WHAT HAPPENS TO ORIGINATOR MEDICINES WHEN (GENERIC) FOLLOWERS ENTER THE PUBLIC MARKET
Author(s)
Habl CA1, Leopold C2
1Austrian Public Health Institute GÖG, Vienna, Austria, 2Harvard Medical School & Harvard Pilgrim Healthcare Institute, Boston, MA, USA
OBJECTIVES: Many pharmaceutical companies claim that because of European national pricing regulations, namely the wide-spread policy of external reference pricing some off-patent originator products disappeared from the public market. We investigated likelihood and timelines for occurrence. METHODS: Panel data from Euripid database were extracted for seven major substances in national public markets. All strengths, presentations and packs were considered. We defined public market as fully or partly publicly funded reimbursable medicines. Euripid features information on reimbursable medicines (including prices) from 28 European countries. We checked if originators were marketed at different time periods between 2010 and May 2016 and if relevant – when they had been delisted. RESULTS: In 2016 the originator brand was not reimbursed
- Atorvastatin in Poland and Estonia,
- Clopidogrel in five countries
- Donezepil in eight countries,
- Omeprazole in 13 countries,
- Olanzapine in Estonia, Latvia, Poland and Slovakia,
- Paroxetine in six countries,
- Valproic acid in Bulgaria, Iceland and Estonia.
Conference/Value in Health Info
2016-10, ISPOR Europe 2016, Vienna, Austria
Value in Health, Vol. 19, No. 7 (November 2016)
Code
PHP26
Topic
Health Policy & Regulatory
Topic Subcategory
Pricing Policy & Schemes
Disease
Multiple Diseases
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