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
Summary of Product Characteristics last updated on the eMC: 30/03/2009
SPC Ambirix suspension for injection

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 30/03/2009 and displayed until Current
Reasons for adding or 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
  • Change to section 6.1 - List of Excipients
Date of revision of text on the SPC:   05-Sep-2007
Legal Category:   POM
Black Triangle (CHM):   YES

Free-text change information supplied by the pharmaceutical company

Section 4.4 - Deleted "Thiomersal (an organomercuric compound) has been used in the manufacturing process of this medicinal product and residues of it are present in the final product. Therefore, sensitisation reactions may occur."

Section 4.8 - Added "The current formulation of Ambirix does not contain thiomersal (an organomercuric compound) or any preservative. In a clinical study conducted with 3 doses of the current formulation in adults, the incidence of pain, redness, swelling, fatigue, gastro-enteritis, headache and fever was comparable to the incidence observed with the former thiomersal and preservative containing vaccine formulation. The following adverse reactions have been reported following the widespread use of the former formulation"

Section 5.1 - Added "These data were generated with the former Ambirix formulation containing thiomersal and a preservative. A clinical study conducted with 3 doses of the current formulation in adults showed that the current formulation elicited similar seroprotection and seroconversion rates as compared to the former formulation.

Section 6.1 - Deleted "phenoxyethanol"
Updated on 17/02/2009 and displayed until 30/03/2009
Reasons for adding or 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
  • Change to section 6.1 - List of Excipients
Date of revision of text on the SPC:   05-Sep-2007
Legal Category:   POM
Black Triangle (CHM):   YES

Free-text change information supplied by the pharmaceutical company

Section 4.4 - Reintroduced "Thiomersal (an organomercuric compound) has been used in the manufacturing process of this medicinal product and residues of it are present in the final product. Therefore, sensitisation reactions may occur."

Section 4.8 - Deleted "The current formulation of Ambirix does not contain thiomersal (an organomercuric compound) or any preservative. In a clinical study conducted with 3 doses of the current formulation in adults, the incidence of pain, redness, swelling, fatigue, gastro-enteritis, headache and fever was comparable to the incidence observed with the former thiomersal and preservative containing vaccine formulation. The following adverse reactions have been reported following the widespread use of the former formulation"

Section 5.1 - Deleted "These data were generated with the former Ambirix formulation containing thiomersal and a preservative. A clinical study conducted with 3 doses of the current formulation in adults showed that the current formulation elicited similar seroprotection and seroconversion rates as compared to the former formulation."

Section 6.1 - Reintroduced "phenoxyethanol"
Updated on 03/02/2009 and displayed until 17/02/2009
Reasons for adding or 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
  • Change to section 6.1 - List of Excipients
Date of revision of text on the SPC:   05-Sep-2007
Legal Category:   POM
Black Triangle (CHM):   YES

Free-text change information supplied by the pharmaceutical company

Section 4.4 - Deleted "Thiomersal (an organomercuric compound) has been used in the manufacturing process of this medicinal product and residues of it are present in the final product. Therefore, sensitisation reactions may occur."

Section 4.8 - Added "The current formulation of Ambirix does not contain thiomersal (an organomercuric compound) or any preservative. In a clinical study conducted with 3 doses of the current formulation in adults, the incidence of pain, redness, swelling, fatigue, gastro-enteritis, headache and fever was comparable to the incidence observed with the former thiomersal and preservative containing vaccine formulation. The following adverse reactions have been reported following the widespread use of the former formulation"

Section 5.1 - Added "These data were generated with the former Ambirix formulation containing thiomersal and a preservative. A clinical study conducted with 3 doses of the current formulation in adults showed that the current formulation elicited similar seroprotection and seroconversion rates as compared to the former formulation."

Section 6.1 - Deleted "phenoxyethanol"
Updated on 08/01/2008 and displayed until 03/02/2009
Reasons for adding or updating:
  • New SPC for new product


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