Results 31 to 40 of about 41 (41)

Comparative bioequivalence study of Pioglitazone tablets, 20 mg (JSC «Chimpharm», Kazakhstan) and Actos® Tablets, 30 mg («Eli Lilly Holdings, Takeda Global Research and Development Centre Europe Ltd»)

open access: yesФармакокинетика и Фармакодинамика, 2013
Within the cross, a single, open, randomized study with a two-week washout period, the two sequences has been studied bioequivalence of tablet forms two pioglitazone 18 volunteers (30 mg dosage).
A. K. Sariev   +8 more
doaj  

Статистический анализ данных исследований биоэквивалентности

open access: yesФармакокинетика и Фармакодинамика, 2020
Появление большого количества генерических лекарственных препаратов объясняет всё вырастающий интерес к проблеме биоэквивалентности, планированию и статистическому анализу данных исследований, проводимых для и установления биоэквивалентности ...

doaj  

Problems of bioanalytical part of bioequivalence studies of drugs in Russia

open access: yesФармакокинетика и Фармакодинамика, 2014
In the review of the main problems holding bioanalytical part of bioequivalence studies of medicines in Russia. The analysis of the major causes of failure when performing studies of bioequivalence and pharmacokinetics.
A. L. Khokhlov   +5 more
doaj  

Peculiarities of approaches to assessing the interchangeability of antiepileptic drugs

open access: yesБезопасность и риск фармакотерапии, 2018
The adequacy of the interchangeability of original and generic drugs is an important economic and social problem in healthcare. In this article we look at the problem of the replacement of antiepileptic drugs.
E. O. Zhuravleva   +2 more
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On the interchangeability of calcineurine inhibitors

open access: yesБезопасность и риск фармакотерапии, 2018
Calcineurin inhibitors, cyclosporine and tacrolimus, are the main immunosuppressants used in solid organ transplantation, but the peculiarities of their pharmacokinetics allow to classify them to a group of medicines with a narrow therapeutic range ...
K. E. Zatolochina   +6 more
doaj  

Interchangeability of levothyroxine sodium tablets

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2018
The article reviews scientific literature and regulatory documents on safe and efficacious use of levothyroxine medicines. Levothyroxine has less than a twofold difference between the minimal toxic concentration and minimal effective concentration.
G. I. Gorodetskaya   +5 more
doaj  

Interchangeability of glibenclamide-containing drugs

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2018
The article analyses the problem of interchangeability of glibenclamide-containing drugs that sometimes lack therapeutic equivalence even though their bioequivalence has been proven.
G. I. Gorodetskaya   +8 more
doaj  

Comparative study of perindopril and perindopril metabolite pharmacokinetics using the HPLC/MS method

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2018
Perindopril is a prodrug which is converted to an active metabolite perindoprilat in the human organism. The present study led to the development of a fast and easily reproducible procedure for simultaneous detection of perinoprilat and its metabolite in
L. M. Krasnykh   +5 more
doaj  

Recommendations on the procedure for determining the interchangeability of medicinal products

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2018
The authors developed and presented recommendations on the procedure for determining the interchangeability of medicinal products. Interchangeability of drugs determined at the state registration of the medicinal product or when amendments to the ...
B. K. Romanov   +12 more
doaj  

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