Nimenrix powder and solvent for solution for injection in pre-filled syringe
*Company:
Pfizer Healthcare IrelandStatus:
No Recent UpdateLegal Category:
Product subject to medical prescription which may not be renewed (A)Active Ingredient(s):
*Additional information is available within the SPC or upon request to the company
Updated on 16 February 2024
File name
AdvHCPLeafletNI200pfsIENIclean.pdf
Reasons for updating
- Change to section 6 - manufacturer
- Change to section 6 - date of revision
Updated on 19 May 2022
File name
AdvSPCNI200IEclean.pdf
Reasons for updating
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows: section 5.1 to include long-term toddler antibody persistence data from study MenACWY-TT-104.
Updated on 03 March 2022
File name
AdvSPCNI190IEclean.pdf
Reasons for updating
- Change to section 4.8 - Undesirable effects
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows: update to section 4.8 to include 'Urticaria' and 'Febrile Convulsion' as undesirable effects.
Updated on 03 March 2022
File name
AdvHCPLeafletNI190pfsIENIclean.pdf
Reasons for updating
- Change to section 4 - possible side effects
- Change to section 6 - date of revision
Updated on 08 November 2021
File name
Adv HCP Leaflet NI 18_0 pfs IE NI clean.pdf
Reasons for updating
- Change to section 4 - how to report a side effect
- Change to other sources of information section
- Individual PILs superseded by joint PIL
Updated on 25 March 2021
File name
DEC202120551_Adv SPC NI 18_0 IE clean.pdf
Reasons for updating
- Change to section 4.2 - Posology and method of administration
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 25 March 2021
File name
DEC202120551_Adv HCP Leaflet NI 17_0 pfs IE clean.pdf
Reasons for updating
- Change to section 6 - date of revision
- Correction of spelling/typing errors
Updated on 24 February 2021
File name
DEC202111954_Adv SPC NI 17_0 IE clean.pdf
Reasons for updating
- Change to section 4.8 - Undesirable effects
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 24 February 2021
File name
DEC202111954_Adv HCP Leaflet NI 16_0 pfs IE clean.pdf
Reasons for updating
- Change to section 4 - possible side effects
- Change to section 6 - date of revision
Updated on 12 November 2020
File name
DEC202075824_Adv SPC NI 16_0 IE clean.pdf
Reasons for updating
- Change to section 4.4 - Special warnings and precautions for use
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 12 November 2020
File name
DEC202075824_Adv HCP Leaflet NI 15_0 pfs IE clean.pdf
Reasons for updating
- Change to section 2 - excipient warnings
- Change to section 6 - what the product contains
- Change to section 6 - date of revision
Updated on 23 October 2020
File name
Adv SPC NI 15_0 IE clean.pdf
Reasons for updating
- Change to Section 4.8 – Undesirable effects - how to report a side effect
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 23 October 2020
File name
Adv HCP Leaflet NI 14_0 pfs IE clean.pdf
Reasons for updating
- Change to section 4 - how to report a side effect
- Change to MA holder contact details
Updated on 28 February 2020
File name
DEC202012895_Adv SPC NI 14_0 UK IE clean.pdf
Reasons for updating
- Change to section 1 - Name of medicinal product
- Change to section 4.1 - Therapeutic indications
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 28 February 2020
File name
DEC202012895_Adv HCP Leaflet NI 13_0 pfs UK IE clean.pdf
Reasons for updating
- Change to section 2 - interactions with other medicines, food or drink
- Change to section 6 - date of revision
Updated on 27 February 2020
File name
DEC202012644_Adv SPC NI 13_0 UK IE clean.pdf
Reasons for updating
- Change to section 1 - Name of medicinal product
- Change to section 6.5 - Nature and contents of container
- Change to section 6.6 - Special precautions for disposal and other handling
- Change to section 8 - Marketing authorisation number(s)
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 01 April 2019
File name
DEC201916385_Adv HCP Leaflet NI 12_0 pfs UK IE clean.pdf
Reasons for updating
- Change to section 3 - dose and frequency
- Change to section 3 - use in children/adolescents
- Change to section 3 - how to take/use
- Change to section 3 - duration of treatment
- Change to section 3 - overdose, missed or forgotten doses
- Change to section 6 - date of revision
Updated on 01 April 2019
File name
DEC201916385_Adv SPC NI 12_0 UK IE clean.pdf
Reasons for updating
- Change to section 4.2 - Posology and method of administration
- Change to section 4.4 - Special warnings and precautions for use
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 25 January 2019
File name
Adv HCP Leaflet NI 11_0 pfs UK IE clean.pdf
Reasons for updating
- Change to section 6 - date of revision
Updated on 25 January 2019
File name
Adv SPC NI 11_0 UK IE clean.pdf
Reasons for updating
- Change to section 4.4 - Special warnings and precautions for use
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
“Update of section 4.4 of the SmPC in order to add a warning about an increased risk of invasive disease caused by Neisseria meningitidis group A, C, W-135 and Y”.
