Sugar content in liquid oral medicines for children

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A multidisciplinary audit examining the prescribing of sugar free liquid medicines to children in South Tyneside

Th e au th or s Claire Kelly, BA, is clinical audit, research and development facilitator, Mark Burdon, BSc, MRPharmS, is community pharmacy development and clinical governance facilitator, Anne Archer, is dental health facilitator, Kathryn Featherstone, BSc, MRPharmS, is head of medicines management and Pam Lee, MPH, is public health specialist at South Tyneside Primary Care Trust. David Carte...

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Medicines for children: flexible solid oral formulations

Perspectives Children younger than five years old are generally unable to safely swallow solid capsules and tablets larger than 10 mm. 1 Although oral liquid medicines can be prescribed, these have some disadvantages over solid medicines. Substances or excipients that solubilize the active ingredient or ensure microbial stability are included in oral liquids and these may be harmful to young ch...

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Sucrose concentration and pH in liquid oral pediatric medicines of long-term use for children.

OBJECTIVES To determine the pH and sucrose concentrations (SC) of pediatric liquid drugs of long-term use by children in order to evaluate the potential risk for dental caries and dental erosion. METHODS After assessing the pH, we analyzed 71 aqueous medicine samples for sucrose by the Lane-Eynon general volumetric method. The pH and SC values (mean +/- standard deviation (SD) were calculated...

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Cariogenic Potential of Most Commonly Prescribed Liquid Oral Medicines for Children

Consumption of liquid oral medicine by frequently ill children, significantly increases the risk of tooth demineralization. In this study a survey was conducted wherein the pediatricians, pharmacist and medical representatives of Bhopal city were enquired about the most commonly prescribed liquid oral medicines for children. The four categories of medicines reported were: antipyretics/analgesic...

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Oral Medicines for Children in the European Paediatric Investigation Plans

INTRODUCTION Pharmaceutical industry is no longer allowed to develop new medicines for use in adults only, as the 2007 Paediatric Regulation requires children to be considered also. The plans for such paediatric development called Paediatric Investigation Plans (PIPs) are subject to agreement by the European Medicines Agency (EMA) and its Paediatric Committee (PDCO). The aim of this study was t...

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ژورنال

عنوان ژورنال: Revista de Saúde Pública

سال: 2005

ISSN: 0034-8910

DOI: 10.1590/s0034-89102005000300022