Sr. Hesslewood et Dh. Keeling, FREQUENCY OF ADVERSE REACTIONS TO RADIOPHARMACEUTICALS IN EUROPE, European journal of nuclear medicine, 24(9), 1997, pp. 1179-1182
A prospective survey was performed in 17 nuclear medicine departments
during 1996 in an attempt to provide reliable data on the prevalence o
f adverse reactions to radiopharmaceuticals. All adverse events follow
ing radiopharmaceutical administration were recorded, irrespective of
the severity or likelihood of causality, and subsequently analysed usi
ng an algorithm developed by Silberstein et al., designed to establish
a cause-effect relationship. A prevalence of 11 events per 10(5) admi
nistrations was obtained (95% confidence limits 3.3-19.2). No serious
of life-threatening events were reported. This rate is slightly higher
than that obtained in a larger scale study in the United States (2.3
events per 10(5) administrations, 95% confidence limits 1.2-3.4). The
difference may be due to the decision to include or exclude vasovagal
events from the analysis, the way in which the algorithm was used and
the comparative size and time scale of the two studies. The prevalence
of adverse reactions is approximately 1000-fold than less that occurr
ing with iodinated contrast media and drugs.