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Clopixol Injection 200 mg/ml

*
Pharmacy Only: Prescription

  • Company:

    Lundbeck (Ireland) Limited

  • Status:

    No Recent Update

  • Legal Category:

    Product subject to medical prescription which may not be renewed (A)

  • Active Ingredient(s):

    Zuclopenthixol Decanoate

    *Additional information is available within the SPC or upon request to the company

Updated on 01 March 2023

File name

PIL_Clopixol 200 mg-ml Sol for inj_REG_014441 v23.0.pdf

Reasons for updating

  • Change to section 4 - how to report a side effect

Updated on 01 March 2023

File name

PIL_Clopixol 200 mg-ml Sol for inj_REG_014441 v23.0.pdf

Reasons for updating

  • Change to section 4 - how to report a side effect

Updated on 01 March 2023

File name

SPC_Clopixol 200 mg-ml Sol for inj_REG_006841 v23.0.pdf

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

Legal category:Product subject to medical prescription which may not be renewed (A)

Updated on 01 March 2023

File name

PIL_Clopixol 200 mg-ml Sol for inj_REG_014441 v23.0.pdf

Reasons for updating

  • Change to section 4 - how to report a side effect

Updated on 09 April 2019

File name

PL IE Clopixol 200mg.ml_3_ clean.pdf

Reasons for updating

  • Change to section 6 - marketing authorisation holder

Updated on 09 April 2019

File name

1-3-1 IE Clopixol 200 mg per ml Portrait clean.pdf

Reasons for updating

  • New SPC for new product

Legal category:Product subject to medical prescription which may not be renewed (A)

Updated on 03 February 2017

File name

PIL_8255_805.pdf

Reasons for updating

  • New PIL for new product

Updated on 03 February 2017

Reasons for updating

  • Change to section 6 - marketing authorisation holder
  • Change to section 6 - date of revision

Updated on 30 June 2015

Reasons for updating

  • Change to date of revision
  • Change to MA holder contact details

Updated on 05 May 2015

Reasons for updating

  • Change to information about pregnancy or lactation
  • Change to date of revision
  • Change to improve clarity and readability
  • Addition of information on reporting a side effect.

Updated on 12 September 2014

Reasons for updating

  • Change to storage instructions
  • Change to date of revision

Updated on 17 May 2012

Reasons for updating

  • Change to information about pregnancy or lactation

Updated on 19 January 2012

Reasons for updating

  • Change due to user-testing of patient information

Updated on 25 August 2010

Reasons for updating

  • Change to side-effects

Updated on 12 July 2010

Reasons for updating

  • Change to warnings or special precautions for use
  • Change to side-effects

Updated on 02 December 2008

Reasons for updating

  • Correction of spelling/typing errors

Updated on 12 October 2006

Reasons for updating

  • Change to side-effects
  • Improved electronic presentation

Updated on 29 September 2006

Reasons for updating

  • Change of contraindications
  • Change to side-effects
  • Change to marketing authorisation holder

Updated on 08 June 2006

Reasons for updating

  • Improved electronic presentation

Updated on 15 September 2004

Reasons for updating

  • New PIL for medicines.ie