Summary of Product Characteristics
last updated on the eMC:
04/05/2010
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 04/05/2010 and displayed until Current
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Reasons for adding or updating:
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Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
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Change to section 4.8 - Undesirable Effects
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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: 12-Apr-2010 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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Section 4.5
New additional text 3rd paragraph:
Concomitant use of baclofen may increase the antihypertensive effect making dose adjustments necessary.
Section 4.8
Additional undesirable effect in section of Gastrointestinal disorders:
Not known: Constipation.
Section 10
Date of revision of text: 12 April 2010
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Updated on 18/02/2010 and displayed until 04/05/2010
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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 10 date of revision of the text
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| Date of revision of text on the SPC: 08-Feb-2010 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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Section 1
Change of name to :
Tenoretic 100 mg/25 mg film coated tablets
(Also changed throughout document)
Section 10
Change of date to :
8th February 2010
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Updated on 17/12/2008 and displayed until 18/02/2010
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Reasons for adding or updating:
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Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
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Change to section 4.8 - Undesirable Effects
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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: 28-Apr-2008 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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Section 4.5
Text in 5th paragraph - include information on the potential additive pharmacodynamic effects of atenolol and amiodarone
Section 4.8
The frequency descriptors for the current adverse drug reactions have been added to section 4.8 and the system organ classes have been updated according to MedDRA terminology.
Section 10
Date of revision of text: 28 April 2008
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Updated on 10/03/2005 and displayed until 17/12/2008
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Reasons for adding or updating:
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Change to section 2 - qualitative and quantitative composition
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Change to section 3 - pharmaceutical form
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Change to section 4.2 - Posology and Method of Administration
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Change to section 4.3 - Contra-indications
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Change to section 4.4 - Special Warnings and Precautions for Use
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Change to section 4.6 - Pregnancy and Lactation
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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 5 - Pharmacological Properties
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Change to section 5.1 - Pharmacodynamic Properties
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Change to section 5.2 - Pharmacokinetic Properties
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Change to section 5.3 - Preclinical Safety Data
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Change to section 6.1 - List of Excipients
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Change to section 6.2 - Incompatibilities
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Change to section 6. 4 - Special Precautions for Storage
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Change to section 6. 5 - Nature and Contents of Container
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Change to section 6. 6 - Instruction for Use/Handling
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Change to section 9 - Date of Renewal of Authorisation
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Change to section 10 (date of (partial) revision of the text
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Updated on 14/01/2002 and displayed until 10/03/2005
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Reasons for adding or updating:
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Change to section 7 - Marketing Authorisation Holder
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Updated on 05/12/2001 and displayed until 14/01/2002
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Reasons for adding or updating:
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Change to section 7 - Marketing Authorisation Holder
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Updated on 21/08/2001 and displayed until 05/12/2001
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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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Updated on 02/07/2001 and displayed until 21/08/2001
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Reasons for adding or updating:
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Updated on 16/10/2000 and displayed until 02/07/2001
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Updated on 06/09/1999 and displayed until 16/10/2000
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