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. 2023 Oct 4;9(4):20552173231204466. doi: 10.1177/20552173231204466

Table 3.

Adverse events leading to natalizumab treatment discontinuation (total study cohort, n = 72).

Adverse event Number of patients
n %
Airways, lungs, thoracic cavity, and mediastinum
Dyspnea 1 1.4
Upper airway infection 2 2.8
Alimentary tract
Abdominal pain 2 2.8
Blood and lymphatic tissue
Anemia 1 1.4
Leukocytosis 1 1.4
Neutropenia 1 1.4
Thrombocytopenia 1 1.4
Bone, skeletal muscle, and connective tissue
Backache 2 2.8
Flank pain 1 1.4
Limb pain 3 4.2
Muscle spasticity 1 1.4
Muscle weakness 4 5.6
Occipital pain 1 1.4
Cardiovascular
Deep venous thrombosis 1 1.4
Palpitation 1 1.4
Tachycardia 1 1.4
General
Chest pain 1 1.4
Fatigue 3 4.2
Fever 2 2.8
Headache 1 1.4
Shivering 1 1.4
Immune system
Anaphylactic reaction 1 1.4
Mild allergic reaction 10 13.9
Infections
Abscess (not at site of injection) 1 1.4
Progressive multifocal leukoencephalopathy (PML) 2 2.8
Unknown infection 4 5.6
Liver and biliary system
Abnormal liver function test 6 8.3
Hepatic insufficiency 1 1.4
Hyperbilirubinemia 1 1.4
Nervous system
Cognitive disorders 1 1.4
Tremor 1 1.4
Skin and subcutaneous tissue
Alopecia 1 1.4
Eczema 4 5.6
Urticaria 4 5.6
Unknown 28 38.9