What do systematic reviews say?

Grades 3 and 4 adverse events ‐ not reported · outpatients withmild disease

Withdrawals due to adverse events ‐ not reported · participants with quiescent IBD

Withdrawals due to adverse events ‐ not reported · participants with quiescent IBD

Adverse events at post‐treatment ‐ not reported · adults with anxiety disorders

Adverse events post‐intervention ‐ not reported · patients with fibromyalgia

Adverse events post‐intervention ‐ not reported · patients with fibromyalgia

Adverse events post‐intervention ‐ not reported · patients with fibromyalgia

Withdrawals due to adverse events ‐ not reported · people with chronic gout

WIthdrawals due to Adverse Events ‐ not reported · patients with shoulder pain

Adverse events associated with PET ‐ not reported · Individuals with Hodgkin lymphoma

Incidence of serious adverse events ‐ not reported · adults with alopecia areata

Incidence of serious adverse events ‐ not reported · adults with alopecia areata

Specific adverse events: haemorrhage · women with recurrent or FIGO stage IVB cervical cancer

Withdrawal due to serious adverse events Not reported · patients with rheumatoid arthritis

Withdrawal due to serious adverse events Not reported · patients with rheumatoid arthritis

Withdrawal due to serious adverse events Not reported · patients with rheumatoid arthritis

Adverse events: serious adverse events ‐ not reported · patients with schizophrenia

Number of women reporting adverse events ‐ not reported · women with urinary incontinence

Number of women reporting adverse events ‐ not reported · women with urinary incontinence

Number of women reporting adverse events ‐ not reported · women with urinary incontinence