Advice

following a full submission

atomoxetine (Strattera®) is accepted for use within NHS Scotland.

Indication under review: treatment of attention-deficit/hyperactivity disorder (ADHD) in adults as part of a comprehensive treatment programme. The presence of symptoms that were pre-existing in childhood should be confirmed.

Short term studies in adults have shown that atomoxetine improves symptoms of ADHD compared to placebo. 

The economic case for atomoxetine has been demonstrated for a treatment duration of one year.

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Medicine details

Medicine name:
atomoxetine (Strattera)
SMC ID:
909/13
Indication:
Treatment of attention-deficit/hyperactivity disorder (ADHD) in adults as part of a comprehensive treatment programme. The presence of symptoms that were pre-existing in childhood should be confirmed.
Pharmaceutical company
Lilly UK
BNF chapter
Central nervous system
Submission type
Full
Status
Accepted
Date advice published
11 November 2013