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hexal medicine

Orlistat is for use only in adults that are overweight or obese. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Methylphenidate is a medicine that is used to treat children aged between six and 18 years of age who have attention-deficit / hyperactivity disorder (ADHD), a condition in which children show a persistent inability to concentrate, hyperactivity and impulsive behaviour. Filgrastim Hexal is usually given in a specialised treatment centre, although patients who receive it by injection under the skin may inject themselves once they have been trained appropriately. A list of US medications equivalent to Tramadol Retard Hexal is available on the Drugs.com website. Changes since initial authorisation of medicine, Initial marketing-authorisation documents, Committee for Medicinal Products for Human Use, International non-proprietary name (INN) or common name, Anatomical therapeutic chemical (ATC) code, Date of issue of marketing authorisation valid throughout the European Union. L484, You may also search by drug name or NDC code. 09/02/2012 Clopidogrel Hexal - EMEA/H/C/001139 - A20/0006. Cetirizine is an antihistamine that reduces the natural chemical histamine in the body. Cetirizin HEXAL may be available in the countries listed below. The European Commission issued a decision on this opinion on 09 October 2013. Methylphenidate belongs to a group of medicines called 'psychostimulants' and is thought to work by enhancing the activity of areas of the brain that control attention and concentration. The United Kingdom (UK) withdrew from the European Union (EU) on 31 January 2020 and is no longer an EU Member State. 5,67 EUR / approx. For the full list of all side effects reported with Filgrastim Hexal, see the package leaflet. As the product information states that the tablet can be taken with or without food, a bioequivalence study in fed conditions was required to grant the marketing authorisation. Filgrastim Hexal is a ‘biosimilar medicine'. The active substance in Filgrastim Hexal, filgrastim, is very similar to a human protein called granulocyte colony stimulating factor (G-CSF). Useful tip: Search for the imprint first, then refine by color and shape if you have too many results. Consult with your healthcare professional before taking any medication. The marketing authorisation for Clopidogrel Hexal has been withdrawn at the request of the marketing-authorisation holder. The studies looked at the effects of single and repeated administration of various doses of the medicines, either injected under the skin or infused into a vein. Changes since initial authorisation of medicine, Initial marketing-authorisation documents, International non-proprietary name (INN) or common name, Anatomical therapeutic chemical (ATC) code, Date of issue of marketing authorisation valid throughout the European Union, Annex I - Summary of product characteristics, Annex IIA - Manufacturing-authorisation holder responsible for batch release, Annex IIB - Conditions of the marketing authorisation. You are therefore advised to be selective about which sections or pages you wish to print. Methotrexate is reported as an ingredient of MTX Hexal in the following countries: Methotrexate sodium (a derivative of Methotrexate) is reported as an ingredient of MTX Hexal in the following countries: Important Notice: The Drugs.com international database is in BETA release. This is a summary of the European public assessment report (EPAR). Filgrastim Hexal is given by injection under the skin or infusion into a vein. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR). This medicine must be used together with a reduced-calorie diet and increased physical activity. For informational purposes and non-commercial usage only. To all offered drugs and other appliances the pharmaceutical staff of the BENNEWITZ DRUGS DIVISION gives advice. Hexalen, Hexadrol, Exalgo. Data sources include IBM Watson Micromedex (updated 1 Oct 2020), Cerner Multum™ (updated 1 Oct 2020), Wolters Kluwer™ (updated 30 Sep 2020) and others. EMA is in the process of making appropriate changes to this website. Committee for Medicinal Products for Human Use, International non-proprietary name (INN) or common name, Questions and answers (Q&A) - easy-to-understand summary of key issues and Committee conclusions, Scientific conclusions of the Committee (Annex II). The United Kingdom (UK) withdrew from the European Union (EU) on 31 January 2020 and is no longer an EU Member State.

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