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Int J Risk Saf Med ; 31(4): 259-265, 2020.
Article in English | MEDLINE | ID: mdl-32145001

ABSTRACT

BACKGROUND: Disease-modifying therapies for multiple sclerosis have been developed tremendously over the last two decades. OBJECTIVE: The aim of this study was to review the short-, medium-, and long-term safety of alemtuzumab in relapsing remitting multiple sclerosis (RRMS). METHOD: This retrospective observational study (2015-2019) included all patients with highly active or rapidly progressing and aggressive RRMS who were treated with alemtuzumab at the Cabueñes University Hospital. The short-, medium-, and long-term adverse effects were evaluated following the risk management program of the European Medicines Agency. RESULTS: 39 patients were included, 23 of them received at least two cycles of treatment. Most patients showed at least one adverse event. The following adverse reactions were reported: infusional reactions (17), urinary tract infections (six), thrombopenia (five), and thyroid dysfunction (six). CONCLUSION: In clinical practice alemtuzumab showed an acceptable safety profile in selected patients even if all of them suffered at least one adverse effect. Thorough and prolonged follow-up is required to further confirm the safety of this drug.


Subject(s)
Multiple Sclerosis, Relapsing-Remitting , Multiple Sclerosis , Alemtuzumab/adverse effects , Humans , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Recurrence , Retrospective Studies
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