WHO Pharmaceuticals Newsletter 1998, No. 09&10
(1998; 23 pages)
Table of Contents
Close this folderRegulatory decisions
View the documentAlbumin (human) B batches withdrawn: increase in aluminium level: Austria
View the documentAstemizole - warning concerning arrhythmias: Brazil
View the documentChlormezanone - withdrawn: Zimbabwe
View the documentChlorzoxazone - warning: hepatotoxicity: Chile
View the documentCidofovir - adverse reactions: nephrotoxicity, uveitis/iritis and hearing loss: Gilead Sciences, USA
View the documentFenfluramine and dexfenfluramine - temporary suspension: Brazil
View the documentFenfluramine and dexfenfluramine - warning concerning adverse reactions: Chile
View the documentIonic contrast media - notice of withdrawal: Germany
View the documentLaxatives containing aloe, bisacodyl, cascara sagrada and senna - proposed reclassification: USA
View the documentMeloxicam - data sheet revised: gastrointestinal and skin reactions: UK
View the documentMetamizole sodium - withdrawn due to agranulocytosis: Zimbabwe
View the documentMibefradil - suspended: Germany
View the documentNifedipine - re-approved in myocardial infarction: New Zealand
View the documentPsorial ointment - sales prohibited: undeclared cortisone ingredients: Sweden
View the documentPsorigon cream & lotion - withdrawn: undeclared cortisone ingredients: Germany, USA
View the documentTiclopidine - revised data sheet: thrombotic thrombocytopenic purpura: Roche, USA
View the documentTroglitazone - revised instructions for use: Parke-Davis, USA
View the documentVitamin A and betacarotene - labelling claim prohibited: USA
Open this folder and view contentsDrug surveillance
Open this folder and view contentsNew developments
Open this folder and view contentsMedical devices
Open this folder and view contentsGeneral information
Open this folder and view contentsMedication errors
Open this folder and view contentsVeterinary medicine
 

Albumin (human) B batches withdrawn: increase in aluminium level: Austria

Austria. The manufacturer of human albumin 20% and 25% (Haemoderivate: Immuno) has voluntarily recalled these products because the pharmacopoeial specification for aluminium (200 micrograms/L or less) for treatment of premature infants and dialysis patients cannot be guaranteed over the whole shelf life of 3 years when stored at temperatures above 8EC.

The increase in aluminium content over the shelf life period is due to the fact that the glass vial releases aluminium ions. This process is catalyzed by the residual citrate content of albumin preparations and depends on storage temperature as well as on the relation of inner glass surface to the amount of liquid. For 10 ml bottles, stability of the aluminium content below 200 micrograms/l cannot be guaranteed for the shelf life, irrespective of storage conditions.

In 50 ml and 100 ml bottles stored at temperatures below 8EC, the increase in aluminium content is sufficiently slowed down so that it does not rise beyond 200 micrograms/l within the 3-year shelf life. However, at storage temperatures exceeding 8EC (room temperature), the aluminium content may increase beyond 200 micrograms/l. According to available stability studies, this threshold value is not surpassed before 12 months of storage at these higher temperatures.

References: EU/EEA Rapid Alert - Defective Product Recall dated 22 September 1998, Pharmacovigilance Section, Federal Ministry of Labour, Health and Social Affairs, Vienna.

to previous section to next section
 

Last updated: May 3, 2013