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Seretide 100, 250, 500 Accuhaler

Last Updated on eMC 12-Jan-2017 View document  | GlaxoSmithKline UK Contact details

When a pharmaceutical company changes an SPC or PIL, a new version is published on the eMC.  For each version, we show the dates it was published on the eMC and the reasons for change.

Updated on 12-Jan-2017 and displayed until Current

Reasons for adding or updating:

  • Change to section 4 - possible side effects
  • Change to section 6 - date of revision
  • Improved presentation of PIL

Updated on 21-Apr-2015 and displayed until 12-Jan-2017

Reasons for adding or updating:

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

Updated on 20-Apr-2015 and displayed until 21-Apr-2015

Reasons for adding or updating:

  • Change to section 4 - possible side effects
  • Change to section 6 - date of revision
  • Improved presentation of PIL

Updated on 02-Oct-2014 and displayed until 20-Apr-2015

Reasons for adding or updating:

  • Change to section 1 - what the product is used for
  • 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 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 5 - how to store
  • Change to section 6 - what the product contains
  • Change to section 6 - manufacturer
  • Change to section 6 - date of revision
  • Correction of spelling/typing errors
  • Improved presentation of PIL

Updated on 20-May-2013 and displayed until 02-Oct-2014

Reasons for adding or updating:

  • Change to section 4 - possible side effects
  • Change to section 6 - date of revision

Updated on 10-Dec-2012 and displayed until 20-May-2013

Reasons for adding or updating:

  • Change to section 4 - possible side effects
  • Change to section 6 - date of revision

Updated on 22-Dec-2011 and displayed until 10-Dec-2012

Reasons for adding or updating:

  • Change to date of revision
  • Change to side-effects

Updated on 14-Sep-2011 and displayed until 22-Dec-2011

Reasons for adding or updating:

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

Updated on 07-Dec-2009 and displayed until 14-Sep-2011

Reasons for adding or updating:

  • Change to drug interactions

Updated on 14-Jan-2009 and displayed until 07-Dec-2009

Reasons for adding or updating:

  • Extra statutory information

Updated on 02-May-2008 and displayed until 14-Jan-2009

Reasons for adding or updating:

  • Change to date of revision
  • Change due to user-testing of patient information

Updated on 24-Feb-2005 and displayed until 02-May-2008

Reasons for adding or updating:

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

Updated on 11-Mar-2004 and displayed until 24-Feb-2005

Reasons for adding or updating:

  • Change to side-effects

Updated on 31-Jul-2003 and displayed until 11-Mar-2004

Reasons for adding or updating:

  • Update to PIL

Updated on 21-Mar-2001 and displayed until 31-Jul-2003

Reasons for adding or updating:

  • No reasons supplied

Company contact details

GlaxoSmithKline UK

Company image
Address

Stockley Park West, Uxbridge, Middlesex, UB11 1BT

Fax

+44 (0)208 990 4328

Medical Information e-mail
Telephone

0800 221 441

E-mail
Customer Care direct line

0800 221 441

Before you contact this company: often several companies will market medicines with the same active ingredient. Please check that this is the correct company before contacting them. Why?

Active ingredients

fluticasone propionate, salmeterol xinafoate

Legal categories

POM - Prescription Only Medicine

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