The Good, the Bad, and the Ugly: An Infographic on Bipolar Drugs

Craig Wagner

This post helps make sense of the mountain of bipolar drug research. It distills into an infographic the pros and cons of five classes of bipolar drugs and gives observations on what it means for people who face choices on bipolar care.

Although this post wanders deeply into the statistical weeds, we avoid technical jargon. To maintain statistical rigor, we use technical definitions for important phrases below. [1]

(The infographic is kept fresh as research evolves. The latest version with footnotes is always here.)

A few key perspectives behind this infographic deserve attention:

How well do bipolar drugs work?

One sentence summarizes scores of bipolar drug studies:

Bipolar drugs work, but 75-85% of the time people don’t see substantial improvement attributable to them. [2]

Let me explain.

To test drugs, researchers take two groups of people with bipolar and give one a drug and the other sugar pills (placebo). After 1-2 months they count how many people in each group see substantial improvement (> 50% symptom reduction). If the tests reliably show more in the drug group, the drug works.

But we need to know much more if we are to make evidence-informed choices of care. We need to know the odds they’ll work. In fact, these odds (called attributable benefit) are vital, since they are the best way to understand the true value of drugs.

Consider lithium for mania. Many bipolar studies show us that we have a 31% chance of substantial mania relief in 1-2 months without using drugs. [3] For reasons we don’t fully understand, our natural healing ability — the placebo effect — works. If you want to boost your odds by 16%, you can take lithium. You will then have a 47% chance of substantial mania relief in 1-2 months (31% attributable to the placebo effect and 16% attributable to lithium). [4]

For bipolar depression, the placebo effect is even more powerful. 39% of people see substantial improvement in 1-2 months without drugs. [5] Taking an antipsychotic (lurasidone) boosts your odds to 59% (39% attributable to the placebo effect and 20% attributable to lurasidone). [6]

Surprisingly, our natural healing ability is twice as powerful as our best gold standard drugs — 1.9X for mania (31%/16%) and 1.95X for depression (39%/20%).

But there is no free lunch. The boost in odds of benefit comes with a boost in odds of harm. Data on harms is poorly quantified and numbers are highly variable, but here are rough odds of experiencing side effects from bipolar drugs: [7]

  • Lithium. Weight gain (75%), tremors (42%), sexual dysfunction (37%), chronic kidney disease (33%), hypothyroidism (14%).
  • Anticonvulsants. Elevated liver enzymes (11%), tremors (10%), rash (10%).
  • Antipsychotics. Weight gain (90%+), sexual dysfunction (66%), fatigue (35%), tremors (17%).
  • Benzodiazepines. Fatigue (50%), sexual dysfunction (33%), withdrawal syndrome (30%).
  • Antidepressants. Sexual dysfunction (58%), withdrawal difficulties (56%), fatigue (21%), weight gain (15%).

Bipolar drug therapy is a balancing act of benefits vs. harms. Odds of attributable benefit cluster in a 15-25% band, so 75%-85% don’t see substantial benefit. Stated differently, if five people take a bipolar drug, only one is likely to see substantial improvement due to it, but all five will have side effects. Experiencing this trade-off firsthand is a major reason why up to 60% of people with bipolar don’t take their medication as prescribed. [8]

Polypharmacy Risk

Most people with bipolar take 2-5 psychiatric drugs (polypharmacy), [9] a practice that boosts symptom relief somewhat, but at considerable additional risk.

Unfortunately, the sheer number of individual bipolar drugs makes drug combination testing “practically nonexistent.” [10] This creates an uncomfortable reality: although psychiatry seeks evidence-based care, it “ventures beyond the evidentiary base” [11] for all but the simplest bipolar prescribing. And straying from the evidence creates grim results: longer hospital stays, [12] increased suicide, [13] and a rise in drug-related illness.

Even if we are comfortable with this added risk, the benefits come with diminishing return. The benefit of multiple drugs is nearly always less than the sum of the parts, and in some cases add-on drugs provide no benefit at all (as we will see with antidepressants).

