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Questions and answers on the review of prozac for use in children and adolescents

QUESTIONS AND ANSWERS ON THE REVIEW OF PROZAC
FOR USE IN CHILDREN AND ADOLESCENTS

The Committee for Medicinal Products for Human Use (CHMP) has completed its arbitration review
of Prozac (fluoxetine) and associated namesextend its use in the
treatment of children suffering from depression, provided that the marketing authorisation holder
(MAH), Eli Lilly, carries out additional studies to ensure that the safety profile of Prozac remains
acceptable. The new indication is as follows:
Children and adolescents aged 8 years and above: Moderate to severe major depressive episode, if
depression is unresponsive to psychological therapy after 4-6 sessions. Antidepressant medication
should be offered to a child or young person with moderate to severe depression only in combination
with a concurrent psychological therapy.

Why did the CHMP review this medicine?
Prozac is currently authorised for use in adults to treat depression, obsessive-compulsive disorders and
bulimia nervosa (an eating disorder) within the European Union.
Following a request from the UK, the MAH for Prozac submitted an application for the extension of
the indications to treat depression in children and adolescents, via the mutual recognition procedureThe review was initiated by France on the basis of safety and efficacy concerns on the use of Prozac in
this age group.
What data has the CHMP reviewed?
The CHMP reviewed data submitted by the MAH, which included data from experimental models,
clinical studies and information published in scientific journals.
Efficacy was supported by three main studies, involving over 750 children and adolescents. All studies
compared the efficacy of Prozac in the treatment of depression with that of a placebo (dummy
treatment) over 9 to 12 weeks. The CHMP also reviewed safety data from experimental and clinical
studies on growth, sexual development and suicide-related behaviour (suicide attempt and suicidal
thoughts).
What are the conclusions of the CHMP?
• The studies in children and adolescents showed a positive effect. • The medicine should only be used together with psychological therapy in patients non- responding to such therapy alone after 4 to 6 sessions. • The starting dose should be 10 mg per day (given as 2.5ml of the oral solution) and it may be increased to 20 mg per day after one to two weeks. • If no clinical benefit is seen within 9 weeks, treatment should be reconsidered. • The significance of the observations in experimental studies on sexual development, emotional behaviour and testicular toxicity will be further investigated. The MAH will also put in place a system to obtain safety data in treated children, in particular regarding sexual development. • The CHMP confirmed that doctors and parents should carefully monitor children and adolescents for suicidal behaviour, particularly at the beginning of treatment. 1 Prozac is marketed also under the names of Fluctin, Fluctine, Fluoxétine Lilly, Fluoxétine RPG Prozac, Fontex, Ladose. 2 This is a procedure whereby Member States mutually recognise marketing authorisations within the European Union. In case of disagreement during the procedure, the issue is referred to the CHMP for arbitration. 7 Westferry Circus, Canary Wharf, London E14 4HB, UK Tel. (44-20) 74 18 84 00 Fax (44-20) 74 18 84 16 E-mail: mail@emea.eu.int http://www.emea.eu.int EMEA 2006 Reproduction and/or distribution of this document is authorised for non commercial purposes only provided the EMEA is acknowledged Overall, the CHMP concluded that the benefits of Prozac are greater than its potential risks for the treatment of moderate to severe major depressive episode in children and adolescents. For further information, please refer to the Product Information for Prozac as adopted by the CHMP on 1 June 2006. The document is published for information on the EMEA website, pending formal endorsement by the European Commission, and can be found.

Source: http://www.trouw.nl/static/nmc/nmc/redactie/Prozac_children_decision_EMA.pdf

Microsoft word - gores.therakos.closingpressrelease.final

FOR IMMEDIATE RELEASE THE GORES GROUP COMPLETES THE ACQUISITION OF THERAKOS, INC. FROM ORTHO-CLINICAL DIAGNOSTICS, INC.   LOS ANGELES, JANUARY 2, 2013 – The Gores Group, a global investment firm focused on acquiring controlling interests in mature and growing businesses, today announced that it has completed the acquisition of Therakos, Inc. from Ortho-Clinical Diagnostics, Inc

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AGGIORNAMENTI WHO DRUG INFORMATION è una pubblicazione trimestrale dell’Organizzazio-ne Mondiale della Sanità (OMS). Tra gli obiettivi che si propone, vi è quello di for-nire valutazioni su temi farmacologico-clinici di particolare rilevanza e raccoman-dazioni per un corretto impiego dei farmaci. Nella rubrica “Reports on IndividualDrugs” del Volume 13 n. 1 del 1999 sono, tra l’altr

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