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Questions and Answers Date answered: 6 January 2000

S1W-03564

Details of each Health Board's allocations are as follows: Col. 1Col 2Col 3 TotalUnifiedBudgetPercentageIncrease inUnifiedBudgetNon-CashLimitedFamilyHealthServicesHealth Board£mm Argyll & Clyde358.8205.4251.449Ayrshire & Arran306.0205.2543.080Borders88.7515.3212.605Dumfries & Galloway 128.7385.2317.2...
Questions and Answers Date answered: 12 October 1999

S1W-01322

Progress thereafter will depend on public reaction to the proposals and the availability of funding.LocationDescriptionLength (m)Estimated Cost (£m)CrossroadsNew wide single carriageway south of Crossroads with roundabout at junction11300.900GatesideNew single carriageway off line north of Gateside Farm to provide im...
Questions and Answers Date answered: 27 July 2004

S2W-09472

Information for patients onhow to use medicines safely and effectively is provided in the PatientInformation Leaflet , which accompanies the medicine.
Questions and Answers Date answered: 11 December 2003

S2W-04452

Information on side-effectssuspected to be associated with vaccines or medicinal products is routinelycollected in the UK by the Committee on Safety of Medicines (CSM) andMedicines and Healthcare products Regulatory Agency (MHRA).
Questions and Answers Date answered: 19 August 2003

S2W-01362

To ask the Scottish Executive how many products have been removed from the approved list of medicines by the Scottish Medicines Consortium since its establishment.
Questions and Answers Date answered: 1 August 2003

S2W-01361

The Medicines and Healthcare products Regulatory Agency (MHRA) (the former Medicines Control Agency) licenses products on the basis of safety, quality and efficacy.
Official Report Meeting date: 28 September 2006

Plenary, 28 Sep 2006

Can he assure me that the treatment will be readily available to those patients for whom it is deemed to be clinically appropriate? The point that medicines should be used where they are clinically appropriate is important.
Questions and Answers Date answered: 20 September 2006

S2W-28186

Before a medicine can be placed on the UK market it must have a marketingauthorisation either from the MHRA or the European Medicines Agency (EMEA).
Questions and Answers Date answered: 24 April 2006

S2W-24896

To ask the Scottish Executive what measures are in place to ensure that funds allocated for expenditure on medicines are used for this purpose. No specific allocation ismade to NHS boards for expenditure on medicines.
Questions and Answers Date answered: 21 March 2002

S1W-23886

The Scottish Executive has had no discussions with the Medicines Control Agency regarding any non-compliance in the NHS with the requirements of the Medicines for Human Use (Marketing Authorisations, etc.)

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