicinal product in the context of the condition to be prevented or treated shall be allowed.
Only for the dissemination of information shall be allowed:
- health-related publications as defined by the Member State of publication, to the exclusion of unsolicited material actively distributed to the general public;)
- on medicinal products, to the exclusion of unsolicited material actively distributed to the general public;
- to request for information of a member of the general public.
All the information provided shall fulfil :
- ; in this regard, if the information refers to the benefits of a medicinal product, its risks shall also be stated;
- take into account the ;
- and be verifiable and include a statement on the level of evidence;
- and include the date of publication or last revision of the information;
- , factually correct and not misleading;
- for the general public or members thereof;
- clearly indicating the author and giving references to any documentation that the information is based on;
- , labelling and patient information leaflet of the product, as approved by the competent authorities.
The information made available will be monitored by Member States. In general, the information shall be subject to control of information prior to its dissemination. Internet sites containing information on prescription-only medicinal products shall be registered and monitored by the Member States.
The proposal will now be transmitted to the European Parliament and the Council where it will be discussed and voted in the co-decision procedure. The legal proposal could become law at the earliest in 18 months following adoption and publication by the European Parliament and the Council.
More information on information to patients on prescription-only medicinal products
