43 results
Keyword Aloxi Remove keyword
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Human medicine European public assessment report (EPAR): Aloxi
palonosetron hydrochloride, Vomiting; Cancer
Date of authorisation: 22/03/2005, Revision: 22, Authorised, Last updated: 24/02/2023Aloxi Signs and Symptoms, Digestive Signs … Aloxi … summary for the public Aloxi palonosetron This is a … -
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Human medicine European public assessment report (EPAR): Palonosetron Accord
Palonosetron, Vomiting; Nausea; Cancer
Date of authorisation: 26/05/2016,
, Revision: 5, Authorised, Last updated: 13/01/2022
European Union (EU) called Aloxi. How is Palonosetron Accord … as the reference medicine, Aloxi. What are the benefits and … shown to be comparable to Aloxi. Therefore, the CHMP’s view … -
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News: Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 19-22 January 2015
CHMP, Last updated: 23/01/2015Aloxi … -
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Press release: European Medicines Agency: Committee for Medicinal Products for Human Use 13-15 December 2004
Last updated: 16/12/2004Aloxi … authorisation applications for: � Aloxi (palonosetron), from Helsinn … -
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Human medicine European public assessment report (EPAR): Akynzeo
netupitant, palonosetron hydrochloride, Vomiting; Neoplasms; Nausea; Cancer
Date of authorisation: 27/05/2015, Revision: 15, Authorised, Last updated: 20/02/2023 -
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Human medicine European public assessment report (EPAR): Palonosetron Hospira
palonosetron hydrochloride, Nausea; Vomiting; Cancer
Date of authorisation: 08/04/2016,, Revision: 4, Withdrawn, Last updated: 08/04/2022
is a generic medicine of Aloxi. There are other generic medicinal … generic medicinal products of Aloxi authorised and marketed … -
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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): 19-22 January 2015
European Medicines Agency, London, UK, from 19/01/2015 to 22/01/2015, Last updated: 03/01/2014 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 3-6 February 2014
European Medicines Agency, London, UK, from 03/02/2014 to 06/02/2014, Last updated: 13/08/2013 -
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Committee for Medicinal Products for Human Use (CHMP): 22-25 September 2014
European Medicines Agency, London, UK, from 22/09/2014 to 25/09/2014, Last updated: 09/08/2013 -
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Committee for Medicinal Products for Human Use (CHMP): 15-18 December 2014
European Medicines Agency, London, UK, from 15/12/2014 to 18/12/2014, Last updated: 09/08/2013 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 6-9 March 2017
European Medicines Agency, London, UK, from 06/03/2017 to 09/03/2017, Last updated: 06/03/2017 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 8-11 September 2014
European Medicines Agency, London, UK, from 08/09/2014 to 11/09/2014, Last updated: 13/08/2013 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 1-4 December 2014
European Medicines Agency, London, UK, from 01/12/2014 to 04/12/2014, Last updated: 13/08/2013 -
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CHMP: Agendas, minutes and highlights (updated)
Last updated: 06/06/2023 -
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Sampling and testing
Last updated: 28/03/2019 -
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Download medicine data
Last updated: 02/12/2021 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 13-16 March 2023
European Medicines Agency, Amsterdam, the Netherlands, from 13/03/2023 to 16/03/2023, Last updated: 18/08/2021 -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 13 - 16 March 2023
PRAC, Last updated: 17/03/2023 -
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Committee for Medicinal Products for Human Use (CHMP): 14-17 September 2020
Virtual meeting, from 14/09/2020 to 17/09/2020, Last updated: 10/03/2021 -
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PRAC: Agendas, minutes and highlights (updated)
Last updated: 07/06/2023 -
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PRAC: Committee agendas, minutes and meeting highlights report archive 2012-2013
Last updated: 01/01/2015 -
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PRAC: meeting archive 2012-2014
Last updated: 13/05/2016 -
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Annual reports and work programmes (updated)
Last updated: 15/05/2023 -
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CHMP: meeting archive 2013-2015
Last updated: 12/05/2016