Toxicity profile of methotrexate in rheumatoid arthritis. A preliminary survey

Adv Exp Med Biol. 1999:455:359-65. doi: 10.1007/978-1-4615-4857-7_55.

Abstract

A number of patients with rheumatoid arthritis attending the Rheumatology Clinic at St Luke's Hospital are currently receiving the drug methotrexate as a second line disease-modifying agent. A survey has been conducted to assess the toxicity profile of methotrexate in 33 of these patients who were followed up for at least 1 year or until they developed side effects necessitating discontinuation of treatment. Adverse effects in this group of patients included haematological ones (6%), asymptomatic elevations of liver enzymes (57%), gastrointestinal (6%) and dermatological side effects (3%). These results have been compared to larger studies performed abroad. Regular monitoring of a complete blood count and liver function tests has helped to detect the more serious side effects of methotrexate at an early stage enabling successful intervention in these patients.

MeSH terms

  • Adult
  • Aged
  • Anemia, Macrocytic / chemically induced
  • Antirheumatic Agents / adverse effects*
  • Antirheumatic Agents / therapeutic use
  • Arthritis, Rheumatoid / drug therapy*
  • Exanthema / chemically induced
  • Female
  • Folic Acid / therapeutic use
  • Gastrointestinal Diseases / chemically induced
  • Health Care Surveys
  • Humans
  • Liver / drug effects
  • Liver Function Tests
  • Male
  • Methotrexate / adverse effects*
  • Methotrexate / therapeutic use
  • Middle Aged
  • Pancytopenia / chemically induced
  • Patient Education as Topic
  • Patient Selection
  • Risk Factors

Substances

  • Antirheumatic Agents
  • Folic Acid
  • Methotrexate