Abstract
Purpose/Background A recent article in this journal presented a US perspective regarding the modernization of clozapine prescription and proposed an escape from the long shadow cast by agranulocytosis. Methods Here, an international group of collaborators discusses a point of view complementary to the US view by focusing on worldwide outcomes of clozapine usage that may be uneven in terms of frequency of clozapine adverse drug reactions. Findings/Results Studies from the Scandinavian national registries (Finland and Denmark) did not find increased mortality in clozapine patients or any clear evidence of the alleged toxicity of clozapine. Data on clozapine-associated fatal outcomes were obtained from 2 recently published pharmacovigilance studies and from the UK pharmacovigilance database. A pharmacovigilance study focused on physician reports to assess worldwide lethality of drugs from 2010 to 2019 found 968 clozapine-associated fatal outcomes in the United Kingdom. Moreover, the United Kingdom accounted for 55% (968 of 1761) of worldwide and 90% (968 of 1073) of European fatal clozapine-associated outcomes. In a pharmacovigilance study from the UK database (from 2008 to 2017), clozapine was associated with 383 fatal outcomes/year including all reports from physicians and nonphysicians. From 2018 to 2021, UK clozapine-associated fatal outcomes increased to 440/year. Implications/Conclusions The interpretation of fatal outcomes in each country using pharmacovigilance databases is limited and only allows gross comparisons; even with those limitations, the UK data seem concerning. Pneumonia and myocarditis may be more important than agranulocytosis in explaining the uneven distribution of fatal outcomes in clozapine patients across countries.
| Original language | English |
|---|---|
| Pages (from-to) | 239-245 |
| Number of pages | 7 |
| Journal | Journal of Clinical Psychopharmacology |
| Volume | 43 |
| Issue number | 3 |
| DOIs | |
| State | Published - May 1 2023 |
Funding
In the last 3 years, G.S. has served as a consultant for HLS Therapeutics and Thermo Fisher. S.H.K. has received research grants from and/or served as a lecturer for Janssen, Otsuka, Eli Lilly, and Dongwha. R.O.C. is a speaker for Clinical Care Options; has received research funding from Otsuka, Lundbeck, Roche, and Alkermes; and has received consulting fees from Saladax Biomedical; S.R.C. has participated in advisory and educational boards and received speaker's fees from Janssen-Cilag, Lundbeck, Otsuka, and Servier; research funding from Janssen-Cilag, Lundbeck, Otsuka, and Gilead; and data sharing from Viatris Australia. A.W. received research funding from Biogen and Janssen-Cilag. M.S. participated in lectures for the following companies: Alkaloid, Belupo, Eli Lilly, Gedeon Richter, Jadran Galenski Laboratorij, Johnson/Johnson, Lundbeck, Pliva, and Stada, and participated in the clinical trial: Eli Lilly, Krka, and Gedeon Richter. A.E.A.Y. has participated in advisory boards and received speaker's fees from Janssen and Abdi İbrahim Otsuka, and has received investigator fees from Janssen. D.I.R. served as a lecturer for Goodwill Pharma, Richter Gedeon, Teva Srbija, Krka, Alkaloid, Viatris, and Pharmalogist. The rest of the authors had no conflicts of interest in the last 3 years.
| Funders |
|---|
| Biogen IDEC |
Keywords
- clozapine/administration and dosage
- clozapine/adverse effects
- clozapine/metabolism
- clozapine/therapeutic use
- clozapine/toxicity
- COVID-19
- drug labeling
- infection
- inflammation
- mortality/drug effects
- pneumonia
- schizophrenia
- sex
- smoking
- Humans
- United Kingdom
- Pharmacovigilance
- Agranulocytosis/chemically induced
- Antipsychotic Agents/adverse effects
- Clozapine/adverse effects