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Latest News Around the Web

FDA Panel Discusses Safety Of SSRI Use During Pregnancy

The New York Times (7/21, Barry ) reports, “Over nearly four decades since Prozac [fluoxetine] was approved for the treatment of depression, waves of concern about the effects of antidepressants during pregnancy have resulted in a practical consensus: Though use of the drugs may be associated with a slight rise in the odds of birth defects, the risk of leaving a mother’s depression untreated is often greater.” Now, among a “select group of experts convened by the Food and Drug Administration on Monday to discuss the safety of antidepressants during pregnancy, around half said that women should receive a more clear and forceful warning about potential risks to the fetus.” HHS spokesperson Andrew Nixon “said the agency would not comment on whether there were plans to require a so-called black box warning about the use of selective serotonin reuptake inhibitors, or SSRIs, in pregnancy.”

MedPage Today (7/21, Monaco ) reports, “Women should be better informed about the potential risks of using selective serotonin reuptake inhibitors (SSRIs) during pregnancy, and these risks should be weighed against their benefits, most speakers on an FDA panel selected by Commissioner Marty Makary, MD, MPH, agreed on Monday.” Makary said, “Up to 5% of women in pregnancy are on an antidepressant. Antidepressants like SSRIs can be an effective treatment for depression.” However, “he warned that SSRIs ‘may be unique’ because of their potential interaction with pregnancy.”

NBC News (7/21, Bendix ) also reports.

Related Links:

The New York Times (requires login and subscription)

FDA Adviser Panel Votes Against Efficacy Of Otsuka’s Combination Treatment For Adults With PTSD

Reuters (7/18, Sunny, Mahatole) reported the FDA’s “panel of independent advisers on Friday voted against the efficacy of Otsuka Pharma’s antipsychotic drug in combination with Viatris’ antidepressant Zoloft [sertraline hydrochloride] for treating adults with PTSD.” The FDA “panel voted 10-1 to say the available data does not establish the efficacy of the drug, brexpiprazole, in combination with Zoloft…for treating the condition.” The panel’s “decision is in line with the FDA staff reviewers’ assessment on Wednesday.

Related Links:

— “US FDA advisers recommend against Otsuka’s PTSD combination treatment,”Mariam E Sunny and Siddhi Mahatole, Reuters, July 18, 2025

Some Women Face Greater Risk Of Depression As They Go Through Premature Menopause, Study Suggests

HealthDay (7/18, Thompson ) reported, “Some women have a greater risk of depression as they go through premature menopause, according to a new study.” Researchers found that “women were at greater risk for depression if they entered premature menopause earlier; their condition had a genetic cause; or they experienced worse menopause symptoms.” Study results indicate that “women grieving the loss of their fertility or without sufficient emotional support also had a higher risk.” The findings were published in Menopause.

Related Links:

— “Depression Risk Greater In Some Women With Premature Menopause,”
Dennis Thompson , HealthDay, July 18, 2025

988 Suicide & Crisis Lifeline’s Specialized Services For LGBTQ+ Youth Have Ended Operations

CNN (7/17, Howard ) reports, “The 988 Suicide & Crisis Lifeline’s specialized services for LGBTQ+ youth have officially ended operations, meaning people contacting 988 for help no longer have the option to ‘press 3’ to reach counselors specifically trained to respond to the needs of this group.” According to CNN, “The lifeline included a subnetwork for LGBTQ+ youth soon after its launch in July 2022.” However, “the US Department of Health and Human Services’ Substance Abuse and Mental Health Services Administration…announced last month that those services would be coming to an end.”

Related Links:

— “Trump administration ends 988 Suicide & Crisis Lifeline’s specialized service for LGBTQ+ youth,”Jacqueline Howard , CNN, July 17, 2025


Most Individuals Do Not Go Through Severe Withdrawal After Discontinuing Antidepressants,Study Suggests

HealthDay (7/17, Gotkine ) reports, “Most individuals do not go through severe withdrawal after discontinuing antidepressants,according to a study.” One researcher said, “Despite previous concern about stopping antidepressants, our work finds that most people do not experience severe withdrawal, in terms of additional symptoms. Importantly, depression relapse was not linked to antidepressant withdrawal in these studies.” The findings were published in JAMA Psychiatry.

Related Links:

— “Few Discontinuation Symptoms Reported After Stopping Antidepressants,”
Elana Gotkine , HealthDay, July 17, 2025

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