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The clinical and cost-effectiveness of Pharmalgen? for the treatment of bee and wasp venom allergy
1 TITLE OF PROJECT
The clinical and cost effectiveness of Pharmalgen? for the treatment of bee and wasp venom allergy
2 TAR TEAM
Liverpool Reviews and Implementation Group LRiG, University of Liverpool
Correspondence to:
Rumona Dickson, Ms
Director, LRiG
University of Liverpool
Room 2.12
Whelan Building
The Quadrangle
Brownlow Hill
Liverpool
L69 3GB
Tel: +44 0 151 794 5682
Fax: +44 0151 794 5585
Email: R.Dickson@
For details of expertise within the TAR team, see section 73 PLAIN ENGLISH SUMMARY
Allergic reactions to bee and wasp venom may occur in venom-sensitive patients immediately following a sting, and can vary in severity, with initially mild symptoms sometimes progressing to critical conditions within seconds. The most severe systemic allergic reactions generalised reactions are known as anaphylaxis, a reaction characterised by abnormally low blood pressure, fainting or collapse, and in extreme reactions these symptoms can cause deathEach year in the UK there are between two and nine deaths from anaphylaxis caused by bee and wasp venom. The immediate treatment for severe allergic reactions to bee and wasp venom consists of emergency treatment with drugs to decrease the patient’s response to the venom and support breathing, if requiredTo avoid further reactions, the use of sensitisation to bee and wasp venom, through a process known as venom immunotherapy VIT, has been investigated. Venom immunotherapy consists of subcutaneous injections of increasing amounts of venom into patients with a history of anaphylaxis to bee and wasp venom. Pharmalgen? has had UK marketing authorisation for the diagnosis and treatment using VIT of allergy to bee venom using Pharmalgen? Bee Venom and wasp venom using Pharmalgen? Wasp Venom since March 1995, and it is used by more than 40 centres across the UK. This review aims to assess whether using Pharmalgen? in VIT
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