Summary of Product Characteristics
last updated on the eMC:
04/02/2009
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 04/02/2009 and displayed until Current
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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 6.1 - List of Excipients
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Change to section 6. 4 - Special Precautions for Storage
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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: 30-Jan-2009 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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3. PHARMACEUTICAL form
pH information added:
The pH of reconstituted solution is 7.0 – 8.2.
6.1 List of excipients
Mannitol
Sodium hydroxide or Hydrochloric acid pH wording added:(for pH adjustment)
6.4 Special precautions for storage
Wording changed to:Store in a refrigerator (2°C – 8°C)
10. DATE OF REVISION OF THE TEXT
30th January 2009
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Updated on 14/01/2009 and displayed until 04/02/2009
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Reasons for adding or updating:
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Change to section 4.2 - Posology and method of administration
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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 5.2 - Pharmacokinetic Properties
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| Date of revision of text on the SPC: 03-Nov-2008 |
| Legal Category: POM |
| Black Triangle (CHM):
NO |
Free-text change information supplied by the pharmaceutical company
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- Update to section 4.2 and 5.2 with regards to creatinine clearance levels for treatment with pentostatin in patients with impaired renal function.
- To bring the SPC in line with the current QRD format.
- wording of Section 4.7 (Effects of ability to drive and use machines) has been updated for clarity
- section 4.8 has been updated following full review of the safety database.
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Updated on 11/02/2008 and displayed until 14/01/2009
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Reasons for adding or updating:
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