Saturday, January 24, 2015

The Curse of Akathisia

A small but important percentage of people who take antidepressants, antisychotics, and certain other meds (like prochlorperazine, used for vertigo, nausea, and migraine) tend to develop a very serious reaction called akathisia, which, in severe cases, is responsible for suicide, homicide, and self-harm.

I urge you to educate yourself on this bizarre condition, because odds are, your clinician is not well trained in recognizing it, and most patients are unaware of its implications.

Older psychiatrists who grew up in the era of "mental institutions" and neuroleptics are familiar with akathisia (properly so-called), but modern scientific literature reflects an incomplete, fuzzy understanding of it, and we see the result in courtrooms across the UK and US. We're caught off guard when a patient with a bad reaction to a drug experiences an abrupt change of personality and kills himself (or his family) as a result of akathisia. Somehow, this happens over and over again, and each case is seen as a fluke, something that's outside the realm of known medicine, when in fact there's a long precedent in history, medicine, and law for this syndrome.

We need to stop thinking of "the guy who went berserk after taking Prozac" (or Zoloft, or Seroquel, or what have you) as mysterious flukes, mere "anecdotal" incidents that defy rational explanation. We need to look at something like Robin Williams' sudden decision to take his life, eight days after starting Seroquel, and ask: Is there precedent for this? Does it conform to anything we know about these drugs? Is it a known type of adverse outcome?

I guarantee that after you, yourself, have either experienced akathisia, or personally witnessed someone having this reaction, you will know that it is a very real thing. It may be rare, but it exists. My wife experienced it and I almost called 9-1-1 several times, until we figured out which medication was causing it (Latuda) and discontinued the med. Within 24 hours, her symptoms went away. I'm capable of having (indeed, eager to have) my mind changed on a lot of things, but no one will ever convince me that akathisia is not real.

Ladislav Haskovec, who first described akathisia in 1901, considered akathisia to be a kind of hysterical reaction, but R. Bing (in a 1939 textbook on nervous conditions) characterized akathisia as a type of "psychosis" involving "morbid fear of sitting down." Hodge (1959) said that akathisia "may appear like an anxiety state . . . in which real anxiety can be neither recognized nor verbalized." Raskin (1972) recognized that patients often are unable to distinguish bctwecn anxiety and restlessness, and warned that "indications of anxiety-like symptoms" such as "uneasiness," hyperactivity, pacing, "vague complaints about medication," and insomnia may actually be reflective of akathisia.

Van Putten, in his classic paper on akathisia, noted that in patients with florid psychosis, the patient may be unable to articulate dysphoric symptoms properly ("making the diagnonsis especially difficult") and can confuse the symptoms of akathisia with those of the original condition for which the patient is being treated. (How, then, can akathisia be reliably diagnosed? For Van Putten, the test was simple: If the patient's restlessness went away with an injection of 5 mg of the anti-Parkinson's drug biperiden, it was akathisia.) Van Putten's patients tell the story better. They experienced fright, terror, anxiety, and rage, and sometimes beat their head against the wall. "I'm frantic. I just can't get my emotions under control. All of a sudden I feel terrified and want to run." "I feel hostile and I hate (with intense affect) everybody." "My nerves are just jumping." "I just feel on edge; I feel nasty; I feel like jumping out of my skin; if this feeling continues, I would rather be dead."

Kalinowsky (Am J Psychiatry. 1958 Oct;115(4):294-8) observed that akathisia can be "more difficult to endure than any of the symptoms for which [the patient] was originally treated." He cautioned that it could be mistaken for "agitated depression."

Fouks ("Le Syndrome d'impatience," 1968) found that akathisia is associated with severe anxiety, peculiar body sensations, and bizarre mentation.

Akathisia reactions are why Thorazine so quickly fell out of use when additional neuroleptics were developed. Subsequent neuroleptics were "better tolerated" largely because they were less apt to induce akathisia.

