| Modification | Date |
| Change to section 4.4 - Special warnings and precautions for Use | 02/11/2009 10:09:38 |
| Change to section 6. 5 - Nature and Contents of Container | 02/11/2009 10:09:38 |
| Change to section 6. 4 - Special Precautions for Storage | 02/11/2009 10:09:38 |
| Change to section 6. 3 - Shelf Life | 02/11/2009 10:09:38 |
| Change to section 4.8 - Undesirable Effects | 23/07/2009 09:34:27 |
| Change to section 4.5 - Interaction with other medicinal products and other forms of interaction | 23/07/2009 09:34:27 |
| Change to section 4.3 - Contraindications | 23/07/2009 09:34:27 |
| Change to section 10 date of revision of the text | 01/09/2008 09:54:11 |
| Change to section 7 - Marketing Authorisation Holder | 01/09/2008 09:54:11 |
| Change to section 10 date of revision of the text | 24/06/2008 10:16:21 |
| Change to section 9 - Date of first Authorisation/renewal of the Authorisation | 24/06/2008 10:16:21 |
| Change to separate SPCs covering individual presentations | 10/06/2008 10:16:06 |
| Change to section 4.4 - Special warnings and precautions for Use | 01/05/2007 16:33:13 |
| Change from BAN to rINN | 01/05/2007 15:51:44 |
| Change to section 10 (date of (partial) revision of the text | 01/05/2007 15:51:44 |
| Change to section 6. 3 - Shelf Life | 01/05/2007 15:51:44 |
| Change to section 4.4 - Special Warnings and Precautions for Use | 01/05/2007 15:51:44 |
| Change to section 4.3 - Contra-indications | 01/05/2007 15:51:44 |
| Change to section 6.1 - List of Excipients | 12/08/2005 15:29:19 |
| Addition of joint SPC covering all presentations | 01/09/2003 14:27:17 |
| Change to section 7 - Marketing Authorisation Holder | 01/09/2003 14:27:17 |
| New SPC for new product | 01/09/2003 14:27:17 |
|