Summary of Product Characteristics
last updated on the eMC:
11/05/2010
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 11/05/2010 and displayed until Current
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Reasons for adding or updating:
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Change to section 1 -Name of the Medicinal product
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Change to section 2 - Qualitative and quantitative composition
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Change to section 4.8 - Undesirable Effects
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Change to section 4.9 - Overdose
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Change to section 6. 6 - Instructions for use, handling and disposal
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Change to section 9 - Date of first Authorisation/renewal of the Authorisation
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Change to section 10 date of revision of the text
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| Date of revision of text on the SPC: 23-Sep-2009 |
| Legal Category: P |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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| The following sections have been updated:
- 1. Product name: add ‘1200 mg/800 I.U.’ to the product name
- 2. Composition: add details of excipients - also contains 2 mg sunset yellow FCF (E110) and not more than 8.8 mg sucrose per dose.
- 4.8. Side-effects: Section rewritten and undesirable effects listed according to MedRA System Organ Class.
- 4.9. Overdose: More detailed information added
- 6.6. Instructions for use: Add details of appearance of the product once reconstituted (smooth orange opaque suspension with visible white granules)
- 9. Date of renewal: Renewal date added.
- 10. Date of revision of the test: Date updated.
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Updated on 25/09/2008 and displayed until 11/05/2010
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Reasons for adding or updating:
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Change to section 6. 5 - Nature and Contents of Container
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Change to section 10 date of revision of the text
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| Date of revision of text on the SPC: 01-May-2008 |
| Legal Category: P |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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| Section 6.5 Add a new pack size - 2 sachets
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Updated on 18/01/2007 and displayed until 25/09/2008
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Reasons for adding or updating:
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