The antihypertensive reserpine began to replace Thorazine in 1954. But it was associated with an increased rate of suicide—in the hypertensive patients for whom it was prescribed, rather than in the psychiatric patients to whom it was given in higher doses (Healy and Savage, 1998). Its use was associated with "depression," which was induced in at least 10% of patients who took it. The claims for reserpine-induced depression came primarily from physicians rather than from psychiatrists, however, and it is possible non-psychiatrically-trained physicians were seeing akathisia rather than depression per se. Healy and Savage note:
But another state could appear within hours or days of treatment commencing. This was characterised as follows: "increased tenseness, restlessness, insomnia and a feeling of being very uncomfortable" (Achor et al, 1955), "the first few doses frequently made them anxious and apprehensive . . . they reported increased feelings of strangeness, verbalized by statements such as 'I don't feel like myself' . . . or 'I'm afraid of some of the unusual impulses that I have"' (Faucett et al, 1957). Sarwer-Foner & Ogle (1955) describe the case of a subject who on the first day of treatment reacted with marked anxiety and weeping and on the second day "felt so terrible with such marked panic at night that the medication was cancelled."
Such reactions were interpreted by some as evidence for the then-current theory that patients with essential hypertension actually had a suppressed rage. At least one researcher (Ayd, 1958) considered the syndrome "pseudo-depression" and commented on "motor restlessness which made their muscles taut, compelled them to pace the floor and did not permit them to sit without moving their legs."

M. Katherine Shear and colleagues (1983) reported on suicides that had accompanied use of the antipsychotic fluphenazine. Two years later, Schulte (1985) reported on suicide and homicide associated with akathisia. Other reports followed.

With the introduction of SSRIs (selective serotonin reuptake inhibitors; e.g., Prozac, Zoloft), the spectre of akathisia revived anew. Welsh psychiatrist David Healy tells the story of how, in early 1983, almost a decade before it launched in the US, a study of Zoloft (sertraline) was undertaken by Dr. Ian Hindmarch in Leeds, UK, using healthy volunteers. Healthy-volunteer studies are typically part of Phase I trials, to show basic safety. In such studies, non-symptomatic, illness-free volunteers simply take a new drug for up to a week just to show that there are no ill effects. In the Hindmarch protocol, there were 12 female volunteers aged between 34 and 40; the study was supposed to randomize half its subjects to sertraline and half to placebo, for a week, followed by a crossover between drugs. The study was abandoned before the first week was out (and never published). According to Healy:
The medical report to Pfizer noted that the side effects reported in the study were all elicited independently, without communication between participants, that there was a clearcut difference in side effect reporting between placebo and sertraline, and that the volunteers on sertraline were experiencing marked discomfort. The study was accordingly terminated.

All of the sertraline subjects had problems, as had one of the placebo subjects. The placebo subject having problems, however, had sertraline levels in her blood, making the finding even more convincing. The side effects that seemed most clearly linked to sertraline were apprehension, insomnia, movement disorders, and tremors.
Apparently, one of the placebo subjects had just begun the crossover part of the experiment, going from placebo to sertraline; that's when her problems began.

Rothschild and Locke (1991) described three patients who became suicidal on fluoxetine (Prozac), then discontinued the drug, then were reintroduced to fluoxetine—and immediately became suicidal again. Said the researchers: "All three patients developed severe akathisia during retreatment with fluoxetine and stated that the development of the akathisia made them feel suicidal and that it had precipitated their prior suicide attempts. The akathisia and suicidal thinking abated upon the discontinuation of the fluoxetine or the addition of propranolol."

