Prozac No Better Than Placebo for Child Depression, Study Finds
Prozac no better than placebo for children

Landmark Study Questions Prozac's Effectiveness for Young People

Medical experts are calling for an immediate overhaul of clinical guidelines after groundbreaking research revealed that the antidepressant Prozac shows no meaningful benefit over placebo drugs when treating depression in children and adolescents. The comprehensive analysis, conducted by international researchers, suggests that continuing to prescribe this medication exposes young people to potential harm without offering any clinical advantage.

Concerning Evidence from Global Trials

Researchers from Austria and the UK conducted a detailed meta-analysis of 12 major clinical trials published between 1997 and 2024, all examining fluoxetine's effectiveness. Sold under the brand name Prozac among others, this medication is commonly prescribed worldwide. The study, published in the Journal of Clinical Epidemiology, reached a startling conclusion: any improvement in depressive symptoms was so minimal that it couldn't be considered clinically meaningful.

Lead author Martin Plöderl, a clinical psychologist at Paracelsus Medical University in Salzburg, offered a powerful analogy: "Consider the analogy of a weight-loss drug that is better than placebo at producing weight loss, but the difference is only 100 grams. This difference is unlikely to be noticeable to the patient or their doctors or produce any difference in their overall condition."

The Hidden Dangers and Urgent Call for Change

The research identified a "novelty bias" in earlier trials, which showed more positive results that later studies failed to replicate. More alarmingly, the study emphasises that the known risks of fluoxetine likely outweigh its negligible benefits. Children taking antidepressants commonly experience significant side effects including weight gain, sleep disturbances, concentration problems, and increased suicidal ideation.

Co-author Mark Horowitz, an associate professor of psychiatry at Adelaide University, stated unequivocally: "Fluoxetine is clearly clinically equivalent to placebo in its benefits, but is associated with greater side effects and risks. It is difficult to see how anyone can justify exposing young people to a drug with known harms when it has no advantage over placebo in its benefits."

The researchers also examined guidelines in the US and Canada, finding they similarly ignore this evidence and continue recommending Prozac for young patients. With global mental health statistics showing one in seven 10-19 year olds experience mental health conditions, and UK figures indicating up to a quarter of older teenagers struggle with anxiety or depression, this issue affects millions worldwide.

While a Nice spokesperson defended current guidelines, emphasising the importance of having multiple treatment options, the research team maintains that clinical practice must align with the latest evidence to protect vulnerable young people from unnecessary medication risks.