France
France-HiT
France-HiT
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162<br />
Health systems in transition <br />
<strong>France</strong><br />
be maintained. However, to date there has been no decree authorizing this<br />
alternative coverage procedure, and the left-wing government elected in 2012<br />
has not put this measure forward since then.<br />
While this cost-containment strategy may be effective in reducing costs in the<br />
short term, the long-term effect is less clear. The French Accounts Commission<br />
has noted that de-listing drugs in a particular therapeutic class can have effects<br />
on prescription of drugs in other covered classes that may reduce or eliminate<br />
the cost savings. For example, when the class of expectorants was de-listed,<br />
savings of €45 million were anticipated. However, prescriptions were shifted<br />
to cough suppressants and bronchodilators, resulting in additional expenditure<br />
of €40 million for these drugs (Cour des comptes, 2011b) and highlighting the<br />
strong culture in French medical practice of offering prescriptions for every<br />
symptom. This underscores the need to address medical practice through, for<br />
example, changes in initial training and DPC (see section 4.2.3).<br />
Price control<br />
Strict control of tariffs was applied, notably to the price of drugs but also to other<br />
type of service such hospital remuneration, medical devices and professional<br />
tariffs. As a result of tight control of doctors’ tariffs, extra-billing, which is<br />
not covered by SHI, was permitted starting in the 1980s for certain categories<br />
of doctor (see Sector 2 doctors; section 3.7.2). However, extra-billing in some<br />
specialties has significantly increased OOP payments, thereby impairing access<br />
in some areas where extra-billing is the rule (e.g. gynaecologists in Paris). For<br />
this reason, policies to reduce extra-billing were developed starting in 2013.<br />
Drug price control<br />
The CEPS (see section 2.7.2) is authorized to reduce previously negotiated<br />
drug prices under four circumstances: at the time of renewal of the agreement,<br />
particularly if there has been a significant increase in volume following<br />
extensions of indications; when the drug’s patent expires and the first generics<br />
enter the positive list (generally 85% of the price of the brand name drug); when<br />
the evolution of drug expenditure threatens ONDAM targets (see section 3.3.3);<br />
or when studies of the drug once it is on the market reveal differences in efficacy<br />
or side-effects compared with the clinical trial data that were considered at<br />
the time the pricing agreement was made. Drug price reductions, both in the<br />
ambulatory and hospital sectors, constitute a significant source of savings in<br />
the annual health budget, with a target of €960 million in 2014 (Sécurité sociale,<br />
2013c).