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Adverse reactions to radiopharmaceuticals in France: analysis of the national pharmacovigilance database.
Laroche, Marie-Laure; Quelven, Isabelle; Mazère, Joachim; Merle, Louis.
Afiliação
  • Laroche ML; Service de Pharmacologie, Toxicologie et Pharmacovigilance, CHU de Limoges, Limoges, France Faculté de Médecine, Université de Limoges, Limoges, France marie-laure.laroche@chu-limoges.fr.
  • Quelven I; Service de Pharmacologie, Toxicologie et Pharmacovigilance, CHU de Limoges, Limoges, France Service de Médecine Nucléaire, CHU de Limoges, Limoges, France.
  • Mazère J; Service de Médecine Nucléaire, CHU de Bordeaux, Bordeaux, France INCIA, UMR 5287, Université de Bordeaux, Talence, France CNRS, INCIA, UMR 5287, Talence, France.
  • Merle L; Service de Pharmacologie, Toxicologie et Pharmacovigilance, CHU de Limoges, Limoges, France Faculté de Médecine, Université de Limoges, Limoges, France.
Ann Pharmacother ; 49(1): 39-47, 2015 Jan.
Article em En | MEDLINE | ID: mdl-25366341
ABSTRACT

BACKGROUND:

Radiopharmaceuticals are regarded as safe by the nuclear medicine community, but up to now, no survey has been conducted with from the perspective of pharmacovigilance.

OBJECTIVE:

To describe the adverse reactions to radiopharmaceuticals (ARRPs) reported to the French Pharmacovigilance Database (FPVD).

METHODS:

We selected and described all reports encompassing at least one radiopharmaceutical in the FPVD. The annual incidence of reported ARRPs used in diagnosis was also estimated.

RESULTS:

From 1989 to 2013, 304 reports of ARRPs were identified (43.0% serious, 12 deaths) in 54.6% women and 45.4% men; the median age was 58 years. Five therapeutic radiopharmaceuticals ((131)I-sodium iodide, (131)I-lipiodol, (89)Sr-chloride, (153)Sm-lexidronam, and (90)Y-ibritumomab-tiuxetan) were involved in 48 reports (97 adverse reactions 86.6% serious, 9 deaths). Pulmonary disorders represented 44.3% of ARRPs used for therapy, mainly related to (131)I-lipiodol. There were 34 diagnostic radiopharmaceuticals involved in 256 reports (451 adverse reactions 38.1% serious, 3 deaths); 8 diagnostic products ((99m)Tc-oxidronate, (18)F-fluorodeoxyglucose, (99m)Tc-tin pyrophosphate, (99m)Tc-tetrofosmin, (99m)Tc-dimercaptosuccinic acid, (201)Tl-chloride, (99m)Tc-sestamibi, and (111)In-pentetate) accounted for two-thirds of ARRPs. The most frequent adverse reactions were skin (34.4%), general (18.2%), nervous (9.0%), and gastrointestinal disorders (7.0%). There were 25 cases of altered images and 10 medication errors. The annual incidence of reported adverse reactions ranged from 1.2 × 10(-5) to 3.4 × 10(-5) diagnostic administrations.

CONCLUSIONS:

Reported ARRPs occurred rarely and were more serious in the therapeutic than in the diagnostic field. The notification of ARRPs was able to provide new guidance for safe use, as was the case for (131)I-lipiodol. Therefore, it is important to report ARRPs to a pharmacovigilance system.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas de Notificação de Reações Adversas a Medicamentos / Compostos Radiofarmacêuticos Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Prognostic_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas de Notificação de Reações Adversas a Medicamentos / Compostos Radiofarmacêuticos Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Prognostic_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2015 Tipo de documento: Article