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cover of episode People say they've faced withdrawals from SSRIs. They want recognition and research

People say they've faced withdrawals from SSRIs. They want recognition and research

2025/6/27
logo of podcast All Things Considered

All Things Considered

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People
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Alan Schatzberg
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Nasir Ghami
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Nick Alves
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Philippa Minari
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Sven Hube
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Philippa Minari: 我在服用Effexor十年后尝试停药,起初几个星期感觉还好。但大约六到九个月后,我开始感到非常糟糕,出现了神经疼痛、颈肩酸痛和极度焦虑等新症状,甚至难以站立。为了获得残疾补助,医生建议我重新服用Effexor,之后我更缓慢地逐渐停药。虽然神经疼痛和疲惫有所好转,但焦虑却变得更糟,我花了两年多的时间才让大脑平静下来,不再24小时都处于恐慌状态。许多医生没有警告我可能发生这种情况,并且在我出现症状时也不相信我。 Nasir Ghami: 我认为重要的是要理解,严重的血清素戒断综合征确实会发生在这些药物上。虽然研究人员已经记录了几十年的案例,但几乎没有对这些情况进行大规模的研究。我们所知道的是,服用这些药物的时间越长,停药时出现问题的可能性就越大。治疗抑郁症很重要,但也许不应该服用这些药物10年、15年、20年、30年。重要的是要缓慢地停药,不要突然停止。 Sven Hube: 我在服用Lexapro后,有一天突然出现了生殖器麻木,并且发展为极端的情感麻木。虽然药物确实改善了我的情绪,但副作用太大了,所以我逐渐停止了服药。停药一年半后,性功能障碍和情感麻木仍然没有消失。我无法与任何家人或朋友产生联系。以前我还有感觉,经常是坏的感觉,但我能感觉到一些东西,现在我什么都感觉不到。我的医生告诉我这都是我的想象,但在网上,我找到了很多有类似经历的人。 Nick Alves: 作为PSSD Network的推广人员,我发现患者倡导团体开始受到关注,最重要的是来自机构的关注。我们刚刚获得了有史以来的第一笔研究经费,这是历史性的。这些是由加拿大政府资助的小型研究经费。 Alan Schatzberg: 美国精神病学协会已经开始关注PSSD问题,原因是有很多遭受痛苦的人们发出了声音。

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A growing number of people say antidepressants have left them with debilitating symptoms years, even decades, after going off the medications. Increasingly, these people are gathering online and pushing for recognition and research. Emily Corwin with APM Reports has the story. It was 2013 when Philippa Minari decided to go off her antidepressant Effexor, which she'd started 10 years earlier. Her doctor oversaw the process of quitting, which took a few weeks. And at first, it was

It was fine. And about six to nine months later, I started feeling horrible. I had nerve pain. My neck and shoulders were sore all the time. My anxiety was through the roof. All of this was new. Minari says she found it difficult just to stand up. To get disability, a doctor told her to go back on the Effexor, which she later weaned off of more slowly.

The nerve pain and exhaustion got better. But, she says, the debilitating anxiety, it got worse. It took over two years for my brain to calm down enough that I'm not panicking 24-7. Minari is one of the tens of thousands of people who have turned to online forums while dealing with long-term consequences from antidepressants. Many say their doctors didn't warn them this could happen and didn't believe them when it did.

But increasingly, these symptoms are gaining recognition by academic psychiatrists like Nasir Ghami at Tufts University. I think it's important to understand that severe serotonin withdrawal syndrome does happen with these drugs. Serotonin withdrawal syndrome. That's what Ghami calls the array of problems that can occur after stopping antidepressants. Researchers have been documenting cases for decades, but virtually no large-scale studies on these conditions exist.

Because of that, experts still disagree on what to call them, how to prevent them, and how common they are. I was just going over this with a colleague recently to potentially try to do a research study on it because we don't know. Gami believes long-term effects like Menari's are probably quite rare. But, he says, severe short-term withdrawal is far more common. What we do know is the longer you take the drugs, the more likely it is you'll have problems going off them.

Gami says treating depression is important. The solution is not for everyone to never take them, but maybe not to be on them for 10, 15, 20, 30 years. To be clear, doctors say don't stop antidepressants cold turkey. It's important to go slow.

Sven Hube in western Germany spent 13 years on antidepressants. He says he developed genital numbness one day after he took his first Lexapro pill. And I also developed extreme emotional numbness. Hube says the medication did help his mood, but the side effects were too much, so he weaned himself off the drug.

He took his last pill a year and a half ago. But the sexual dysfunction and emotional numbness, they haven't gone away. I can't relate to any family members or friends. Before I took it, I had feelings, bad feelings often, but I felt something and now I do not feel anything at all. Hube says his doctor told him this was all in his head. But on the internet, he found forums full of people with similar stories. And these online networks are growing.

Take the subreddit for people with Huba's condition, post-SSRI sexual dysfunction, or PSSD. Five years ago, this Reddit thread had just 1,000 members. Today, 17,000 people subscribe.

Nick Alves does outreach for the nonprofit PSSD Network. He says patient advocacy groups like his are starting to get attention, most importantly from institutions. We just got like our first ever grants, for example. Like that's historic in this. That's huge. These are small research grants funded by the Canadian government. On top of that, Dr. Alan Schatzberg with the influential American Psychiatric Association just told me it has begun looking into the issue.

The reason he gave? Because a bunch of people who were suffering spoke up. For NPR News, I'm Emily Corwin. And that story came from APM Reports.