Hamilton and Opler (1992) described a link between SSRIs (specifically, fluoextine: Prozac), akathisia, and suicidality. They noted:
Several reports already exist in the literature documenting the development of EPS [extrapyramidal symptoms] in association with fluoxetine, but without necessarily linking this to an increased incidence in suicidal ideation. Specifically, Lipinski et al. first reported the occurrence of akathisia in five patients treated with fluoxetine. Bouchard et al. reported that EPS developed in several of their patients while they were being treated with fluoxetine and in other patients the baseline levels of EPS worsened during fluoxetine treatment. Symptoms noted included bradykinesia, cogwheel rigidity, and akathisia. Tate reported that a patient who had previously tolerated haloperidol alone had an increase of EPS (including parkinsonism and akathisia) when fluoxetine was added. Stein reported a case of tardive dyskinesia that developed when a low dose of haloperidol was added to fluoxetine. In the case reported by Teicher et al., four of the six patients described complained of an inner restlessness which Opler has previously argued could reflect that they were experiencing akathisia. Wirshing et al. recently reported that five patients treated with fluoxetine experienced ‘agitation, restless motor movement, dysphoria, pacing, an internal sense of desperation, and suicidal ideation,’ and they too suggest ‘that fluoxetine-induced akathisia can lead to suicidal ruminations.’
The literature on akathisia and suicide (and the connection to SSRIs) is fairly extensive and has been summarized by Healy here. In addition, David Healy and Chris Whitaker, in 2003, published an extensive review of suicidality vis-a-vis SSRIs in the Journal of Psychiatry and Neuroscience, in which (quite aside from demonstrating some alarming risk ratios) they tease apart some very important and often-missed issues with regard to the drug makers' tallying of adverse events at various phases (including the "washout" phase) of clinical trials. They point out that 5% of study participants typically report "anxiety" or "agitation" (no patient ever reports akathisia, since it's a term known only to specialists). Also, they note that the drug makers have often customarily, and quite deliberately, prescribed benzodiazepines (e.g., Xanax, Valium, Klonopin) to study participants, to minimize the agitation that's known to occur in some people taking SSRIs. (What's that? You didn't know that drug makers confound their own study results by prescribing other psychoactive drugs concurrently, during trials? Welcome to the real world.)

In antidepressant trials, over the years, side effects involving akathisia have routinely been conflated with "anxiety," "agitation," "restlessness," "insomnia," and other easy-to-score symptoms. (Note that many line employees at the clinical research organizations that carry out these studies are ill trained to recognize akathisia, per se, in study participants.) Combine this with the fact that only a fraction of people with side effects ever bother to complain about them (the true ratio is often considered to be one-in-ten), and you have a formula for disaster.

The literature on suicidality and SSRIs is either clearcut (in favor of SSRIs reducing suicidal behavior) or not, depending on what you read. The extraordinarily exhaustive 2005 literature review by Fergusson et al. in BMJ (which everyone should read) found an increased risk of suicidal behavior, but not completed suicides, for SSRI users. One way to understand such results is to consider the possibility that what we're looking at are two population subsets that produce countervailing results. On the one hand, we have a subpopulation of patients for whom SSRIs work; and these people probably commit fewer suicides. On the other hand, we have a subpopulation of patients for whom these drugs produce a spectrum of "agitation" effects, including (in predisposed individuals) full-on akathisia. The latter commit suicide, or attempt to. Combine the subpopulations, and the net result is an increase in suicidal behaviors, but not actual suicides.

But suicide isn't the only problem.

In a 2006 report in PLoS Medicine, we learn of the case of DS, a 60-year-old man with a history of five prior anxiety/depressive episodes, none of which involved suicidality or aggressive behaviour. His prior episodes had resolved within several weeks. In 1990, DS had an episode of depression, which his doctor treated with fluoxetine (Prozac). The man had a clear adverse reaction to fluoxetine involving agitation, restlessness, and possible hallucinations, which worsened over a three-week period despite treatment with trazodone and propranolol (which should have mitigated such reactions). After fluoxetine was discontinued, DS responded rapidly to imipramine.

In 1998, a new family doctor, unaware of his adverse reaction to fluoxetine, prescribed paroxetine (Paxil, an SSRI), 20 mg daily, for DS, for what was diagnosed as an anxiety disorder. Two days later, having had two doses of the medication, DS used a gun to put three bullets each through the heads of his wife, his daughter who was visiting, and his nine-month-old granddaughter, before killing himself.