Antipsychotic polypharmacy — taking two or more antipsychotics at once — is considered one of the riskiest forms of polypharmacy. In fact, the American Psychiatric Association (APA) launched a campaign targeting antipsychotic over-use. The APA’s CEO and Medical Director cautioned, “…Physicians and patients together should be thinking carefully. Are the medications really needed and are there downsides and negative consequences for overuse?” [14]

This caution is well-placed: those on two or more antipsychotics for bipolar have almost triple the risk of requiring medical care, with no improvement in functioning. [15] And the greater the number of antipsychotics taken concurrently, the shorter the expected life span. [16] Despite this evidence, 10% of people with bipolar are on two or more antipsychotics.

Evidence on antidepressants

The largest-ever federally funded trial for bipolar depression reached a startling conclusion: antidepressants don’t work (don’t outperform placebo) when added to mood stabilizers (lithium or anticonvulsants). [17] And most people taking bipolar drugs are on mood stabilizers. [18] It also found that those on antidepressants were less likely to achieve durable recovery. [19]

Gold-standard meta-analyses and systematic reviews in 2001, 2008, 2011, 2012, 2013, 2014, and 2016 all reached variations of the same conclusion: antidepressants don’t work for bipolar. [20] One meta-analysis concluded: “evidence of efficacy does not support the short-term or long-term application of antidepressant therapy in patients with bipolar.” [21] Another warns that the research “suggests an unfavorable risk / benefit relationship for long-term antidepressant treatment in bipolar disorder.” [22]

This scientific reality collides with a prescribing reality: 30-81% of people treated for bipolar depression are taking antidepressants. [23] This disconnect is the largest controversy in bipolar care. To resolve it, a global expert task force of researchers and clinicians was convened in 2013. After considering all the studies, they found there was insufficient evidence to make any broad statements supporting antidepressants. [24]

Bottom line: antidepressant prescribing for bipolar is extremely common, but gold-standard studies and expert consensus offer scant support.

How does this happen?

First, bipolar prescribing guidelines — the rules that tell doctors what to prescribe in what situations — are inconsistent and some recommend antidepressants beyond the evidence. [25] Japanese guidelines conclude that bipolar is resistant to antidepressants. They don’t recommend them. Australia, New Zealand, and the U.K. updated their guidelines to reflect a more cautious view of antidepressants, not recommending them, but providing guidance should they be prescribed. Guidelines in Canada hold as a basic principle to discontinue antidepressants in many cases but consider them a possible second-line treatment. APA guidelines were last updated in 2005 and have not been changed to reflect global consensus opinion or recent research. They recommend first-line adjunctive antidepressant use and — remarkably — using two antidepressants at once. APA guidelines require urgent updates.

Second is the strong tendency to limit therapy to the five bipolar drugs. When initial drugs aren’t effective, antidepressants may appear “inevitable” [26] — a seemingly prudent leave-no-stone-unturned last resort. But limiting recovery options isn’t a good idea. Dr. Kenneth Duckworth, Medical Director of the National Alliance on Mental Illness emphasizes, “Psychiatric medications are rarely enough to promote recovery alone.… Use of non-medication strategies is crucial for most clinical situations…” [27]

Third is antidepressant withdrawal difficulties. It’s easy to get on antidepressants, but often hard to get off. 56% of people experience antidepressant withdrawal, 46% of these find it severe. [28] Many people can feel stuck — unable to extricate themselves from a potentially poor risk/benefit trade-off.

Although experts express no broad support for antidepressants, are there narrower bipolar situations where they are clear winners? Unlikely. Diligent research hasn’t found them.

Stand-alone antidepressants aren’t recommended nor FDA-approved since they can promote mania and switching. [29] Add-on antidepressants to mood stabilizers provide no benefit. [30] One antidepressant (fluoxetine) helps depression when combined with an antipsychotic (olanzapine), but the solution is almost as likely to harm as help. [31] Short-term use for bipolar II may provide value, but it can easily slide to long-term use because of antidepressant withdrawal difficulties. Long-term use may reduce the risk of new depression but it increases mood fluctuations [32] and the lifetime risk of polarity change and mixed episodes. [33]

Over 4 million people in the U.S. and U.K. are being prescribed antidepressants for bipolar when expert consensus and gold standard analysis confirm that the supporting evidence is weak and there is no corner of bipolar where antidepressants are shown to provide a compelling and reliable cost/benefit trade-off.

