14 results
Keyword Arcoxia Remove keyword
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Referral: Arcoxia
etoricoxib, Article 6(12) referrals (prior to January 2010)
Status: European Commission final decision, opinion/position date: 26/06/2008, EC decision date: 09/09/2008, Last updated: 21/11/2008Arcoxia … the benefit/risk profile of Arcoxia was needed. The arbitration … Article 6(12) referral for Arcoxia International Non-Proprietary … -
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Referral: Etoricoxib
etoricoxib, Article 31 referrals
Status: European Commission final decision, opinion/position date: 26/06/2008, Last updated: 21/11/2008Etoricoxib is available in Algix, Arcoxia, Auxib, Etoricoxib MSD, Exxiv … etoricoxib-containing medicine Arcoxia is currently being assessed … granted. As the proposed dose of Arcoxia for ankylosing spondylitis … -
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Press release: EMEA recommends strengthening warnings and contraindications for etoricoxib-containing medicines used in the treatment of rheumatoid arthritis and ankylosing spondylitis
CHMP, Last updated: 26/06/2008etoricoxib-containing medicine Arcoxia to treat ankylosing spondylitis … extension of indication for Arcoxia to include ankylosing spondylitis … Regulation EC No 1084/2003, for Arcoxia because of disagreement between … -
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Referral: Etoricoxib
etoricoxib, Article 31 referrals
Status: European Commission final decision, opinion/position date: 23/06/2005, EC decision date: 28/11/2005, Last updated: 06/12/2005 -
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Referral: Etoricoxib
etoricoxib, Article 31 referrals
Status: European Commission final decision, opinion/position date: 27/02/2004, EC decision date: 28/04/2004, Last updated: 09/06/2004A-1220 Wien Austria Arcoxia 60 mg Film-coated tablets … A-1220 Wien Austria Arcoxia 90 mg Film-coated tablets … A-1220 Wien Austria Arcoxia 120 mg Film-coated tablets … -
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Press release: Meeting highlights from the Committee for Medicinal Products for Human Use,23-26 June 2008
CHMP, Last updated: 26/06/2008 -
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Press release: Meeting highlights from the Committee for Medicinal Products for Human Use,17-20 September 2007
CHMP, Last updated: 21/09/2007 -
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News: 2013 annual report on EudraVigilance: over 1 million adverse reaction reports received and processed
Last updated: 28/04/2014 -
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Public data from Article 57 database
Last updated: 17/10/2022 -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 5-8 May 2014
PRAC, Last updated: 08/05/2014 -
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Annual reports and work programmes (updated)
Last updated: 15/05/2023 -
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Press release: EMEA reports strong performance in regulatory and public-health activities in 2007; the outlook for 2008 is even higher application numbers and a focus on advanced-therapy medicines
Last updated: 10/03/2008 -
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EudraVigilance
Last updated: 25/03/2020 -
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CHMP: meeting archive 2001-2009
Last updated: 18/11/2013