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Tapering Antipsychotic Medications is a Tedious Balancing Act. Consider the Hyperbolic Reduction Strategy.

By Dr. Eappen

Antipsychotic medication can be lifesaving for many patients. However, in addition to mitigating or eliminating psychotic symptoms, these medications can cause unpleasant, even life-shortening, side effects. 

For this reason or because a patient responds well to treatment experiencing fewer psychotic breaks, many patients and their families become anxious to discontinue the use of medication. While it is possible to taper down antipsychotic treatments safely with the careful guidance of a psychiatrist, in some cases, patients simply stop taking these drugs on their own. This is dangerous.

Stopping or weaning yourself off of an antipsychotic medication without a psychiatrist’s supervision can have dire consequences. So, let’s talk about what it looks like to safely transition off of antipsychotic medications.

Side Effects

Common Side Effects

Before we get into the “how” of tapering down medications, you may be wondering: What are the side effects to look out for? How common are they? Do they outweigh the benefits of taking the medication? 

All antipsychotic medications cause side effects, but, common side effects include:

  • Sedation (which can affect social and vocational functioning) 
  • Low blood pressure (which can cause dizziness and/or falls) 
  • Nervous system issues (e.g., constipation, urinary retention, dry mouth, blurred vision, and sometimes cognitive impairment) 
  • Movement disorders (e.g., tremors, muscle spasms, restlessness), 
  • Metabolic syndrome (a cluster of conditions that include high blood sugar, excess body fat around the waist, and abnormal cholesterol levels)
  • Sexual dysfunction (impairment in arousal, libido, and ability to orgasm)

The severity of any side effects you may experience depends on:

  1. Dosage: higher the dose, the greater the side effect risk.
  2. Frequency of administration: taking the entire dose at bedtime may lead to fewer daytime side effects compared to taking the entire dose every morning, or compared to taking a portion of the dose and spreading it through the day, three times a day.  However, different antipsychotics have different frequency requirements, so not all of them can be customized in this way.  For example, Geodon (ziprasidone) requires twice-daily dosing with 350+ calorie meals; Latuda (lurasidone) can be taken once daily but it needs to be taken with a 350+ calorie meal.  However, Zyprexa (olanzapine), Seroquel (quetiapine), and Risperdal (risperidone) are examples of medications that can either have portions of their total daily dose split AM/noon/night, or the entirety of the daily dose can be taken just once a day, at any time of day.
  3. Type of antipsychotic used: All antipsychotics have similar side effect profiles, but each one has greater risk than the other for a particular type of side effect.  Geodon and Latuda are known for having lower risk of weight gain, but Zyprexa is known for having very high risk.  Latuda is known for having higher risk of movement disorders (muscle twitches, tremors).  Seroquel is known for being very sedating (so typically we instruct taking the entire dose at bedtime).
  4. Amount and dosage of other concurrent medications:  if you already take a medicine that causes sleepiness, then adding an antipsychotic may cause you to feel even sleepier than if you did not have that concurrent medicine.
  5. Age: older age leads to greater likelihood of experiencing side effects
  6. Amount and severity of other concurrent medical conditions: for example, if you suffer from low blood pressure (hypotension), then an antipsychotic may place you at greater risk for falls or dangerously low blood pressure compared to someone whose blood pressure is typically within normal range.

It’s important for patients to discuss any side effects they experience with their psychiatrist so that together they can come up with the best plan of action. It can take time to find the right balance of efficacy of treatment while minimizing side effect burden.

How to Safely Taper

How to Safely Taper Antipsychotic Meds

Surprisingly, there are no published guidelines regarding how and when to taper antipsychotics. Doctors largely rely on a combination of clinical judgement, severity of the patient’s symptoms, past experience with previous patients (or past experience of our superiors whom we learned from in training), and the patient’s wishes to determine when a taper should begin and the speed at which it should happen.

