Discussions of European medicines policy must take into account
a number of conflicting factors (public health, individual patients,
economic and financial interests, etc.
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For those seeking in-depth information, some texts published in
la revue Prescrire have never been more topical.
Charter of fundamental rights of the European
Union
Several articles of the Charter of fundamental rights of the European
Union provide for specific rights to health and social protection.
Other articles described citizens' means and rights with regard
to the European institutions: rights to be defended and implemented.
To download (79 Ko, PDF format): Click
here
What defines real therapeutic advance?
La revue Prescrire issue 225, pp. 81 and 140-145
Full text of the declaration by ISDB (International Society of Drug
Bulletins), Paris 15-16 November 2001. Don't mistake the terms "new
product" or "innovation" for real therapeutic advance;
keep patients' interests uppermost.
To download (160 Ko, PDF format): Click
here
Biomedical research: patients' interests first
La revue Prescrire issue 219, pp. 539-540 and 542-543
Full text of the Helsinki Declaration by the World Medical Association,
October 2000. New treatments must be evaluated relative to the best
existing options; placebos must only be used if no drugs with proven
efficacy are available.
To download (26 Ko, PDF format): Click
here
Towards transparency of official decisions on medicines
La revue Prescrire issue 172, pp. 229 and 277-281
Full text of the Uppsala Declaration coordinated by Health Action
International Europe and the Swedish foundation Dag Hammarskjöld,
Uppsala 11-14 September 1996. The basic principles, obstacles and
means for promoting transparency and accountability in drug regulation.
To download (29 Ko, PDF format): Click
here
Access to drug safety information
La revue Prescrire issue 187, p. 599
Full text of the Erice Declaration adopted following the international
conference on pharmacovigilance communication organised, among others,
by the Uppsala WHO collaborating centre for drug safety, Erice 24-27
September 1997, under the aegis of the World Health Organisation.
Institutional duty to offer information and transparency on medicines.
To download (23 Ko, PDF format): Click
here
Internet: medicines agencies have a duty to inform
La revue Prescrire issue 218, p. 464
Prescrire's rating system for agency websites. La revue Prescrire
has used this system to compare the FDA website (La revue Prescrire
issue 221, p. 705-706) and the EMEA website (La revue Prescrire
issue 228, p. 386-388).
To download (146 Ko, PDF format): Click
here
Also published in la revue Prescrire:
Think INN, prescribe INN: good professional
practice
La revue Prescrire issue 209, pp. 561 and 606-623
An authoritative review (see also "Les médicaments génériques",
a detailed file: 232 pages, last update February 2002). Drug management
based on international non proprietary names (INN), including prescription
and dispensing, is a key determinant of quality of care.
For further information (in French): Click here
Pricing of reimbursed drugs: what rationale?
Part I - the 1990s: worldwide deregulation hinders drug price control
La revue Prescrire issue 222, pp. 782-786
Part II - Price proportional to the degree of innovation: a good
principle but poor impact
La revue Prescrire issue 223, pp. 801 and 859-863
Free trade within the European Union hinders drug price control.
Drug companies have too much leeway.
©La revue Prescrire 1 October 2003
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