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Debate Intensifies Over SSRI Risks for Pregnant Women
27 Aug
Summary
- FDA panel debates black-box warning for SSRIs
- Maternal mortality a leading cause of pregnancy-related deaths
- Experts divided on weighing SSRI risks vs. benefits

In the past month, a U.S. Food and Drug Administration panel has been debating whether SSRIs (selective serotonin reuptake inhibitors), a class of antidepressants, should carry a black-box warning. This debate has unfolded against the backdrop of the country's stubborn maternal mortality rate, which remains among the highest in the developed world. Mental health conditions are now the leading cause of pregnancy-related deaths occurring up to a year after childbirth.
The panel's discussion has prompted a backlash from doctors and professional groups, who argue that the risks of SSRIs cannot be examined in isolation, but must be weighed against the risks of untreated depression. Experts note that it is challenging to assess medication safety in pregnant women, as randomized controlled studies are typically not conducted due to ethical concerns. Instead, scientists must rely on observational studies, which make it difficult to disentangle the effects.
While some studies have suggested an increased risk of negative health outcomes like congenital malformations, more recent, higher-quality research indicates that any risk is likely minimal. Ultimately, experts say the benefits of SSRI use for women with severe depression appear to outweigh the potential risks. However, others, like Dr. Adam Urato, argue that this is a "chemical-exposure problem" that can have impacts on fetal development.
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The debate continues, with doctors acknowledging the difficult balance between the risks and benefits of SSRI use during pregnancy. As one patient, Barbara Akman, shared, the decision to stay on antidepressants was not an easy one, but she ultimately felt it was the best choice for her and her family.