Nondrug options work

But there is good news. A paradigm shift is underway from conventional psychiatry to Integrative Mental Health, a discipline that includes the best of drug and nondrug therapies. Thankfully, options beyond the five bipolar drugs work. And we define work in the same way researchers do for drugs: they outperform placebo in randomized controlled trials.

Omega-3 fatty acids, [34] light therapy, [35] and folic acid (added to lithium), [36] can improve bipolar depression. Amino acid supplements appear to reduce mania. [37] Probiotics can reduce bipolar rehospitalization. [38] Cognitive Behavioral Therapy works on many levels, decreasing relapse rates, depression, and mania while improving psychosocial functioning. [39] One randomized controlled trial found that treating underlying inflammation — a common denominator in mental distress — with simple aspirin provided an attributable benefit for bipolar depression on par with psychiatric drugs [40].

These are not guaranteed solutions nor extensively tested. But neither are the multi-drug combinations commonly prescribed for bipolar.

But unlike drugs, nondrug options typically come with no or mild side effects and often support sustainable wellness. Additionally, some options address causative factors of bipolar distress, going well beyond the symptom management of bipolar drugs. For example, detailed blood tests help identify specific nutrient, gut-health, hormonal, and immune system issues that may be influential. This is important since 25% of people have identifiable physical issues that cause or exacerbate their mental distress. [41]

Psychiatrists, therapists, GPs, and other practitioners are advancing this paradigm shift. In fact, the APA sponsors a growing caucus of psychiatrists focused on Complementary and Integrative Medicine, and caucus leaders have recently published a book on evidence-based nondrug options. [42]

Final Thoughts

I leave you with these perspectives:

Drugs aren’t the savior nor the enemy. Blur your eyes and look at the infographic. An expanse of red will wash over your retinas. But there are also swaths of green. Yes, not a lot of big numbers on the green, but green. Many people confirm that drugs help them reside more often in a place of safety and stability from which they can build their recovery. Unfortunately, 75-85% of the time, people don’t see substantial improvement due to a bipolar drug they take. There is far more to healing than can be included in the chemistry of a pill.

Don’t wait for the paradigm shift. Most psychiatrists focus their practice on drug therapy, so you often need to expand your practitioner team to explore nondrug options. Fortunately, there is a vanguard of mental health practitioners that can help. Some are aligned with the emerging evidence of bio-individuality that informs individualized nutrient therapy, shown broadly effective in open label trials. Others see the correlation between bipolar and childhood trauma and are helping address sources of enduring pain. Others are aligned with expert consensus and are creating de-prescribing plans that slowly ween people off psychiatric drugs when needed. And professionals in peer support, mindfulness, mind-body disciplines, and more are providing valuable recovery support.

Nondrug options aren’t a panacea. Although there is growing gold-standard evidence that supports them, it’s much smaller than for drugs. Nondrug options may take longer to show benefit, they require greater personal commitment, most aren’t covered by insurance, and practitioners are scarce. They aren’t miracles. However, their ability to address causative factors of distress, support core wellness, and minimize exposure to the risks and side effects of bipolar drugs make them essential and a pragmatic source of hope.

Build a better plan with your practitioners. Carefully evaluate the evidence on your current bipolar drugs. Understand the odds and answer the APA’s question, “Are the medications really needed and are there downsides and negative consequences for overuse?” If you make adjustments, do so slowly under practitioner care. But — and this is my central point — don’t limit yourself to bipolar drugs. Explore evidence-based nondrug options. Avoid drug myopia. Trust your own experience. Your recovery may well depend on it.

Get started. Review the nondrug approaches most-promising for bipolar. Watch a short video of William Walsh, PhD on the methods and results of Nutrient Therapy for bipolar. Engage a practitioner trained in the diagnosis and treatment of the biomedical issues of mental health (see biomedical practitioner finder). Check out Safe Harbor’s Free Mental Health Strategies — 80 budget-minded nondrug mental health options. Practitioners can obtain Psychiatry Redefined training from Dr. James Greenblatt, one of the country’s leading integrative psychiatrists. Or consider the 27 broad evidence-based nondrug options that span all diagnoses. There is far more available than most people realize.

The only guarantee. Failing to look beyond drugs limits your paths to recovery.


Pause for a moment. Trust yourself. You can do this, and you are worth the effort. Start small. Take one step at a time. Stay close to those who love and support you. Mistakes will be made, and that’s OK. Make the best choices you can as you walk the often-crooked path back home. Others have recovered. So can you.


