2015
DOI: 10.4088/jcp.15f10300
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Bioequivalence of Generic Drugs

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Cited by 19 publications
(18 citation statements)
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“…Generic medications provide a lower cost option. However, even though approval of a generic medication requires a demonstration of bioequivalence, which does sometimes fail ( Chenu et al, 2009 ; Woodcock et al, 2012 ), there nonetheless may be efficacy or tolerability differences for some patients taking generic drugs, possibly related to difference in excipients ( Gallelli et al, 2013 ; Andrade, 2015 ). Discussing insurance coverage may inform antidepressant selection, as restrictions and higher copay requirements may preclude patients from following through with their prescription.…”
Section: How Does the Clinician Provide Early Optimized Treatment Formentioning
confidence: 99%
“…Generic medications provide a lower cost option. However, even though approval of a generic medication requires a demonstration of bioequivalence, which does sometimes fail ( Chenu et al, 2009 ; Woodcock et al, 2012 ), there nonetheless may be efficacy or tolerability differences for some patients taking generic drugs, possibly related to difference in excipients ( Gallelli et al, 2013 ; Andrade, 2015 ). Discussing insurance coverage may inform antidepressant selection, as restrictions and higher copay requirements may preclude patients from following through with their prescription.…”
Section: How Does the Clinician Provide Early Optimized Treatment Formentioning
confidence: 99%
“…There is evidence to suggest that generic medicines are as good as branded medicines with regard to bioequivalence and therapeutic equivalence. [10][11][12] Few prescriptions were irrational like gastritis, acute gastroentereitis, enteric fever, malaria, organophosphorus poisoning and bronchopneumonia. The irrational use of prescriptions will not only promote health problems can also be linked to adverse effects, high cost, drug interactions and emergence of drug resistance, especially in antimicrobial therapy.…”
Section: Resultsmentioning
confidence: 99%
“…This can create problem for drugs with narrow therapeutic index [26]. According to the Adrade [27], this is because bioequivalent brands of drugs may differ in their excipient content, which can result in variations in safety profiles. In our study, vast majority of the participants emphasized the therapeutic equivalence of the drug for their preferences.…”
Section: Discussionmentioning
confidence: 99%