Summary of Product Characteristics
last updated on the eMC:
20/11/2009
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 20/11/2009 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 8 - MARKETING AUTHORISATION NUMBER(S)
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Change to section 9 - Date of first Authorisation/renewal of the Authorisation
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| Date of revision of text on the SPC: 03-Nov-2009 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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Minor change to the expression of the product name as follows:
From 'Sinemet CR 50/200 mg Prolonged-Release Tablets' to 'Sinemet CR 50 mg/200 mg Prolonged-Release Tablets'
From 'Half Sinemet CR 25/100 mg Prolonged-Release Tablets' to 'Half Sinemet CR 25 mg/100 mg Prolonged-Release Tablets'
Fromto
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Updated on 31/07/2009 and displayed until 20/11/2009
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Reasons for adding or updating:
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Change to section 7 - Marketing Authorisation Holder
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Product Acquisition
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| Date of revision of text on the SPC: 30-Apr-2009 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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| The marketing of the Sinemet range has been transferred to Merck Sharp & Dohme Limited as of 1 August 2009 from BMS. Section 7 of the SPC has been updated to remove BMS as a licenced distributor.
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Updated on 14/01/2009 and displayed until 31/07/2009
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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 6. 4 - Special Precautions for Storage
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Change to section 8 - MARKETING AUTHORISATION NUMBER(S)
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Change to section 9 - Date of first Authorisation/renewal of the Authorisation
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| Date of revision of text on the SPC: 31-Oct-2008 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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Section 1: Product names changed to include strength and pharmaceutical form
Section 6.4: The wording of the storage statement has been harmonised across the product range
Section 8: Product names changed to include strength and pharmaceutical form
Section 9: Product names changed to include strength and pharmaceutical form and section updated to reflect last renewal date
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Updated on 07/05/2008 and displayed until 14/01/2009
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Reasons for adding or updating:
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Change to section 4.4 - Special warnings and precautions for Use
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| Date of revision of text on the SPC: 21-Apr-2008 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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| To update section 4.4 of the SPC to include information relating to Melanoma; consequentially the PIL has been updated
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Updated on 13/04/2007 and displayed until 07/05/2008
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Reasons for adding or updating:
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Change to section 4.4 - Special warnings and precautions for Use
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Change to section 4.8 - Undesirable Effects
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Change to section 7 - Marketing Authorisation Holder
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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: 04/2007 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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4.4 Special warnings and precautions for use
Addition of:
Pathological gambling, increased libido and hypersexuality have been reported in patients treated with dopamine agonists for Parkinson's disease
4.8 Undesirable effects
Addition of:
Patients treated with dopamine agonists for treatment of Parkinson's disease, especially at high doses, have been reported as exhibiting signs of pathological gambling, increased libido and hypersexuality, generally reversible upon reduction of dose or treatment discontinuation.
7. MARKETING AUTHORISATION HOLDER
Distributed by
Updated to:
Bristol-Myers Squibb Pharmaceuticals Limited,
Sanderson Road, Uxbridge UB8 1DH, UK
10. DATE OF REVISION OF THE TEXT
Updated to:
April 2007
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Updated on 19/01/2005 and displayed until 13/04/2007
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Reasons for adding or updating:
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Change to section 3 - pharmaceutical form
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Change to section 10 (date of (partial) revision of the text
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Updated on 23/10/2003 and displayed until 19/01/2005
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Reasons for adding or updating:
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Change to section 4.5 - Interactions with other Medicaments and other forms of Interaction
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Updated on 13/05/2003 and displayed until 23/10/2003
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Reasons for adding or updating:
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Correction of spelling/typing errors
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Updated on 07/02/2003 and displayed until 13/05/2003
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Reasons for adding or updating:
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Change to section 4.4 - Special Warnings and Precautions for Use
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Change to section 4.7 - Effects on Ability to Drive and Use Machines
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Change to section 4.8 - Undesirable Effects
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Change to section 10 (date of (partial) revision of the text
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Updated on 23/07/2002 and displayed until 07/02/2003
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Reasons for adding or updating:
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New SPC for eMC ie an SPC for an existing product, but one that is new for the eMC
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