Epilog: This post leverages our growing library of Integrative Mental Health infographics and resources at Onward Mental Health. If you find them helpful, please use them. We welcome ideas on improvement and expansion. Many thanks to Stephanie Heit for her review and Dan Stradford, President of Safe Harbor, for providing the free mental health strategies. See disclaimer.


See the infographic footnotes and blog post footnotes. Both contain extensive commentary.


  1. Almost forgot my favorite part about ‘dual diagnosis’ its pretty well known that more then 80% of people that come in for drinking or addiction relaps so they fill them up with psychiatric drugs to drink and use on top of when they relapse and get even more erratic then they were before.

    Here is your Zolft Abilify Gabapentin… Don’t drink with this. Ya sure. Half of them drink at the airport on the way home.

    • This makes zero sense to me how the do this, too.

      This is how I believe the Rehab doctors helped kill my best friend, and how some these “accidental” deaths are happening. Putting a newly recovering person on psychiatric drugs that aren’t supposed to be mixed..the person is new to recovery and they are hooked on a psych med that isn’t supposed to be mixed with illicit drugs/ alcohol…but they are off the wagon and do mix..recipe for disaster. Then it gets blamed on accidental OD or suicide. It’s maddening :/

  2. I totally disagree the principle of having a “balanced” point of view on psychiatric drugs. These drugs already benefit from an apologetic publicity from the pharmaceutical industry and the psychiatric staff: to really balance the discussion, only the critic must be put forward: the glorification, we already have ad nauseam.

    On the other hand, the arguments in favor of drugs are extremely doubtful. You did well to present your sources, it makes a difference with the practices of the psychiatric vulgarization.

    Here I will take just one example: you say that lithium could probably reduce the risk of suicide by 14%. However, the study cited (Song J et al, 2017) simply shows that the rate of suicidal events is lower during periods of lithium consumption than during periods of non-consumption, in people who regularly take lithium and subjected to massive psychiatric polytoxicomania (see Table 1 of the original study).

    This is not a proof that lithium reduces the risk of suicidal events. This could be due to withdrawal syndrome, and more so to the consumption of antidepressants that were taken by 70.8% of subjects on lithium. Since lithium reduces mania, while antidepressants increase it, the combination of lithium withdrawal and the use of antidepressants increases the risk of mania, and therefore could increase the risk of suicide events.

    By the way, “At least one suicide-related event during follow-up”

    Lithium: 10.1%
    Valproate: 13.1%
    Never Treated With Lithium or Valproate: 7.8%

    This is statistically significant. From this study, I could possibly conclude that lithium and valproate increase the risk of suicidal events, and that the increase in suicidal events in the lithium group at discontinuation was due to withdrawal syndrome and to the consumption of antidepressants.

    But that would be a hasty conclusion, because all subjects massively consumed all kinds of drugs: the difference in the rate of suicidal events could be due to these drugs or their withdrawal, or to a subtle and complex combination of all this bazaar.

    Moreover, the 8-year actual suicide rates in the lithium (1.1%), Valproate (1.2%) and Never Treated With Lithium or Valproate (1.2%) groups are about the same, and the difference is not statistically significant.

    In any case, this study does not prove that lithium decreases the suicidal risk.

  3. Craig this is just brilliant and genius. I really wish this had been out when I started working in the MH system.
    This is also great for those that I know who have chosen to take chemicals. I would tell them read this read that but this is clarity for visual learning.
    And Cat – I so appreciate your 12 step viewpoint. The old timers were anti – drug and yes they were right.
    The big Pharma folks created moral injury to us all.

  4. My problem with these drug studies and when claims are made that there is a “reduction in symptoms” (whatever that might mean) is how do they account for the myriad of factors that could have contributed to doing or feeling better in addition to ingesting the drug. It is as if we are seen as an inert recipients of “treatment” and that nothing else goes on for us or in our lives while we just wait for the drugs to do their magic

  5. This info graphic should be handed to all patients and their families if they are “diagnosed” with so-called “bipolar disorder”.
    ADHD drugs and anti-depressants trigger symptoms of “bipolar” in many people.
    Poisoning ppl bc of ignorance and $.