Literature DB >> 15338846

Impact of safety warnings on drug utilization: marketplace life span of cisapride and troglitazone.

Julie J Wilkinson1, Rex W Force, Paul S Cady.   

Abstract

STUDY
OBJECTIVE: To evaluate the impact of safety alerts on the volume of cisapride and troglitazone usage.
DESIGN: Retrospective database analysis.
SETTING: University research center. MATERIAL: Idaho Medicaid claims data from January 1994--July 2000.
MEASUREMENTS AND MAIN RESULTS: Monthly counts of total and new prescriptions filled for cisapride and troglitazone were analyzed graphically over time as a function of all prescriptions. New prescriptions were defined as those filled by patients who had not received the drug within the previous year. A binomial comparison of the 5 months before and after each safety alert was conducted by Poisson distribution. Overall and new cisapride usage increased after the first alert, which occurred in February 1995 (p<0.05). After the second alert, in September 1995, growth in new prescriptions ended but total prescriptions continued to grow (p<0.05). After the third alert, in June 1998, growth in total use ended and the number of new prescriptions declined (p<0.05). The final two alerts (June 1999 and January 2000) were met with significant declines (p<0.05 for both). Troglitazone was the subject of two alerts in October and December 1997. After these, overall usage increased (p<0.05), whereas the number o new prescriptions decreased (p<0.05). The third alert, in July 1998, caused no change as total prescription use continued to grow (p<0.05), whereas the number of new prescriptions decreased (p<0.05). A fourth alert, in June 1999, resulted in a decrease of overall usage and new prescriptions (p<0.05 for both).
CONCLUSION: Numerous safety alerts were required for each drug before drug usage declined. The decline in overall use was slower than the decline in new prescriptions, possibly indicating a need for increased assessment of refilled prescriptions after the release of new safety data.

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Year:  2004        PMID: 15338846     DOI: 10.1592/phco.24.11.978.36136

Source DB:  PubMed          Journal:  Pharmacotherapy        ISSN: 0277-0008            Impact factor:   4.705


  13 in total

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9.  Stimulated reporting: the impact of US food and drug administration-issued alerts on the adverse event reporting system (FAERS).

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10.  Quantitative Evaluation of Compliance with Recommendation for Sulfonylurea Dose Co-Administered with DPP-4 Inhibitors in Japan.

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