Updated on 23 October 2018
File name
Adv HCP Leaflet NI 10_0 pfs UK IE clean.pdf
Reasons for updating
- Change to section 6 - date of revision
Updated on 19 October 2018
File name
Adv SPC NI 10_0 UK IE clean.pdf
Reasons for updating
- Change to section 6.3 - Shelf life
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows: Section 6.3 is updated with the new shelf-life.
Updated on 08 August 2018
File name
Adv HCP Leaflet NI 9_0 pfs UK IE clean.pdf
Reasons for updating
- Change to section 6 - marketing authorisation holder
- Change to section 6 - date of revision
Updated on 08 August 2018
File name
Adv SPC NI 9_0 UK IE clean.pdf
Reasons for updating
- Change to section 7 - Marketing authorisation holder
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows|;
SECTION 7 – Change to MAH
SECTION 10 – Date of revision of text
Updated on 13 May 2018
File name
Adv_SPC_NI_8_0_UK_IE_clean.docx
Reasons for updating
- New SPC for new product
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 13 May 2018
File name
Adv HCP Leaflet NI 8_1 pfs UK IE clean.pdf
Reasons for updating
- Change to section 6 - date of revision
Updated on 04 May 2018
File name
Adv_SPC_NI_8_0_UK_IE_clean.docx
Reasons for updating
- Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
- Change to section 4.8 - Undesirable effects
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows: Section 4.5 and 4.8 update with new adolescent co-administration data (Boostrix and Cervarix).
Updated on 26 April 2018
File name
Adv_HCP_Leaflet_NI_8_0_pfs_UK_IE_clean.pdf
Reasons for updating
- Change to section 2 - interactions with other medicines, food or drink
- Change to section 6 - date of revision
Updated on 21 March 2018
Reasons for updating
- New SPC for new product
Legal category:Product subject to medical prescription which may not be renewed (A)
Updated on 21 March 2018
Reasons for updating
- Change to section 4.4 - Special warnings and precautions for use
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Updated on 09 March 2017
Reasons for updating
- Change to section 10 - Date of revision of the text
- Removal of black triangle
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows:
Black triangle is removed.
Section 10 – Date of revision is updated.Updated on 03 March 2017
Reasons for updating
- Change to section 10 - Date of revision of the text
- Removal of black triangle
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows:
Black triangle is removed.
Section 10 – Date of revision is updated.Updated on 28 February 2017
File name
PIL_15433_675.pdf
Reasons for updating
- New PIL for new product
Updated on 28 February 2017
Reasons for updating
- Removal of black triangle
Updated on 21 December 2016
Reasons for updating
- Change to section 4.1 - Therapeutic indications
- Change to section 4.2 - Posology and method of administration
- Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 5.1 - Pharmacodynamic properties
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows:
Update to section 4.1 and consequential changes to other SPC sections as follows:
4.1 Therapeutic indications
Nimenrix is indicated for active immunisation of individuals from the age of 6 weeks against invasive meningococcal diseases caused by Neisseria meningitidis group A, C, W-135, and Y.
Section 4.2 is updated to include posology for infants
Section 4,5 is updated with information on concomitant medication for infants
Section 4.8 safety profile summary is updated with information on safety in infants
Section5.1 is updated with information on immunogenicity in infants, tables and other sections have been updated accordingly.
Section 10 – Date of revision is updated.Updated on 19 December 2016
Reasons for updating
- Change to Section 1 - what the product is
- Change to section 2 - use in children and adolescents
- Change to section 2 - interactions with other medicines, food or drink
- Change to section 4 - possible side effects
- Change to section 6 - date of revision
Updated on 14 October 2016
Reasons for updating
- Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
- Change to section 5.1 - Pharmacodynamic properties
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Updates to sections 4.5 and 5.1 – please refer to track changes SPC for further details on changes/additions to the text.
