Results 11 to 20 of about 3,107,552 (340)

Dissolution test for oral suspension: an overview about use and importance

open access: yesBrazilian Journal of Pharmaceutical Sciences, 2022
This work aims to ascertain the comprehensiveness of dissolution tests for oral suspensions registered in Brazil and the USA. After consulting literature since 1994, a paucity of information about dissolution methods for suspensions was detected.
Thaís dos Santos Paulino Soares   +3 more
doaj   +1 more source

Therapeutic Equivalence Evaluated Through In Vitro Studies of Multi-Source Drugs: A Moxifloxacin Case Study in Lima, Peru

open access: yesDissolution Technologies, 2022
This study aimed to determine the therapeutic equivalence of four multi-source drugs containing moxifloxacin (400 mg tablets) in vitro studies to establish their interchangeability with the reference product.
V. Chumpitaz-Cerrate   +5 more
semanticscholar   +1 more source

Comparison of Efficacy and Safety of Lupin’s Pegfilgrastim with Neulastim® as an Adjunct to Chemotherapy in Patients with Non Myeloid Malignancies: A Randomised Phase III Clinical Study [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2022
Introduction: Pegfilgrastim is indicated in patients receiving myelosuppressive anticancer drugs to reduce the Duration of Severe Neutropenia (DSN) and incidence of Febrile Neutropenia (FN).
Minish Jain   +6 more
doaj   +1 more source

Determination of therapeutic equivalence of generic products of gentamicin in the neutropenic mouse thigh infection model. [PDF]

open access: yesPLoS ONE, 2010
BackgroundDrug regulatory agencies (DRA) support prescription of generic products of intravenous antibiotics assuming therapeutic equivalence from pharmaceutical equivalence.
Andres F Zuluaga   +4 more
doaj   +1 more source

Dried blood spot: Utilizing dry blood for pharmacokinetic investigations - an old method with great future for therapeutic drug monitoring [PDF]

open access: yesVojnosanitetski Pregled, 2018
nema
Goločorbin-Kon Svetlana   +4 more
doaj   +1 more source

In Vitro Therapeutic Equivalence of Two Multisource (Generic) Formulations of Sodium Phenytoin (100 mg) Available in Peru

open access: yesDissolution Technologies, 2020
( 13 ). An f 2 value of exactly 100 means that the profile of the generic drug is identical to the reference; if the value is 50–99, then the profiles are similar ( 10, 12, ABSTRACT This in vitro study evaluated the therapeutic equivalence of two ...
Angel T. Alvarado   +9 more
semanticscholar   +1 more source

Efficacy and safety of a switch from twice-daily tacrolimus to once-daily generic tacrolimus in stable liver transplant patients

open access: yesKorean Journal of Transplantation, 2021
Background : Once-daily tacrolimus reduces non-compliance relative to twice-daily tacrolimus. However, little is known about the safety and efficacy of conversion from twice-daily tacrolimus to generic once-daily tacrolimus in liver transplantation (LT).
Jong Man Kim   +17 more
doaj   +1 more source

The choice of gadolinium-based contrast agents: a radiologist’s responsibility between pharmaceutical equivalence and bioethical issues [PDF]

open access: yes, 2017
Contrast Agents (CA) are among the most commonly prescribed drugs worldwide, and are used, with a variety of techniques, to increase and intensify the differences between body tissues and to help radiologist make diagnoses in a fast and precise way.
Cartocci, Gaia   +5 more
core   +2 more sources

Training Programme Impact in Improving the Working Memory of Students with Learning Disabilities in Reading Arabic [PDF]

open access: yes, 2020
The study aimed to investigate the effect of a training program on improving working memory for students with learning difficulties in reading Arabic. The study sample consisted of (10) students with learning disabilities from Basic Education students ...
Aljundi, K. M. (Khalid)
core   +3 more sources

WHAT IS THERAPEUTIC EQUIVALENCE OF GENERIC DRUG AND HOW TO PROVE IT

open access: yesРациональная фармакотерапия в кардиологии, 2016
The problem of generic drugs use in clinical practice and confirmation of their therapeutic equivalence is discussed. The significance of studies on generic drugs bioequivalence, as well as details of international practice and regulations in this area ...
N. P. Kutishenko   +2 more
doaj   +1 more source

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