Literature DB >> 10160088

Switching the histamine H2 receptor antagonist famotidine to nonprescription status in Canada. An economic evaluation.

R F Tasch1, R Goeree, C J Henke, B J O'Brien.   

Abstract

The aim of this study was to compare the direct medical costs associated with the treatment of patients with heartburn/nonulcer dyspepsia under 2 scenarios: (i) no nonprescription histamine H2 receptor antagonist (H2RA) is available (the 'status quo scenario'); and (ii) the H2RA famotidine (at a daily dosage of 10mg) is available over-the-counter (OTC) at retail pharmacies (the 'OTC scenario'). We employed a decision analysis model over a 16-week period that considered direct medical costs from 2 alternative perspectives: (i) society, including the cost of self-medication borne by patients; and (ii) a provincial third-party payer for healthcare. Data concerning direct medical costs associated with consumer self-medication and physician prescription of medication (including pharmacist dispensing fees), tests and procedures, and consultations with general practitioners and specialists were drawn from a clinician panel, published unit costs, and special surveys of institutional databases. All costs are reported in 1993 Canadian dollars ($Can; $Can1 = $US0.72, October 1995). From a societal perspective, the expected cost per patient over a 16-week period is not substantially different between the status quo and the OTC scenarios ($Can98 and $Can96, respectively). From a provincial third-party payer perspective, the expected costs per patient for the same scenarios are $Can95 and $Can89, a saving of $Can6 per patient. These results are sensitive to the proportion of patients who initially choose to see their physician rather than self-medicate, and the percentage of patients achieving successful treatment of symptoms. Changes in the rate or the cost of nonprescription medication, tests/procedures and physician visits do not affect the relative cost rankings. The total number of physician visits remained constant in both scenarios. From the societal cost perspective, the availability of famotidine in nonprescription form yields total costs that are similar to the status quo. However, from the perspective of the provincial payer, the expected costs per patient are likely to be slightly lower than the status quo if famotidine is available in unrestricted OTC scenario use. To generate significant savings to provincial payers, the number of people choosing immediate physician contact would have to be reduced, although not substantially, in the OTC scenario.

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Year:  1996        PMID: 10160088     DOI: 10.2165/00019053-199609010-00007

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  28 in total

1.  The costs and benefits of switching a drug from prescription-only to over-the-counter status: a review of methodological issues and current evidence.

Authors:  F Andersson; E Hatziandreu
Journal:  Pharmacoeconomics       Date:  1992-11       Impact factor: 4.981

Review 2.  An approach to dyspepsia in the ambulatory care setting: evaluation based on risk stratification.

Authors:  S C Zell; M Budhraja
Journal:  J Gen Intern Med       Date:  1989 Mar-Apr       Impact factor: 5.128

Review 3.  Famotidine in gastroesophageal reflux disease (GERD).

Authors:  I C Wesdorp
Journal:  Hepatogastroenterology       Date:  1992-02

Review 4.  Over-the-counter histamine H2-receptor antagonists. How will they affect the treatment of acid-related diseases?

Authors:  S Holt
Journal:  Drugs       Date:  1994-01       Impact factor: 9.546

Review 5.  Over-the-counter drugs. The issues.

Authors:  H Cranz
Journal:  Drug Saf       Date:  1990       Impact factor: 5.606

6.  Reflections on a month in the life of the Ontario Drug Benefit Plan.

Authors:  W McIsaac; C D Naylor; G M Anderson; B J O'Brien
Journal:  CMAJ       Date:  1994-02-15       Impact factor: 8.262

7.  Cimetidine use and gastric cancer.

Authors:  M C Schumacher; S S Jick; H Jick; A D Feld
Journal:  Epidemiology       Date:  1990-05       Impact factor: 4.822

8.  Self-Directed Treatment of Intermittent Heartburn: A Randomized, Multicenter, Double-Blind, Placebo-Controlled Evaluation of Antacid and Low Doses of an H(2)-Receptor Antagonist (Famotidine).

Authors:  Thomas J. Simon; Roger G. Berlin; Andrea H. Gardner; Laura A. Stauffer; A. Lawrence Gould; Albert J. Getson
Journal:  Am J Ther       Date:  1995-05       Impact factor: 2.688

9.  Ranitidine for non-ulcer dyspepsia. A clinical study of the symptomatic effect of ranitidine and a classification and characterization of the responders to treatment.

Authors:  P G Farup; S Larsen; K Ulshagen; M Osnes
Journal:  Scand J Gastroenterol       Date:  1991-11       Impact factor: 2.423

10.  Efficacy of twice daily doses of 40 or 20 milligrams famotidine or 150 milligrams ranitidine for treatment of patients with moderate to severe erosive esophagitis. Famotidine Erosive Esophagitis Study Group.

Authors:  T J Simon; R G Berlin; R Tipping; L Gilde
Journal:  Scand J Gastroenterol       Date:  1993-05       Impact factor: 2.423

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  2 in total

Review 1.  Benefits and risks of self medication.

Authors:  C M Hughes; J C McElnay; G F Fleming
Journal:  Drug Saf       Date:  2001       Impact factor: 5.606

2.  Usage patterns of over-the-counter phenazopyridine (pyridium).

Authors:  Chih-Wen Shi; Steven M Asch; Eve Fielder; Lillian Gelberg; Robert H Brook; Barbara Leake; Martin F Shapiro; Patrick Dowling; Michael Nichol
Journal:  J Gen Intern Med       Date:  2003-04       Impact factor: 5.128

  2 in total

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