WHO Pharmaceuticals Newsletter 2002, No. 01
(2002; 18 pages) View the PDF document
Table of Contents
View the documentEDITORIAL
Open this folder and view contentsREGULATORY MATTERS
Close this folderSAFETY OF MEDICINES
View the documentBLOOD PRODUCT INFUSIONS - Risk of fatal acute lung injury (USA)
View the documentCLOZAPINE, OLANZEPINE, QUETIAPINE, RISPERIDONE - Atypical antipsychotics and glucose metabolism disorders (Canada)
View the documentDESOGESTREL/ GESTODENE ORAL CONTRACEPTIVES - Low risk of venous thromboembolism (Europe)
View the documentDIGOXIN - Increased toxicity following P-glycoprotein inhibition (Australia)
View the documentDTaP VACCINE BOOSTERS - Extensive limb swelling (Australia)
View the documentEPOETIN ALFA - Reports of pure red blood cell aplasia (Canada, U.K.)
View the documentGLITAZONES - Important safety reminder (Canada, UK)
View the documentINHALED CORTICO-STEROIDS - Use lowest effective dose in children (New Zealand)
View the documentISONIAZID, PYRAZINAMIDE, RIFAMPICIN - Reports of liver disorders (Canada)
View the documentLAMOTRIGINE - Dispensing errors due to name confusion (USA)
View the documentLINEZOLID - Reports of haematological disorders (UK)
View the documentMMR vaccine - Serology tests before giving second dose if ITP occurs (UK)
View the documentNITROFURANTOIN - Peripheral neuropathy (Australia)
View the documentNONACOG ALFA - Further studies for additional data (Europe)
View the documentOPRELVEKIN - Papilloedema in paediatric patient study (USA)
View the documentRALOXIFENE - Reports of thromboembolic events (Australia)
View the documentTIAPROFENIC ACID - Reports of cystitis (New Zealand)
View the documentTRADITIONAL MEDICINES - Adulterants/ undeclared ingredients pose safety concerns (New Zealand, UK)
View the documentTRAMADOL - Precipitation of serotonin syndrome (Australia)
Open this folder and view contentsDRUGS OF CURRENT INTEREST
Open this folder and view contentsFEATURE
 

MMR vaccine - Serology tests before giving second dose if ITP occurs (UK)

The UK CSM has recommended that patients who develop idiopathic thrombo-cytopenic purpura (ITP) within 6 weeks of receiving their first dose of measles, mumps and rubella (MMR) vaccine undergo a serological evaluation prior to receiving a second dose. The second dose is recommended where the patient is not fully immune against measles, mumps and rubella infections. These recommendations, which have been published on the website of the UK MCA, were made after the CSM reviewed all the available evidence on MMR vaccine and ITP. Particular attention was given to the risk/benefit balance associated with giving a second dose of MMR vaccine to patients who developed ITP within 6 weeks of their first dose of the vaccine. The MCA reports that, according to a recently published study, the absolute risk of developing ITP after receipt of a first MMR vaccination is 1/22 300 cases (with 2/3 ITP cases attributable to MMR vaccine); this is lower than the risk of developing ITP with wild measles (common) or rubella infections (1/3000 cases). The report also points out that the MMR vaccine product information is currently being revised to reflect the recommendations of the CSM.

Reports in WHO file: purpura thrombocytopenic 133

Reference:

Current Problems in Pharmacovigilance 27: 15, Aug 2001.

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Last updated: May 3, 2013