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Questions and Answers Date answered: 4 March 2005

S2W-14700

To ask the Scottish Executive, further to the answer to question S2W-13712 by Mr Andy Kerr on 7 February 2005, what the remit of the medicines utilisation unit will be in addition to exploring the creation of a combined community and hospital medicines utilisation database.
Questions and Answers Date answered: 1 July 2004

S2W-09194

To ask the Scottish Executive, with reference to paragraph 4.4 of Final Consensus Statement of the Royal College of Physicians' Consensus Conference on Hepatitis C, what its response is in respect of the call for new drug therapies. The regulation and safety of medicines is reserved and is the responsibility of the Medicines and Healthcare products Regulatory Agency (MRHA), or, for certain types of drugs, the European Medicines Agency (EMEA).The MRHA has advised that any new drug applications, including those for Hepatitis C must achieve the required standards of safety, quality and efficacy before being granted a licence.
Questions and Answers Date answered: 15 November 2002

S1W-31261

They also do not include over-the-counter medicines purchased without a prescription.
Questions and Answers Date answered: 25 December 2001

S1W-20961

To ask the Scottish Executive what representations it has made to Her Majesty's Government about improving the warning of side effects on the label carried by the acne drug Isotretinoin for the benefit of GPs and patients and, if it has not, whether it will make such representations The Executive has not made any such representations and has no plans to do so.The Medicines Control Agency continuously monitors the safety of all medicines.
Official Report Meeting date: 7 June 2005

Subordinate Legislation Committee, 07 Jun 2005

Pesticides (Maximum Residue Levels in Crops, Food and Feeding Stuffs) (Scotland) Amendment (No 2) Regulations 2005 (SSI 2005/281) The regulations implement European Commission directive 2004/115/EC to substitute new residue definitions for metalaxyl and metalaxyl-M, and new maximum residue levels for a number of pesticides.
Questions and Answers Date answered: 8 November 2004

S2W-11375

In coming to a decision about the use of a medicine not specifically licensed for children, clinicians will take into account guidance from various sources including “Medicines for Children”, a UK paediatric formulary produced jointly by the Royal College of Paediatrics and Child Health and the Neonatal and Paediatri...
Questions and Answers Date answered: 12 February 2002

S1W-22464

This usually occurs when the product has been in general clinical use.HTBS also supports the Scottish Medicines Consortium, which will provide advice at the time a new medicine is marketed.Experimental treatments cannot be recommended until they are authorised by the Medicines...
Questions and Answers Date answered: 30 May 2006

S2W-25926

The regulation and safety ofmedicines are reserved and are the responsibility of the Medicines andHealthcare products Regulatory Agency (MHRA).
Questions and Answers Date answered: 27 April 2005

S2W-15742

To ask the Scottish Executive what alternatives to zometa are recommended by the Scottish Medicines Consortium (SMC) to treat skeletal-related events in prostate cancer patients.
Questions and Answers Date answered: 10 March 2005

S2W-14832

To ask the Scottish Executive how decisions of the Scottish Medicines Consortium (SMC) are monitored for implementation at NHS board level.

Can't find what you're looking for?

If you're having trouble finding the information you want, please contact [email protected].