PT  - JOURNAL ARTICLE
AU  - Gavrus Ion, D
AU  - Bossacoma Busquets, F
AU  - Romo Murillo, MA
AU  - Catala Foguet, JM
AU  - Diaz Cambron, A
AU  - Sánchez Celma, M
AU  - Villaronga Flaqué, M
AU  - Cuartero Lozano, JA
AU  - Vinent Genestar, J
AU  - Farre Riba, R
TI  - 5PSQ-094 Use of excipients in oral liquid commercial medicines in a children’s hospital
AID  - 10.1136/ejhpharm-2019-eahpconf.527
DP  - 2019 Mar 01
TA  - European Journal of Hospital Pharmacy
PG  - A245--A245
VI  - 26
IP  - Suppl 1
4099  - http://ejhp.bmj.com/content/26/Suppl_1/A245.1.short
4100  - http://ejhp.bmj.com/content/26/Suppl_1/A245.1.full
SO  - Eur J Hosp Pharm2019 Mar 01; 26
AB  - Background Oral liquid medicines, such as solutions and suspensions, are commonly given to young children, because they are easy to swallow and allow weight-based dosage. The development of oral medicines for paediatric patients often requires age-appropriate formulations which can be more complex and may involve a broader range of excipients than adult dosage forms.Purpose Identify excipients having a potential risk of safety concerns in the paediatric population of commercial oral liquid medicines of our hospital formulary.Material and methods All oral liquid medicines included in the hospital’s drug formulary were reviewed, using components information from the summary product characteristics obtained from the Spanish Medicament Agency (AEMPS1), and compared with the oral excipients from the European Commission guideline on ‘Excipients in the labelling and package leaflet of medicinal products for human use’.2Results We reviewed 96 SPC oral liquid medicines, 16 oral drops and 80 suspensions or solutions, only 12 of which were non-indicated excipients-free.View this table:Abstract 5PSQ-094 Table 1 Bold excipients contraindicated in neonates/children less than 6 years. Italic: contraindicated in patients with metabolic disorders.3Conclusion A high percentage (87%) of liquid medicines in our formulary commonly used to treat children contain potentially harmful excipients. So, specific criteria have to be implemented in the drug procurement process. The use of excipients in paediatric medicines is driven by functional requirements and should be justified through a risk-based assessment, considering, among others, the paediatric age group, frequency of dosing and duration of treatment and excipient concentration. Clinicians should be aware of this in prescribing appropriate treatment in this population. When a commercial medicine contains an excipient that can cause problems in paediatrics, compounding may be an appropriated solution.References and/or acknowledgements 1. AEMPS https://www.aemps.gob.es/cima/publico/home.html2. https://www.ema.europa.eu/documents/scientific-guideline/annex-european-commission-guideline-excipients-labelling-package-leaflet-medicinal-products-human_en.pdf3. Breikreutz J, Boos J. Expert Opin Drug Deliv2007;4:37–45.No conflict of interest.