At the jury trial in Wyoming in June 2001, a jury found that paroxetine “can cause some people to become homicidal and/or suicidal.” SmithKline Beecham was deemed 80% responsible. The documentary evidence at the trial included an unpublished company study of incidents of serious aggression in 80 patients, 25 of which involved homicide.

Many additional "anecdotal reports" exist. We can add actor/comedian Robin Williams to that list; he had just begun taking the antipsychotic Seroquel eight days before he hung himself in 2014.

These are all "just anecdotes" until they actually happen to someone you know.

Don't kid yourself. Akathisia is real. The body count says so.

This post was adapted, in part, from a book I'm writing on mental illness. Please add your name to the mailing list to be notified when the book and free sample chapters become available. Thank you, and please, if you know someone who can benefit from this kind of information, tell him or her about the book and this blog. Thanks so much.


  1. During an inpatient hospital stay, my psychiatrist prescribed risperidone. I had not taken this medication before. Within a short amount of time of taking the first dose, I found that I was having trouble sitting and staying still. It felt like I was coming out of my skin. I didn't say anything to the doctor or staff that day. I was sure it was my imagination. I made it through by walking a lot on the unit. Back and forth. Back and forth. After I took the second dose the next morning, the feeling was twice as strong. This time, I said something to my doctor. I couldn't describe it very well. I told him I couldn't sit for any length of time. I had to be asleep or walking. My brain felt like it was stuffed with tissue paper. At that time, I did not know the word "akathisia," and my doctor did not mention it as a possibility. I finally refused the drug a few days later because I couldn't cope with the physical sensations any longer. Luckily, the drug cleared my system fairly quickly, and a few days later, I began to feel like a real human being again. I have not experienced it again.

    This happened more than five years ago, but my psychiatrist and I have never talked about this side effect. I don't fault my doctor. He's usually very informative about medication. But if I'd known ahead of time what akathisia was, I would have known right away that something wasn't right. The lesson I learned was not to assume that a new, strange physical sensation is my imagination, especially when it coincides with starting a new drug.

    1. Thank you for this input. It fits the akathisia pattern. Usually, the last thing anyone suspects is that the medication is to blame, because the default assumption is that medication can only help. Your final sentence says it all.

  2. I first experienced akathisia after an overdose of fluoxetine and several anti anxiety and other pills, I woke up in hospital unable to even tolerate eating toast. Once home I had to jog around outside, I cried, jumped, nothing eased the sensation, sleep (once finally able to) was the only escape. I thought is was a crazy one off effect of so much medication.
    I was sadly wrong, couple of years later starting depakote I had the same unease, thankfully milder, but even sitting through 10 mins of TV was mental hell. Latuda did the same. I managed to find out it was a real thing by researching it myself on google. Oh the relief and frustration that no one seemed to know what it was all about!!
    Yesterday I was forced to take risperidone as I'd been awake 62hrs and had no plans of sleep, it worked.. but I'm petrified I'll feel this again in case no one believes me!

    Thankyou for writing about it and how seriously unpleasant it can be, I would rather staple my eyelids to my forehead than have to cope with this feeling for any length of time!!!!!

  3. I experienced akathesia for 3 days after starting abilify for cyclothymia. Its the scariest thing ive ever experienced. It stopped about 12 hours after abilify was withdrawn by A&E doctor. There should be a black box warning about this side effect.

  4. If akathesia persist how to dealt with the problem my son is facing same situation as described by you. And doctor is also not able to control it. He again started quitipin.

  5. If akathesia persist how to dealt with the problem my son is facing same situation as described by you. And doctor is also not able to control it. He again started quitipin.

