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- W1963897169 abstract "<h3>To the Editor.—</h3> Dr. Lagos aptly describes a phenomenon that has plagued pharmacists for years, that being the proliferation of drug dosage forms and strengths that are of questionable or no clinical usefulness. However, I oppose Dr. Lagos' suggestion that diphenylhydantoin (Dilantin suspension) (125 mg/5 ml) be discontinued by the manufacturer. It enjoys some use in adult, hospitalized patients in whom the solid dosage form is not indicated. I agree that inadvertent dispensing of the stronger suspension for the weaker one may lead to intoxication, just as it would for many drugs available in different strengths. Obviously, the resolution of this problem lies in the continuing education of pharmacists and physicians (and manufacturers) that will help to inform them of these problems. Hospital pharmacists are continually challenged by orders for liquid preparations when none exist on the commercial market. It is no easy matter to formulate and prepare extemporaneous suspensions" @default.
- W1963897169 created "2016-06-24" @default.
- W1963897169 creator A5084731950 @default.
- W1963897169 date "1972-07-03" @default.
- W1963897169 modified "2023-09-27" @default.
- W1963897169 title "Diphenylhydantoin Suspension Hazard" @default.
- W1963897169 doi "https://doi.org/10.1001/jama.1972.03200140073033" @default.
- W1963897169 hasPublicationYear "1972" @default.
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