# Efficacy and safety of atomoxetine in the treatment of ADHD in children and adolescents: a systematic review

**Authors:** Edmundo Alberto Barbosa Bastos De Souza Neto, Halley Ferraro Oliveira, Williams Santos Ramos, Estelio Henrique Martin Dantas, Barbara Hellen Alves Pereira, Rebeca de Souza Mariano Bastos

PMC · DOI: 10.3389/frcha.2025.1731330 · Frontiers in Child and Adolescent Psychiatry · 2026-01-06

## TL;DR

This study reviews atomoxetine's effectiveness and safety for treating ADHD in children and adolescents, finding it comparable to other medications.

## Contribution

The paper provides a systematic review comparing atomoxetine with other ADHD treatments, focusing on its role for patients who cannot tolerate stimulants.

## Key findings

- Atomoxetine showed comparable efficacy to methylphenidate in reducing ADHD symptoms.
- Common side effects included nausea, fatigue, and appetite changes, with no severe adverse events reported.
- Atomoxetine is a valid alternative for patients who do not tolerate stimulant medications.

## Abstract

To evaluate the efficacy and safety of atomoxetine in the treatment of adolescents with ADHD, comparing its effects with other available treatments. The primary outcome was the reduction of ADHD symptoms, and the secondary outcome was the occurrence of adverse effects.

A search was conducted in the Medline/PubMed, EMBASE, and Web of Science databases. The research question and strategy were based on the PICO model. Inclusion criteria were restricted to studies involving children and adolescents aged 6–16 years, focusing on comparisons between atomoxetine and other treatments. Eligible studies were published in English, Spanish, or Portuguese, with no restrictions on publication year. A total of 575 articles were initially retrieved. After removing duplicates, 527 references were screened by title and abstract, and 69 were selected for full-text review. Following this stage, 63 references were excluded, and 6 studies were ultimately deemed eligible.

The six included studies involved a total of 905 participants. Atomoxetine demonstrated comparable efficacy to methylphenidate in reducing ADHD symptoms. The most common adverse effects were nausea, fatigue, and appetite changes. No severe adverse events were consistently reported. Atomoxetine's efficacy was particularly evident in patients who did not tolerate or respond to stimulant medications.

Available evidence suggests that atomoxetine is an effective and safe option for treating ADHD in adolescents, representing a valid alternative particularly for patients who do not tolerate stimulant medications. Continued research, especially long-term studies, is necessary to confirm its efficacy across different patient subgroups.

Identifier CRD420251152121.

## Linked entities

- **Chemicals:** atomoxetine (PubChem CID 54841), methylphenidate (PubChem CID 4158)
- **Diseases:** ADHD (MONDO:0007743)

## Full-text entities

- **Diseases:** nausea (MESH:D009325), ADHD (MESH:D001289), fatigue (MESH:D005221)
- **Chemicals:** Atomoxetine (MESH:D000069445), methylphenidate (MESH:D008774), stimulant medications (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12816204/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12816204/full.md

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Source: https://tomesphere.com/paper/PMC12816204