Summary of Product Characteristics
last updated on the eMC:
20/04/2012
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 20/04/2012 and displayed until Current
|
Reasons for adding or updating:
|
-
Change to section 4.2 - Posology and method of administration
-
Change to section 10 date of revision of the text
|
| Date of revision of text on the SPC: 17-Apr-2012 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
|
| 4.2
New sections added on Recalcitrant dermatoses /Patients who frequently relapse; elderly; renal & hepatic impairment. Contraindication added for children under one year of age.
10. 17 April 2012
|
|
Updated on 10/04/2012 and displayed until 20/04/2012
|
Reasons for adding or updating:
|
-
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 4.9 - Overdose
-
Change to section 10 date of revision of the text
|
| Date of revision of text on the SPC: 30-Mar-2012 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
|
4.5 New interactions added (none previously)
4.6 Updated with new information on fertility, lactation and pregnancy
4.9 Whole section reworded
10.0 Updated with new date of revision of text
|
|
Updated on 15/02/2012 and displayed until 10/04/2012
|
Reasons for adding or updating:
|
-
Change to section 4.3 - Contraindications
-
Change to section 10 date of revision of the text
|
| Date of revision of text on the SPC: 01-Feb-2012 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
|
Section 4.3 - re-instate the “hypersensitivity” statement in this section
Section 10 - updated date of revision
|
|
Updated on 16/11/2011 and displayed until 15/02/2012
|
Reasons for adding or updating:
|
-
Change to section 5.3 - Preclinical Safety Data
-
Change to section 10 date of revision of the text
|
| Date of revision of text on the SPC: 02-Sep-2011 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
|
5.3 - Reproductive toxicity details added
Subcutaneous administration of betamethasone valerate to mice or rats at doses ≥0.1 mg/kg/day or rabbits at doses ≥12 micrograms/kg/day during pregnancy produced foetal abnormalities including cleft palate and intrauterine growth retardation.
The effect on fertility of betamethasone valerate has not been evaluated in animals.
10 - Date of information updated
|
|
Updated on 11/07/2011 and displayed until 16/11/2011
|
Reasons for adding or updating:
|
-
Change to section 5.2 - Pharmacokinetic Properties
-
Change to section 10 date of revision of the text
|
| Date of revision of text on the SPC: 07-Jul-2011 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
|
5.2. This section has been re-formatted with no additional new information.
10. Amended with approval date.
|
|
Updated on 06/07/2011 and displayed until 11/07/2011
|
Reasons for adding or updating:
|
-
Change to section 4.7 - Effects on Ability to Drive and Use Machines
-
Change to section 10 date of revision of the text
|
| Date of revision of text on the SPC: 01-Jul-2011 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
|
4.7 - Section 4.7 of SmPC: updated in line with SmPC guideline for this section.
10.0 - Date of revision
|
|
Updated on 17/10/2007 and displayed until 06/07/2011
|
Reasons for adding or updating:
|
-
Change to section 4.1 - Therapeutic indications
-
Change to section 5.1 - Pharmacodynamic Properties
-
Change to section 7 - Marketing Authorisation Holder
-
Change to section 9 - Date of first Authorisation/renewal of the Authorisation
-
Change to section 10 date of revision of the text
|
| Date of revision of text on the SPC: 09/2007 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
|
|
4.1 Therapeutic Indications
Typographical error corrected.
7. Marketing Authorisation Holder
Alternative registered trading style re-instated.
9. Date of First Authorisation/Renewal of Authorisation
Updated to reflect the renewal date and current SPC guidance.
10. Date of the Revision of Text
Updated to reflect the renewal date.
|
|
Updated on 18/02/2005 and displayed until 17/10/2007
|
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 4.9 - Overdose
|
|
Updated on 10/03/2003 and displayed until 18/02/2005
|
Reasons for adding or updating:
|
-
Change to section 7 - Marketing Authorisation Holder
|
|
Updated on 08/05/2002 and displayed until 10/03/2003
|
Reasons for adding or updating:
|
-
Improved Electronic Presentation
|
|
Updated on 14/08/2001 and displayed until 08/05/2002
|
Reasons for adding or updating:
|
-
Transferred from eMC version 1
|
|
Updated on 07/06/2000 and displayed until 14/08/2001
|
Reasons for adding or updating:
|
|
|
|
Updated on 06/09/1999 and displayed until 07/06/2000
|
Reasons for adding or updating:
|
|
|
|