Drugs approved for the treatment of multiple sclerosis: review of their safety profile

Expert Opin Drug Saf. 2017 Dec;16(12):1359-1371. doi: 10.1080/14740338.2017.1388371. Epub 2017 Oct 12.

Abstract

Multiple sclerosis (MS) is a chronic immune-mediated inflammatory disorder of the brain and spinal cord characterized by inflammation, demyelination, and axonal degeneration. Area covered: Even though the pharmacological armamentarium for MS treatment is considerably improved in the last 20 years, safety data especially for the second-line and innovative treatments are lacking. In order to analyze the safety profile of drugs used for the treatment of MS, a literature review of pre-marketing, post-marketing studies and case reports was performed. Expert opinion: Nowadays, the numerous drugs approved in the last years for the treatment of MS allow a better control of the disease and a better patient compliance. The main advantages of the new disease-modifying agents for MS (DMTs), in fact, derive from the new oral administration and the prolonged half-life with consequent improvement in compliance compared to first-line therapy which required subcutaneous administrations. However, DMTs can cause serious, sometimes life-threatening or fatal, drug adverse reactions. Due to the lack of safety data and given the recent marketing approval of the last DMTs for MS, observational studies and post-marketing surveillance activities will be necessary in order to improve the knowledge about the safety profile of these drugs and the improvement of their use in clinical practice.

Keywords: Clinical trial; disease-modifying agents; multiple sclerosis; real-world data.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Administration, Oral
  • Half-Life
  • Humans
  • Immunologic Factors / administration & dosage*
  • Immunologic Factors / adverse effects
  • Immunologic Factors / pharmacokinetics
  • Medication Adherence*
  • Multiple Sclerosis / drug therapy*
  • Multiple Sclerosis / physiopathology
  • Treatment Outcome

Substances

  • Immunologic Factors