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Imuran Powder for Solution for Injection or Infusion 50mg

  • Name:

    Imuran Powder for Solution for Injection or Infusion 50mg

  • Company:
    info
  • Active Ingredients:

    azathioprine sodium

  • Legal Category:

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

Patient Information Leaflet Patient Information Leaflet last updated on medicines.ie: 24/12/19

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Summary of Product Characteristics last updated on medicines.ie: 24/12/2019

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When a pharmaceutical company changes any document, a new version is published on medicines.ie. For each version, we show the dates it was published on medicines.ie and the reasons for change.

Updated on 24 December 2019

Reasons for updating

  • Change to section 4.4 - Special warnings and precautions for use
  • Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
  • Change to section 10 - Date of revision of the text

Updated on 24 December 2019 PIL

Reasons for updating

  • Change to section 2 - interactions with other medicines, food or drink
  • Change to section 6 - date of revision

Updated on 6 December 2019

Reasons for updating

  • Change to section 4.4 - Special warnings and precautions for use
  • Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
  • Change to section 4.8 - Undesirable effects
  • Change to section 10 - Date of revision of the text

Updated on 18 December 2018 PIL

Reasons for updating

  • Change to Section 1 - what the product is
  • Change to section 1 - what the product is used for
  • Change to section 2 - what you need to know - contraindications
  • Change to section 2 - what you need to know - warnings and precautions
  • Change to section 2 - interactions with other medicines, food or drink
  • Change to section 2 - pregnancy, breast feeding and fertility
  • Change to section 2 - excipient warnings
  • Change to section 3 - use in children/adolescents
  • Change to section 3 - how to take/use
  • Change to section 3 - overdose, missed or forgotten doses
  • Change to section 4 - possible side effects
  • Change to section 4 - how to report a side effect
  • Change to section 6 - date of revision
  • Improved presentation of PIL

Updated on 18 December 2018

Reasons for updating

  • New SmPC for new product

Updated on 11 October 2017 PIL

Reasons for updating

  • New PIL for new product

Updated on 11 October 2017 PIL

Reasons for updating

  • Change to section 6 - date of revision
  • Change to section 2 - what you need to know - warnings and precautions

Updated on 3 May 2017 PIL

Reasons for updating

  • Change to section 2 - what you need to know - warnings and precautions
  • Change to section 4 - how to report a side effect
  • Change to section 6 - marketing authorisation holder
  • Change to section 6 - date of revision

Updated on 10 January 2017 PIL

Reasons for updating

  • Change to section 2 - what you need to know - warnings and precautions
  • Change to section 6 - date of revision

Updated on 7 April 2014 PIL

Reasons for updating

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

Updated on 6 March 2013 PIL

Reasons for updating

  • Change to improve clarity and readability
  • Change due to user-testing of patient information

Updated on 24 October 2012 PIL

Reasons for updating

  • Correction of spelling/typing errors

Updated on 1 June 2011 PIL

Reasons for updating

  • Change to MA holder contact details

Updated on 3 May 2011 PIL

Reasons for updating

  • Change to marketing authorisation holder

Updated on 12 March 2010 PIL

Reasons for updating

  • Change to marketing authorisation holder

Updated on 31 January 2007 PIL

Reasons for updating

  • Change to side-effects

Updated on 4 August 2005 PIL

Reasons for updating

  • Improved electronic presentation

Updated on 25 May 2005 PIL

Reasons for updating

  • New PIL for medicines.ie