Medication-induced movement disorders

Medication Induced Movement Disorders 897
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Medication-induced movement disorder occurs due to treatment with antipsychotic medications. Most medication-induced movement disorders are caused by medications that block the action of dopamine, a neurotransmitter that allows communication between two neurons to take place and that is necessary for coordination of movements of different parts of the body. When the receptor where dopamine is supposed to bind is blocked, certain movement-related side effects occur. All of the medications that block dopamine receptors are called neuroleptics.

Neuroleptics include both conventional or typical antipsychotic agents, such as chlorpromazine (Thorazine), haloperidol (Haldol), and fluphenazine (Prolixin), as well as the newer, or atypical, antipsychotic agents such as clozapine (Clozaril), risperidone (Risperdal), olanzapine (Zyprexa), and quetiapine (Seroquel). In general, the newer, atypical antipsychotics appear to have a lower likelihood to cause movement disorders than the older, typical medications. Other neuroleptics include certain drugs used in the treatment of physical symptoms such as nausea, and include prochlorperazine, promethazine, and metoclopramide, as well as amoxapine (Asendin), which is marketed as an antidepressant.

There are other medications, however, that do not block dopamine action but still cause movement disorders. They are not referred to as neuroleptics, and they include lithium carbonate , valproic acid and a class of drugs called selective serotonin reuptake inhibitors (SSRIs). The disorder caused by these medications is called medication-induced postural tremor.

All of the disorders caused by neuroleptics, which include antipsychotics and other medications that block dopamine, as well as disorders caused by non-neuroleptic medications, are collectively referred to as medication-induced movement disorders.



Medication-induced movement disorders caused by neuroleptics are divided into three time periods. The early-onset type, which usually occurs within the first seven days of treatment with neuroleptics, is known as neuroleptic-induced acute dystonia. Neuroleptic-induced acute dystonia is characterized by abnormal contractions of various muscle groups resulting in spasm and/or twisting of the head, neck, jaw, lips, tongue, and eye muscles as well as abnormal movements and postures of the limbs and the trunk.

The intermediate-onset types of movement disorders associated with the use of neuroleptics usually develop within the first three months of treatment. They are known as neuroleptic-induced Parkinsonism and neurolepticinduced akathisia. Neuroleptic-induced Parkinsonism is associated with difficulty initiating movements. Once movements are initiated, they are very slow. Other characteristics of neuroleptic-induced Parkinsonism are tremor and rigidity in muscles. Neuroleptic-induced akathisia is associated with uncontrollable restlessness that may involve compulsive foot tapping, pacing, and a sense of inner tension.

The late-onset type of neuroleptic-related movement disorder is known as neuroleptic-induced tardive dyskinesia and the onset is usually seen many months to years after starting the neuroleptic treatment. Neurolepticinduced tardive dyskinesia involves grotesque, repetitive, and involuntary movements. They are usually seen in the mouth and face.

A movement disorder that can occur at any time during the course of neuroleptic treatment is known as neuroleptic malignant syndrome. It is a serious condition and is characterized by changes in consciousness, ranging from agitation to coma. The patient may experience high fever, and increases in blood pressure and heart rate, as well as severe muscular rigidity.


All of the movement disorders mentioned above are related to the use of neuroleptic medications. However, other drugs, such as lithium, valproic acid, isoproterenol, amphetamine, theophylline, as well as a class of drugs known as tricyclic antidepressants, may also cause a movement disorder that is mainly characterized by postural tremor, a rhythmic alteration in movement. Lithium-induced tremor may take the form of twitching in the arms and legs.

Causes and symptoms


Neuroleptic-induced movement disorders are caused because the actions of dopamine are blocked. Dopamine is a neurotransmitter necessary for coordination of movements of different parts of the body.

Other medications, which are not classified as neuroleptics, block the action of other neurotransmitters as well as dopamine. However, because they essentially block the action of dopamine, they cause similar unwanted effects associated with movements.


Neuroleptic-induced acute dystonia is associated with primarily abnormal postures and muscular spasms. They are usually characterized by abnormal positioning of the head and neck in relation to the body, spasms of the jaw muscles, impaired swallowing, speaking or breathing, thickened or slurred speech due to a slow movement of the tongue, tongue protrusion or tongue dysfunction, eyes deviated up, down, or sideways, and abnormal positioning of the limbs or trunk. Patients experience pain and cramps in the affected muscles. In addition, many patients experiencing dystonia due to the neuroleptic treatment also experience fear and anxiety. This is especially present in patients who are not aware of the possibility of developing dystonia and who mistakenly associate these side effects as part of their mental illness.

