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Drug-associated anaphylaxis: 20 years of reporting in the Netherlands (1974–1994) and review of the literature

✍ Scribed by M. M. VAN DER KLAUW; J. H. P. WILSON; B. H. CH. STRICKER


Book ID
108686873
Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
713 KB
Volume
26
Category
Article
ISSN
0954-7894

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✦ Synopsis


Summary

Background
Since 1963, the Drug Safety Unit of the Dutch Inspectorate for Health Care (DSU) holds a voluntary reporting system.

Objective
To analyse all reports received in the years 1974 to 1994, registered as anaphylaxis or as a diagnosis that could contain cases of anaphylaxis.

Methods
All reports were classified as probable or possible anaphylaxis according to previously described criteria and the causal relationship between exposure and anaphylaxis was assessed.

Results
Nine hundred and ninety‐two reports possibly concerning anaphylaxis were received between 1974 and 1994. Fifty‐six were unclassifiable. The remaining 936 reports concerned 326 men and 610 women. Three hundred and forty‐five reports were classified as anaphylaxis probable, 485 as anaphylaxis possible, and 106 as anaphylaxis unlikely by previously specified criteria. Drugs frequently associated with anaphylaxis (causal relationship certain or probable) were: glafenine (326 reports classified as anaphylaxis probable or possible), combination preparations with (propy)phenazone or propyphenazone/phenacetine (39), diclofenac (30), dextran (20), ibuprofen (14), floctafenine (12), allergen extracts (12), sulfamethoxazole with trimethoprim (12), and trimethoprim (11). There is probably substantial under‐reporting as well as reporting bias in these data. Furthermore, many reports were classified as possible and not as probable anaphylaxis because the temporal relationship was unknown or not reported.

Conclusion
Drugs that caused anaphylaxis most frequently were glafenine, NSAID and certain antibiotics. Data from a voluntary reporting system such as the DSU are valuable as an early warning system for drugs that may induce anaphylactic reactions.


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In this descriptive study, all 425 reports were included concerning drug-associated agranulocytosis as registered between 1974 and 1994 in the files of the Drug Safety Unit of the Dutch Inspectorate for Health Care. All reports were analysed as to the probability of agranulocytosis or neutropenia ac