2022
DOI: 10.3390/healthcare10081392
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Bioequivalence, Drugs with Narrow Therapeutic Index and the Phenomenon of Biocreep: A Critical Analysis of the System for Generic Substitution

Abstract: The prescription of generic drugs represents one of the main cost-containment strategies of health systems, aimed at reducing pharmaceutical expenditure. In this context, most regulatory authorities encourage or obligate dispensing generic drugs because they are far less expensive than their brand-name alternatives. However, drug substitution can be critical in particular situations, such as the use of drugs with a narrow therapeutic index (NTI). Moreover, generics cannot automatically be considered bioequival… Show more

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Cited by 8 publications
(15 citation statements)
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“…Other explanations for variable concentrations could include owner noncompliance (including diet changes) or a change in drug manufacturing during the trial. When switching from 1 generic medication to another as much as a 40% difference in bioavailability can be observed for drugs not considered to be narrow therapeutic index drugs 43 . Given the lack of significant differences in ASD concentrations between CBD and placebo, these variations in ASD concentrations may reflect a normal change seen with ASD administration in dogs.…”
Section: Discussionmentioning
confidence: 99%
“…Other explanations for variable concentrations could include owner noncompliance (including diet changes) or a change in drug manufacturing during the trial. When switching from 1 generic medication to another as much as a 40% difference in bioavailability can be observed for drugs not considered to be narrow therapeutic index drugs 43 . Given the lack of significant differences in ASD concentrations between CBD and placebo, these variations in ASD concentrations may reflect a normal change seen with ASD administration in dogs.…”
Section: Discussionmentioning
confidence: 99%
“…A uniform questionnaire was developed after an extensive literature review. [23][24][25] Initially piloted on 10 pharmacists, unclear questions or duplicates were modified or deleted. The instrumentation's adequacy was assessed as recommended for pilot studies.…”
Section: Data Collectionmentioning
confidence: 99%
“…16 Nevertheless, this involves substituting the same chemical or biological entity at the exact dosage and pharmaceutical form with another product, presenting the same quality, efficacy, and safety profiles. 1,6 Once the marketing authorization file of a generic drug has been accepted, the national regulatory authority can register it, which allows doctors to prescribe it and pharmacists to consider it for substitution. 17,18 The bioequivalence studies guarantee the efficacy of a generic drug identical to that of the originator, but its tolerance may be different due to the disparity of excipients with known effects.…”
Section: Overview Of Generic Drug Substitutionmentioning
confidence: 99%
“…For example, some drugs have a narrow therapeutic index, which means that small dose or concentration changes can significantly impact the drug's effectiveness or safety. 6 In these cases, a healthcare provider may prefer to use the brand-name medication to ensure precise dosing. 7 Most recently, the coronavirus disease pandemic and the corresponding economic impact induced a lack of access to essential drugs, which encouraged the costeffective prescription of substitutes.…”
Section: Introductionmentioning
confidence: 99%