Our Approach:

In our practice, with regard to any psychiatric medicine (whether it be an antidepressant, mood stabilizer, or antipsychotic), we generally advise that patients avoid considering a reduction of their medicine until they’ve experienced at least a one year period where they: 

  • Required no changes to their medicines, 
  • Were compliant with all parts of their treatment plan,
  • Experienced no major psychiatric episodes (mood/psychotic episodes, psychiatric hospitalizations, suicide attempts, etc).

Once a patient who is interested in tapering down has had a full year like this, then we will generally recommend reducing the dose by no more than the smallest tablet size available every 3 to 6 months, until discontinuation. 

If, during this process, we discover that a patient needs a particular dosage to remain stable, we will know with precision exactly where that threshold in dosage lies. This gradual reduction also allows us to quickly reverse course and increase the dosage by just the right amount so we don’t overshoot or undershoot what’s needed.

In addition, a rapid dose reduction can drastically increase the risk of a patient’s original symptoms relapsing, which often requires raising the medication dosage to higher levels than the dose would have been at that time, had we chosen a slower reduction strategy.  In order to avoid taking 1 step forward at the expense of potentially taking three steps back, reducing gradually is key.

The Hyperbolic Reduction Strategy:

According to recent studies, our approach to tapering off psychiatric medications is actually even more conservative than what researchers have found to be safe and effective. In this article, physicians in the UK reported reducing the dosage by 50% every 3-6 months (e.g., risperidone doses taken down from 8 mg to 4 mg, then to 2 mg, etc.). This is what we call a hyperbolic reduction strategy.

Given that the side effects with antipsychotic meds are generally dose dependent, this strategy can afford a combination of significant side effect reduction, especially in the beginning of the tapering process, with high likelihood of maintaining control of symptoms at the same time.

Taking this research into consideration, we know that a patient experiencing especially unpleasant side effects and who meets our one-year requirements above could be tapered off more quickly. For patients looking for the fastest and safest option, we could proceed with the hyperbolic strategy offered here.

Final Thoughts

As psychiatrists, we abide by the Hippocratic Oath — one of the oldest binding documents — which says, “first, do no harm.” No one wants to live with unpleasant side effects, but abruptly stopping your antipsychotic medications is almost certainly not the least harmful action we could prescribe.

Whenever a patient asks to be taken off their psychiatric medications, we’re glad they’re raising the question in the clinical setting.  If you’re concerned you’ve been on too high of a dose of medication for too long, then we’d be happy to discuss the risks and benefits of various dose reduction strategies as they relate to your particular condition.      

About the Author

He is the founder and executive director of the Eappen Clinic, a private outpatient mental health practice in Oak Brook, IL. He has been published in peer-reviewed psychiatric journals and has been quoted as an expert in national publications including The Wall Street Journal and Cosmopolitan. After medical school, Dr. Eappen trained at the University of Michigan for an adult psychiatry residency and concurrently completed a psychodynamic psychotherapy fellowship at the Michigan Psychoanalytic Institute. Following his residency, Dr. Eappen trained at the Institute of Psychiatry at the Medical University of South Carolina in Charleston, SC for a child psychiatry fellowship, where he served as chief fellow in his final year of training. During residency and fellowship, Dr. Eappen published multiple articles in peer-reviewed psychiatric journals, on topics ranging from pharmacology to child & adolescent forensic psychiatry. His co-authors have included Dr. Elissa Benedek (former president of the American Psychiatric Association) and Dr. Gregory Dalack (chairman of the University of Michigan Department of Psychiatry). During his training, Dr. Eappen recognized the divergence in the quality of psychiatric care from his residency and fellowship programs and the hospitals and clinics he rotated in as a medical student in the Chicagoland area. To narrow this gap in care, he founded the Eappen Clinic. Since founding the Eappen Clinic in 2016, Dr. Eappen has become nationally recognized for his expertise in psychiatry and healthcare, having been interviewed by publications including The Wall Street Journal and Cosmopolitan. He was also featured in the University of Michigan Department of Psychiatry’s 2024 Alumni Spotlight.

Dr. Eappen