Health Systems in Transition - Hungary - World Health Organization ...
Health Systems in Transition - Hungary - World Health Organization ...
Health Systems in Transition - Hungary - World Health Organization ...
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<strong>Health</strong> systems <strong>in</strong> transition <strong>Hungary</strong> 151<br />
the use of pharmaceutical treatment for a given patient (2005/4). Only one<br />
pharmaceutical is allowed per prescription (2004/5). The prescription must<br />
<strong>in</strong>clude <strong>in</strong>formation about the patient and the prescriber, the name of the<br />
pharmaceutical or its active <strong>in</strong>gredient, its quantity and its dosage (<strong>in</strong>dicated<br />
daily dose) (2004/5). The prescribed quantity may not exceed the quantity<br />
necessary for one month’s treatment, with the exception of patients with chronic<br />
conditions to whom pharmaceuticals can be prescribed for up to three months<br />
or, <strong>in</strong> exceptional cases, up to one year (2004/5).<br />
There are two major types of reimbursement: <strong>in</strong>dication-related and fixed. In<br />
the first category, the <strong>in</strong>dication for a certa<strong>in</strong> substance needs to be confirmed<br />
by a specialist. Some pharmaceuticals for less severe chronic conditions are<br />
covered up to 90%, 70% or 50% of the agreed retail price, while medications<br />
for the more severe, life-threaten<strong>in</strong>g diseases are covered 100% (however,<br />
<strong>in</strong> most cases a m<strong>in</strong>imum patient co-payment, the so-called package fee, of<br />
approximately €1 must still be paid). In the second category, all <strong>in</strong>dications<br />
determ<strong>in</strong>ed <strong>in</strong> the licence of a medication are covered, either up to a fixed<br />
amount (through the reference pric<strong>in</strong>g system) or on a percentage basis (80%,<br />
55% or 25% of the agreed price). The reference pric<strong>in</strong>g system is used for<br />
products with identical active <strong>in</strong>gredients or similar therapeutic effects. In the<br />
case of products with identical active <strong>in</strong>gredients, the basis for reimbursement is<br />
the daily treatment cost of the reference product, which is the product available<br />
on the market for at least six months with the lowest daily treatment cost and<br />
with a market share exceed<strong>in</strong>g 1% (as expressed <strong>in</strong> days of treatment). All<br />
pharmaceuticals conta<strong>in</strong><strong>in</strong>g the same active <strong>in</strong>gredient receive the same subsidy<br />
per daily dose. The reference pric<strong>in</strong>g system also applies to products with<br />
different active <strong>in</strong>gredients but similar therapeutic effects (2004/4). Further<br />
<strong>in</strong>formation on reimbursement can be found <strong>in</strong> section 2.8.4.<br />
There is a system of exemptions from user charges for pharmaceuticals,<br />
medical aids and prostheses, and rehabilitation services for social service<br />
beneficiaries (1993/1). When this system was <strong>in</strong>troduced, eligible <strong>in</strong>dividuals<br />
received all pharmaceuticals on a special list free of charge, with no consumption<br />
or spend<strong>in</strong>g limits. In 2006 the government <strong>in</strong>troduced new rules to tackle<br />
abuse of the system. Eligible <strong>in</strong>dividuals are now granted a monthly personal<br />
budget of up to HUF 12 000 (about €45) to cover user charges on recurrent<br />
health expenditure associated with chronic diseases; these <strong>in</strong>dividuals also<br />
have an addition budget of HUF 6000 (about €24) for acute problems (2005/8).<br />
The range of accessible medic<strong>in</strong>es is no longer restricted, but any spend<strong>in</strong>g<br />
above the budget ceil<strong>in</strong>g must be paid out-of-pocket. Entitlement to user charge