  6. I am also writing a book on mental illness and I am dedicating a whole chapter to my experience with akathisia. I had a single test dose injection of flupenthixol and had akathisia for months. It was by far the single worst thing I have ever experienced in my whole life. It caused my first proper suicide attempt. I still have nightmares about it. I would do anything to raise awareness of this problem and it's severity.

  7. I agree. 5 years and still suffering with it and thinking of suicide. It's a horrible beast of a disease that makes psychosis look tame. It's pure, unadulterated agony.

  8. Thank you for this. I have chronic Akathisia. I guess that incredibly rare, as most people's akathisia goes away. It's a nightmare of screaming and pulling on my hair and I rock in the couch. What purpose do I have in life?

    It took family and God to help me through. I still have my suicide plan for backup, but I suppose since I've made it this long I can make it to the end. I hope I die young so it will go away. I don't do monograms or colonoscopies, don't follow my diabetic diet and I will never pervent cancer from ravaging my body. When I did, I die. I will have given my and that's all most of us can do. Thank you for writing this. I have Akathisia from Paxil, Seroquel and Abilify. It was made worse by Requip, arrange and lyrica.

    1. My heart hurts for you. I am so sorry. I have been suffering for 6 years from Latuda. Now, as I taper off of it, the akathisia seems to be getting worse every day. My doctor seems to think that's strange, but hello? I'm coming OFF LAtuda, and why wouldn't that cause it as well as being on it? I remember coming off of Pristiq and the withdrawals lasted forever. Now I look back, it was severe akathisia made even worse by withdrawals. I understand the death wish. I do it all the time. When I'm driving, I almost feel a sense of peace knowing someone could hit me and kill me. Then my kids wouldn't have to deal with me taking my own life. This is no way to live. I have been describing this unbearable "agitated depression" to my psychiatrist for 6 years and never once did he mention it could be akathisia. My neuropsychologist was the one who finally caught on. The fact that it was medically induced and not organic makes it all the more unbearable for me. I hear you, I understand and all I can say is you aren't alone in your suffering. ANd I know that doesn't help at all.

  9. My husband has now had akathisia for 2.7 years. Here is his video explaining what part of it (minus the mental part) is like for him

    1. OH and we have a support group on Facebook for anyone needing support. You can search "Living with Akathisia" and find us

  10. One 10mg dose of Lexapro left me with permanent brain damage and episodic akathisia. I have suffered with this for 10 years.

    1. Once a person has experienced this horrific sensation, it is immediately understandable why those with this affliction commit suicide.

  11. I have had varying degrees of akathisia from two different medications. The first one was Latuda. I did not recognize the sensation at first but it was relatively mild. When I went from 60 mg to 80 mg it became a cute and severe. I had to straighten my entire body and scream every 15 seconds while driving just to get to my next destination.The onset was about 30 minutes after taking Latuda at about 6 AM in the morning, and it was that incident where I became certain of what was happening.I had to take 4 mg of Xanax to knock me out. Fortunately when it occurs I am able to sleep it off. That scared me so bad that I never took Latuda again.

    Now Saphris. The trend I am noticing is that akathisia his present almost every time I take any of these medications, but I am to take them at night and I typically sleep through it. Whenever I take these medications during the day I suffer from this side effect. Sometimes in a very severe manner.

    I am still sorting out the one medication I’m going to take, when I am going to take it, etc. I will probably stick with the Saphris and try only taking it at night when I am ready for sleep. That seems to work but it is terrifying to lat there knowing that if you do not fall asleep, you could suffer from an episode of akathisia.

    This is one of the most harrowing and terrifying things you could ever experience. I have no idea how people live with this long term. If I had to endure more than a handful of hours I would not stay with this world. Absolute , unfiltered horror and agony.

    I am convinced that many episodes where people become violent toward others or hurt themselves are related to this condition that seems like a bit of an enigma, especially if you have not experienced it. I have been fortunate to be around people who were patient and loving, or alone, each time. If I were around people that were triggering me and did not understand what I was going through I would probably lose it. Scary stuff.


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