Neuroleptic-induced Parkinsonism includes rigidity, tremor, and bradykinesia (slow movements). The tremor is a rhythmic, three- to six-cycle-per-second motion that is present at rest. The tremor can affect the limbs, head, mouth, or lips. Rigidity signifies the degree of tension present in the muscle. It can be either continuous or intermittent in the affected limbs or joints. Bradykinesia includes decreased arm movements related to walking, as well as difficulty initiating movement. Drooling may occur due to a decrease in pharyngeal motor activity. People experiencing neuroleptic-induced akathisia usually feel anxious, agitated, and unable to relax. They also may pace, rock while sitting and standing, and often rapidly alternate between sitting and standing.

Neuroleptic-induced tardive dyskinesia manifests itself in involuntary movements of the tongue, jaw, trunk, or extremities. It occurs most commonly in patients who have taken older antipsychotic medications for many years, although the condition may appear earlier than that (after one year of treatment with neuroleptics, or even earlier than that, especially in elderly people). The movements can be rapid and jerky, slow and continual, or rhythmic in nature. Over three-fourths of the individuals with neuroleptic-induced tardive dyskinesia have abnormal movements of the face and the mouth. This may include licking, sucking or smacking of the lips, chewing movements, jaw deviations, grimacing, grunting and other peculiar sounds, or brow furrowing. About one-half of patients with tardive dyskinesia have abnormal limb movements, while about one-quarter have disposition of the trunk.

The basic features of neuroleptic malignant syndrome is the development of high fever and severe muscle rigidity. These can be accompanied by tremor, changes in level of consciousness ranging from confusion to coma, increased heart rate and blood pressure. The fever can be mildly elevated (99–100°F) or severe (106°F). Neuroleptic malignant syndrome can be fatal in some cases, while it is relatively benign in others. There are no known predictors of neuroleptic malignant syndrome. However, it usually develops four weeks after starting neuroleptics, and about two-thirds of cases develop within the first week of treatment. A very small number of patients develop neuroleptic malignant syndrome many months after taking the neuroleptic.

Medication-induced postural tremor is characterized by a regular, rhythmic oscillation of hands and fingers, head, mouth, or tongue. The frequency of the tremor ranges from eight to 12 cycles per second. These are most easily observed when the affected part is in a sustained position (for example if hands are outstretched or the mouth is held open).


Neuroleptic-induced acute dystonia occurs most commonly in young males. It is far less likely to occur with the newer medications known as atypical neuroleptic medications, such as clozapine, risperidone, olanzapine, and quetiapine. The possibility of neurolepticinduced acute dystonia occurring with these atypical medications is less than 5%. The possibility of this side effect occurring with the conventional or typical neuroleptics is about 15-20%. The incidence is inversely correlated with age, meaning that younger persons are more likely to experience dystonia.

Neuroleptic-induced Parkinsonism is directly correlated with age. This means that older patients are more likely to experience this effect. It occurs in about 30% of patients. Neuroleptic-induced acute akathisia is not related to age and occurs in about 20% of patients being treated with neuroleptics.

The incidence of neuroleptic-induced tardive dyskinesia is related to total lifetime of treatment with antipsychotics. The cumulative incidence is about 5% per year of therapy. This essentially means that there is a 50% chance of developing tardive dyskinesia with 10 years of treatment with neuroleptics.

The incidence of neuroleptic malignant syndrome is about 0.5%. This condition is fatal in about 20 to 30% of cases.

Most available information on medication-induced postural tremor is about lithium-induced tremor. The prevalence of this condition is about 40%.


People taking antipsychotic medications and other medications that block dopamine action must be regularly evaluated by a physician to monitor for medicationinduced movement disorders. In order for these conditions to be officially diagnosed, certain criteria must be met.

Neuroleptic-induced acute dystonia must have one or more of the following developed in association with the use of neuroleptic: abnormal positioning of the head and neck in relation to the body, spasms of the jaw muscles, impaired swallowing, thickened or slurred speech, tongue protrusion or dysfunction, eyes deviated up, down, or sideways, or abnormal positioning of limbs or trunk. These symptoms need to have developed within seven days of starting the neuroleptic medication. Moreover, the symptoms cannot be associated with an underlying mental disorder, and they can't be due to a medication other than a neuroleptic. Dystonia due to neuroleptics needs to be distinguished from dystonia due to neuroleptic malignant syndrome.

