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GlaxoSmithKline UK
Stockley Park West, Uxbridge, Middlesex, UB11 1BT
Telephone: +44 (0)800 221 441
Fax: +44 (0)208 990 4328
Medical Information e-mail: customercontactuk@gsk.com

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?
Summary of Product Characteristics last updated on the eMC: 07/06/2010
SPC Augmentin 125/31 SF Suspension

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 07/06/2010 and displayed until Current
Reasons for adding or updating:
  • Change to section 2 - Qualitative and quantitative composition
  • Change to section 3 - Pharmaceutical form
  • Change to section 4.1 - Therapeutic indications
  • Change to section 4.2 - Posology and method of administration
  • Change to section 4.3 - Contraindications
  • 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 4.6 - Pregnancy and Lactation
  • Change to section 4.7 - Effects on Ability to Drive and Use Machines
  • Change to section 4.8 - Undesirable Effects
  • Change to section 4.9 - Overdose
  • Change to section 5.1 - Pharmacodynamic Properties
  • Change to section 5.2 - Pharmacokinetic Properties
  • Change to section 5.3 - Preclinical Safety Data
  • Change to section 6. 5 - Nature and Contents of Container
  • Change to section 6. 6 - Instructions for use, handling and disposal
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   01-Jun-2010
Legal Category:   POM
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company
Section 2 - Changes to nearly all sections following an Article 30 Procedure

Section 3 - Changes to nearly all sections following an Article 30 Procedure

Section 4.1 - Changes to nearly all sections following an Article 30 Procedure

Section 4.2 - Changes to nearly all sections following an Article 30 Procedure

Section 4.3 - Changes to nearly all sections following an Article 30 Procedure

Section 4.4 - Changes to nearly all sections following an Article 30 Procedure

Section 4.5 - Changes to nearly all sections following an Article 30 Procedure

Section 4.6 - Changes to nearly all sections following an Article 30 Procedure

Section 4.7 - Changes to nearly all sections following an Article 30 Procedure

Section 4.8 - Changes to nearly all sections following an Article 30 Procedure

Section 4.9 - Changes to nearly all sections following an Article 30 Procedure

Section 5.1 - Changes to nearly all sections following an Article 30 Procedure

Section 5.2 - Changes to nearly all sections following an Article 30 Procedure

Section 6.5 - Changes to nearly all sections following an Article 30 Procedure

Section 6.6 - Changes to nearly all sections following an Article 30 Procedure

Section 10 - Changes to nearly all sections following an Article 30 Procedure
Updated on 28/08/2007 and displayed until 07/06/2010
Reasons for adding or updating:
  • Change to section 6. 3 - Shelf Life
  • Change to section 10 date of revision of the text
Date of revision of text on the SPC:   08/2007
Legal Category:   POM
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company
Section 6.3 Shelf-life
 
Augmentin 125/31 SF Suspension Dry powder: 18M 24 months                                                                       
                                                            Reconstituted suspensions: 7 days"


Section 10: To change the date from "3 April 2006" to "15 August 2007"
Updated on 24/11/2006 and displayed until 28/08/2007
Reasons for adding or updating:
  • Addition of separate SPCs covering individual presentations
Date of revision of text on the SPC:   04/2006
Legal Category:   POM
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company

For further information, please contact GlaxoSmithKline on +44 (0)800 221 441

Active Ingredients/Generics

 
  co-amoxiclav