Section 10 – Date of revision updated.Updated on 13 October 2016
Reasons for updating
- Change to drug interactions
- Change to date of revision
Updated on 01 September 2016
Reasons for updating
- Change to section 4.2 - Posology and method of administration
- Change to section 4.4 - Special warnings and precautions for use
- Change to section 4.8 - Undesirable effects
- Change to section 5.1 - Pharmacodynamic properties
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
The SPC has been updated as follows:
Updates to sections 4.2, 4.4, 4.8, 5.1 – please refer to track changes SPC for further details on changes/additions to the text.
Section 10 – Date of revision updated.Updated on 26 August 2016
Reasons for updating
- Change to warnings or special precautions for use
- Change to date of revision
Updated on 08 August 2016
Reasons for updating
- Change to section 4.4 - Special warnings and precautions for use
- Change to section 4.8 - Undesirable effects
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Update to SmPC section 5.1 is updated to reflect the currently observed data re the immune response following one or two doses of Nimenrix given 2 months apart was evaluated one month after the last vaccination.
Section 4.4 is updated to consider providing a second dose of Nimenrix to toddlers who are expected to have a particular risk of exposure to serogroups W-135 and Y.
Section 4.8 has been updated to reflect the safety data available from the study that a second dose of Nimenrix in toddlers, with a dose interval of 2 months, has a similar reactogenicity profile compared to the 1st dose.
Updated on 08 August 2016
Reasons for updating
- Change to date of revision
- Change to dosage and administration
Updated on 12 May 2016
Reasons for updating
- Change to section 7 - Marketing authorisation holder
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Updated on 12 May 2016
Reasons for updating
- Change to marketing authorisation holder
Updated on 09 April 2015
Reasons for updating
- Change to section 4.2 - Posology and method of administration
- Change to section 4.8 - Undesirable effects
- Change to section 5.1 - Pharmacodynamic properties
- Change to section 9 - Date of renewal of authorisation
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.2: Deletion of text
Section 4.8 Update to summary of safety profile (Update of the number of subjects included in the pooled analysis on which the safety profile is based on).
Section 5.1 - Correction of data from studies MenACWY-TT-036, -038 and -043
Updated on 19 September 2014
Reasons for updating
- Change to section 5.1 - Pharmacodynamic properties
- Change to section 6.3 - Shelf life
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Persistence of immune response – correction to the clinical data for evaluation in subjects 12 months to 55 years
Persistence of immune response in toddlers – correction to typo error ‘age’
Section 6.3
After reconstitution – correction to stability after reconstitution should be 8 hours not 48 hours.
Updated on 01 September 2014
Reasons for updating
- Change to section 5.2 - Pharmacokinetic properties
- Change to section 6.3 - Shelf life
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 5.2 – correction to footer in table 9
Section 6.3 –clarity given on reconstitution of vaccine
Updated on 29 August 2014
Reasons for updating
- Change to date of revision
- Correction of spelling/typing errors
Updated on 11 August 2014
Reasons for updating
- Change to section 4.8 - Undesirable effects
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.8 change to name of Ireland Competent Authority from IMB to HPRA.
Updated on 11 August 2014
Reasons for updating
- Change to side-effects
- Change to date of revision
- Addition of information on reporting a side effect.
Updated on 02 July 2014
Reasons for updating
- Addition of marketing authorisation holder
Updated on 06 June 2014
Reasons for updating
- Change to section 4.2 - Posology and method of administration
- Change to section 4.4 - Special warnings and precautions for use
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 5.1 - Pharmacodynamic properties
- Change to section 10 - Date of revision of the text
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.4 - Updated the warning regarding persistence of serum bactericidal antibody titres.
Section 4.8 - Updated the IMB contact details for the reporting of adverse events.
Section 5.1 - Updated the clinical data regarding persistence of immune response.
Section 10 - Updated date of revision of text.
Updated on 11 February 2014
Reasons for updating
- Change to section 4.2 - Posology and method of administration
- Change to Section 4.8 – Undesirable effects - how to report a side effect
- Change to section 5.1 - Pharmacodynamic properties
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Section 4.2 - Posology and method of administration,
Section 4.8 - Undesirable effects,
Section 5.1 - Pharmacodynamic properties
Updated on 10 February 2014
Reasons for updating
- Change to warnings or special precautions for use
Updated on 13 August 2012
Reasons for updating
- New SPC for new product
Legal category:Product subject to medical prescription which may not be renewed (A)
Free text change information supplied by the pharmaceutical company
Updated on 31 July 2012
Reasons for updating
- New PIL for new product