Budgetary Impact of Covering “Me-Too” Drugs from Social Security: Buenos Aires State Case Report
Abstract
The majority of new drugs that are register at Health Global Market are not considered real innovations and due to their chemical structure similarity of reference’s group drug, they are known as “me-too”. These “me too” drugs has no additional therapeutic benefits but greatly increasing treatment´s. PURPOSE: To demonstrate the economic impact in Social Security budget by covering “me too” medicines. METHODS: An epidemiological-descriptive-analytical study was performed in order to analyze the burden of anti-hypertensive prescription from patients under coverage by Buenos Aires State Social Security. Two types of medicines were compared: “pioneer” or “me-too”. Variables considered were: type of drug, class or therapeutical group of medicines, global costs, burden for social security and for patients. RESULTS: From 185865 patients that received medication; in 121748 of the cases the strategy was monotherapy while 64117 received at least two or more medicines. 189714 were reference drugs while 64393 of them were considered “me-too”. In average, “me-too” drugs were 41.23% more expensive than classical treatment. The percentage covered by IOMA varies according to the medicines (between 45 to 51%) and patients must complete the amount of money remaining from their pockets. Paradoxically, the percentage covered by IOMA some “me-too” were greater than the percentage paid for most classic medications of each group. CONCLUSIONS: By only choosing the drug of reference, with proven effectiveness, from each therapeutical group, the State Social Security could cover 100% of the cost of all anti-hypertensive treatment and all patients even saving almost 2 million dollars per year.
Keywords: Health, Policies, Medicines, Me too, Economical Burden, Coverage, anti-hypertensive
Keywords:
Health, Policies, Medicines, Me too, Economical Burden, Coverage, anti-hypertensiveDOI
https://doi.org/10.22270/jddt.v10i3-s.4087References
Marin GH, Polach A. High-cost drugs: analysis and proposals for the Mercosur countries. Rev Panam Salud Publica, 2011; 30(2):167–76
Jena AB, Calfee JE, Mansley EC, Philipson TJ. 'Me-Too' Innovation in Pharmaceutical Markets. Forum Health Econ Policy, 2009; 12(15-10.
Correa CM. “Me-too medicines are new chemical entities developed for pharmaceutical use that do not include any genuine therapeutic improvement”. In: Correa C. “Ownership of knowledge: the role of patents in pharmaceutical R&D.” Bull World Health Organ 2004; 82(10):785-6.
DiMasi JA. Price Trends for Prescription Pharmaceuticals: 1995–1999. Background report prepared for the U.S. Department of Health and Human Services’ Conference on Pharmaceutical Pricing Practices, Utilization and Costs USG, Washington, D.C., USA, 2000.
Garattini S. Are me-too drugs justified? J Nephrol, 1997; 10(6):283-94.
diMasi J & C Paquette. “The Economics of Follow-on Drug Research and Development Trends in Entry Rates and the Timing of Development.” Pharmacoeconomics, 2004; 22(2):1-14.
Kessler DA, Rose JL, Temple RJ, Schapiro R, Griffin JP. Therapeutic-Class Wars–Drug Promotion in a Competitive Marketplace. New Engl. J Med, 1994; 331(20):1350–3..
Calfee, J.E. Prices, Markets, and the Pharmaceutical Revolution. Washington DC: American Enterprise Institute Press, AEP, Washington, DC, USA, 2000.
Hogerzeil HV. Promoting Rational Prescribing: An International Perspective. British Journal of Clinical Pharmacology, 1995; 39:1–6.
Hogerzeil HV, et al. Field Tests for Rational Drug Use in Twelve Developing Countries. Lancet, 1993; 342:1408–1410.
Lee TH. “Me-Too” Products–Friend or Foe? New New Engl. J Med, 2004; 350(3):211–2.
Lichtenberg FR, Philipson TJ. The Dual Effects of Intellectual Property Regulations: Within- and between-Patent Competition in the U.S. Pharmaceuticals Industry. Journal of Law and Economics, 2002; 45:643–672.
Régnier S. What is the value of 'me-too' drugs? Health Care Manag Sci, 2013; 16(4):300-313.
Marín GH, Canas M, Homar C, Perrotta M Drug utilization from Program REMEDIAR in Buenos Aires, Argentina. Latin America Journal of Pharmacy, 2008; 27:535-542.
Marin GH., Risso P., Sbatella D., Haag G.Treatment adherence by personalizing the drug dispensing for diabetic patients in social vulnerable situation .Quality in Primary Care, 2015; 23(2):93-96.
Published


How to Cite
Issue
Section
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgment of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).