29 results
Keyword Ketamina Molteni Remove keyword
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Human medicine European public assessment report (EPAR): Sixmo
Buprenorphine hydrochloride, Opioid-Related Disorders
Date of authorisation: 19/06/2019,
, Revision: 3, Authorised, Last updated: 04/01/2022
Marketing-authorisation holder L. Molteni & C. dei Fratelli Alitti … -
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National expert: Giuseppe Capovilla, Italian Medicines Agency (updated)
- Declaration of interests - 79.91 KB | PDF
- Curriculum Vitae - 33.67 KB | PDF
S, RENZETTI V, SALVONI L, MOLTENI M, SALANDI A, TRABATTONI … S, RENZETTI V, SALVONI L, MOLTENI M, SALANDI A, TRABATTONI … -
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Press release: New long-lasting implant to treat opioid dependence
Last updated: 26/04/2019The applicant for Sixmo is L. Molteni & C. dei Fratelli Alitti … -
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National expert: Paola Minghetti, Italian Medicines Agency (updated)
- Declaration of interests - 81.41 KB | PDF
- Curriculum Vitae - 62.13 KB | PDF
myeloma 10/2011-(current) Molteni medical devices 12/2011-(current … -
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Human medicine European public assessment report (EPAR): Rizmoic
Naldemedine tosilate, Constipation
Date of authorisation: 18/02/2019,, Revision: 6, Authorised, Last updated: 10/01/2022
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Human medicine European public assessment report (EPAR): PecFent
fentanyl, Pain; Cancer
Date of authorisation: 31/08/2010, Revision: 22, Authorised, Last updated: 01/06/2022 -
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National expert: Anna Kajaste-Rudnitski, Italian Medicines Agency (updated)
- Declaration of interests - 80.46 KB | PDF
- Curriculum Vitae - 29.18 KB | PDF
corresponding author. 2. Molteni R, Biavasco R, Stefanoni … -
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National expert: Francesco Onida, Italian Medicines Agency (updated)
- Declaration of interests - 81.89 KB | PDF
- Curriculum Vitae - 50.99 KB | PDF
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News: Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 23-26 April 2019
CHMP, Last updated: 26/04/2019Marketing-authorisation applicant L. Molteni & C. dei Fratelli Alitti … -
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Referral: Nimesulide
nimesulide, Article 31 referrals
Status: European Commission final decision, opinion/position date: 18/12/2003, EC decision date: 26/04/2004, Last updated: 13/05/2004 -
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Referral: Modified-released oral opioids
hydromorphone, morphine, oxycodone, Article 31 referrals
Status: European Commission final decision, opinion/position date: 18/11/2010, EC decision date: 20/04/2011, Last updated: 06/06/2011 -
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Referral: Calcitonins
calcitonin, Article 31 referrals
Status: European Commission final decision, opinion/position date: 22/11/2002, EC decision date: 12/06/2003, Last updated: 02/03/2004Vial (12 doses) 1 Italy Molteni Farmaceutici L Molteni E C. Dei F .Lli Alitti Societa' … -
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Referral: Serotonin-specific reuptake inhibitors and serotonin-noradrenaline reuptake inhibitors
atomoxetine, citalopram, escitalopram, fluoxetine, fluvoxamine, mianserine, milnacipran, mirtazapine, paroxetine, reboxetine, sertraline, venlafaxine, Article 31 referrals
Status: European Commission final decision, opinion/position date: 21/04/2005, EC decision date: 19/08/2005, Last updated: 03/11/2005 -
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Referral: Ibuprofen- and dexibuprofen-containing medicines
ibuprofen, dexibuprofen, Article 31 referrals
Status: CMDh final position, opinion/position date: 20/05/2015, Last updated: 14/07/2015 -
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Public data from Article 57 database (updated)
Last updated: 27/09/2022 -
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List of medicines under additional monitoring (updated)
Last updated: 28/09/2022 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 7-10 June 2022
European Medicines Agency, Amsterdam, the Netherlands, from 07/06/2022 to 10/06/2022, Last updated: 07/06/2022 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 28 September-1 October 2020
Virtual meeting, from 28/09/2020 to 01/10/2020, Last updated: 29/09/2020 -
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PRAC: Agendas, minutes and highlights (updated)
Last updated: 04/10/2022 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 7-10 June 2021
European Medicines Agency, Amsterdam, the Netherlands, from 07/06/2021 to 10/06/2021, Last updated: 07/06/2021 -
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EudraVigilance: electronic reporting
Last updated: 15/02/2022 -
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Pharmacovigilance Risk Assessment Committee (PRAC): 11-14 January 2021
Virtual meeting, from 11/01/2021 to 14/01/2021, Last updated: 27/02/2018 -
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Guidance documents
Last updated: 19/07/2022 -
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Reinforcing patient safety in Europe
Zagreb, Croatia, from 14/06/2011 to 15/06/2011, Last updated: 23/06/2011Croatia, Croatia Lino Molteni EU Delegation of Croatia … -
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Pharmacovigilance Risk Assessment Committee (PRAC): 10-13 January 2022
European Medicines Agency, Amsterdam, the Netherlands, from 10/01/2022 to 13/01/2022, Last updated: 21/06/2021