44 results
Keyword Eporatio Remove keyword
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Human medicine European public assessment report (EPAR): Eporatio
epoetin theta, Kidney Failure, Chronic; Anemia; Cancer
Date of authorisation: 29/10/2009, Revision: 13, Authorised, Last updated: 27/09/2023Eporatio Female Urogenital Diseases Female … part of the EPAR). What is Eporatio? Eporatio is a solution for injection … substance, epoetin theta. What is Eporatio used for Eporatio is used to treat anaemia … -
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Withdrawn application: Ratioepo
epoetin theta, date of withdrawal: 25/02/2010, Initial authorisation, Last updated: 22/03/2010theta containing medicines Eporatio and Biopoin. The Committee … be able to receive either Eporatio or Biopoin, both of which … application does not affect Eporatio and Biopin, which were part … -
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Human medicine European public assessment report (EPAR): Vafseo
Vadadustat, Renal Insufficiency, Chronic; Anemia
Date of authorisation: 24/04/2023,
, Authorised, Last updated: 31/05/2023
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Pharmacovigilance Risk Assessment Committee (PRAC): 29 November-2 December 2021
European Medicines Agency, Amsterdam, the Netherlands, from 29/11/2021 to 02/12/2021, Last updated: 04/10/2022 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 4-7 February 2013
European Medicines Agency, London, UK, from 04/02/2013 to 07/02/2013, Last updated: 02/06/2012 -
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Committee for Medicinal Products for Human Use (CHMP): 16-19 December 2013
European Medicines Agency, London, UK, from 16/12/2013 to 19/12/2013, Last updated: 09/07/2012 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 30 November-3 December 2015
European Medicines Agency, London, UK, from 30/11/2015 to 03/12/2015, Last updated: 13/03/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 9-12 February 2015
European Medicines Agency, London, UK, from 09/02/2015 to 12/02/2015, Last updated: 13/03/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 9-12 March 2015
European Medicines Agency, London, UK, from 09/03/2015 to 12/03/2015, Last updated: 13/03/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 7-10 July 2014
European Medicines Agency, London, UK, from 07/07/2014 to 10/07/2014, Last updated: 13/08/2013 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 6-9 January 2014
European Medicines Agency, London, UK, from 06/01/2014 to 09/01/2014, Last updated: 13/08/2013 -
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PRAC: Committee agendas, minutes and meeting highlights report archive 2012-2013
Last updated: 01/01/2015 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 2-5 December 2013
European Medicines Agency, London, UK, from 02/12/2013 to 05/12/2013, Last updated: 02/07/2012 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 7-10 October 2013
European Medicines Agency, London, UK, from 07/10/2013 to 10/10/2013, Last updated: 02/07/2012 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 6-9 February 2017
European Medicines Agency, London, UK, from 06/02/2017 to 09/02/2017, Last updated: 13/03/2014 -
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Press release: European Medicines Agency now publishing meeting agendas for all scientific committees
Last updated: 17/12/2013 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 3-6 July 2017
European Medicines Agency, London, UK, from 03/07/2017 to 06/07/2017, Last updated: 13/03/2014 -
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PRAC: Agendas, minutes and highlights (updated)
Last updated: 30/11/2023 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 13-16 May 2013
European Medicines Agency, London, UK, from 13/05/2013 to 16/05/2013, Last updated: 02/07/2012 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 8-11 April 2013
European Medicines Agency, London, UK, from 08/04/2013 to 11/04/2013, Last updated: 02/06/2012 -
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PRAC: meeting archive 2012-2014
Last updated: 13/05/2016 -
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PRAC recommendations on safety signals (updated)
Last updated: 20/11/2023 -
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News: European Medicines Agency publishes minutes of CHMP, CVMP and CAT meetings for the first time
Last updated: 28/01/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 8-11 June 2015
European Medicines Agency, London, UK, from 08/06/2015 to 11/06/2015, Last updated: 13/03/2014 -
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Committee for Medicinal Products for Human Use (CHMP): 17-20 July 2017
European Medicines Agency, London, UK, from 17/07/2017 to 20/07/2017, Last updated: 06/01/2014