Adverse Events in NMOSD Therapy.
Katrin GiglhuberAchim BerthelePublished in: International journal of molecular sciences (2022)
Neuromyelitis optica spectrum disorders (NMOSD) are rare neurologic autoimmune diseases that have a poor prognosis if left untreated. For many years, generic oral immunosuppressants and repurposed monoclonal antibodies that target the interleukin-6 pathway or B cells were the mainstays of drug treatment. Recently, these drug treatments have been complemented by new biologics developed and approved specifically for NMOSD. In principle, all of these drugs are effective, but treatment recommendations that take this into account are still pending. Instead, the choice of a drug may depend on other criteria such as drug safety or tolerability. In this review, we summarise current knowledge on the adverse effects of azathioprine, mycophenolate mofetil, rituximab, tocilizumab, eculizumab, satralizumab, and inebilizumab in NMOSD. Infections, cytopenias, and infusion-related reactions are most common, but the data are as heterogeneous as the manifestations are diverse. Nevertheless, knowledge of safety issues may facilitate treatment choices for individual patients.
Keyphrases
- poor prognosis
- healthcare
- long non coding rna
- drug induced
- randomized controlled trial
- rheumatoid arthritis
- emergency department
- low dose
- adverse drug
- newly diagnosed
- open label
- systemic lupus erythematosus
- clinical trial
- big data
- study protocol
- peritoneal dialysis
- patient reported outcomes
- smoking cessation
- rheumatoid arthritis patients