Neuroleptic-induced Parkinsonism needs to have the triad of symptoms described above which include tremor, rigidity, and bradykinesia (slow movements). These symptoms cannot be related to a non-neuroleptic medication, or a psychiatric condition, such as Parkinson's disease, Wilson's disease, neuroleptic malignant syndrome, or substance withdrawal. Neuroleptic-induced akathisia is due to the use of a neuroleptic and not to anxiety, substance withdrawal or psychotic agitation. At least one of the symptoms of fidgety movements or swinging the legs, rocking from foot to foot while standing, pacing to relieve restlessness, or inability to sit and stand needs to be present. These symptoms must have developed within four weeks of initiating the therapy with neuroleptics.

Neuroleptic-induced tardive dyskinesia needs to include involuntary movements over a period of at least four weeks that manifest themselves as rapid and jerky, slow and continual, or rhythmic movements. The exposure to neuroleptics needs to be for at least three months, and the symptoms cannot be due to a neurologic condition, such as Huntington's disease, Wilson's disease, Sydenham's (rheumatic) chorea, systemic lupus, or hyperthyroidism.

Neuroleptic malignant syndrome must include severe muscle rigidity and elevated temperature as well as at least two of the following symptoms: sweating, difficulty swallowing, tremor, incontinence, changes in level of consciousness, mutism, increased heart rate, elevated blood pressure, or laboratory evidence of muscle injury. These symptoms cannot be due to another substance or a medical condition, such as viral encephalitis, or mood disorder with catatonic features.

The criteria for diagnosing medication-induced postural tremor includes a development of tremor associated with the use of a medication other than a neuroleptic. The tremor cannot be due to a non-medication condition that was present prior to starting the medication and cannot continue to be present following discontinuation of the medication. These criteria are helpful in distinguishing the tremor due to medication use from the tremor due to anxiety, alcohol withdrawal, stress , or fatigue . The tremor must have a frequency between eight and 12 cycles per second, and the tremor must not be caused by neuroleptic-induced Parkinsonism.


In an attempt to prevent acute dystonia from developing, physicians may prescribe a preventative medication along with the antipsychotic (see "Prevention," below). Once neuroleptic-induced acute dystonia has appeared, however, there are several treatment options. A medication called benztropine in doses ranging from 1 mg to 8 mg is effective in reducing symptoms associated with dystonia. Most patients take 2 mg twice daily for seven days for prevention of dystonia at the time they are starting neuroleptic treatment. When benztropine therapy is initiated, the dose is slowly increased. Moreover, when discontinuing the treatment with benztropine, the dose should be slowly decreased to prevent the nausea and vomiting associated with abrupt withdrawal. Another medication that may be useful in treating neurolepticinduced acute dystonia is called trihexyphenidyl . The doses can vary from 10 mg to 45 mg daily. Younger patients may respond better to the treatment with trihexyphenidyl because they can tolerate higher doses. The third pharmacological option is diphenhydramine (Benadryl). This medication can be taken for the period dystonic symptoms last. Another option may include switching the patient to one of the newer antipsychotics, such as clozapine, risperidone, or olanzapine, since each of these has a low incidence of causing dystonia.

There are a couple of ways to treat intermediate-onset movement disorders due to neuroleptics. Amantadine is a medication that is approved by the United States Food and Drug Administration for the treatment of Parkinsonian symptoms. Another helpful medication called propranolol comes from a class of drugs called beta blockers . Propranolol has been reported effective in the treatment of akathisia. The doses that are effective range from 20 mg to 100 mg daily. The response to propranolol is usually seen within the 24 hours of administration. Switching the patient to a newer or atypical antipsychotic, such as clozapine, or decreasing the dose of the current antipsychotic sometimes helps the condition.

There are no effective treatments for tardive dyskinesia once it develops. Tardive dyskinesia is associated and strongly correlated with the cumulative dose of the antipsychotic during years of treatment. Hence, the key to tardive dyskinesia is prevention. If possible, a newer medication, such as clozapine or risperidone, which have only a few case reports of tardive dyskinesia, should be used whenever possible. In many cases, if tardive dyskinesia is noticed early in a regular check-up with the physician, and if the medication causing the condition is stopped, the symptoms of tardive dyskinesia will subside. If the symptoms continue after the antipsychotic has been discontinued, the situation becomes difficult. Treatment will most likely involve movement disorder specialists and may or may not be successful. The medications reserpine and levodopa may be helpful for some patients.

The most common medications used to treat neuroleptic malignant syndrome are dantrolene, (a muscle relaxant that helps with the fever), bromocriptine, and amantadine.

In order to reduce medication-induced postural tremor, the lowest possible dose of the psychiatric drug should be used. Moreover, a medication from the beta blockers, such as propranolol, can be used to help with the symptoms.


The prognoses for the early- and intermediate-onset of movement disorders are very good, especially with the option of switching the patient to a newer antipsychotic such as clozapine.

The prognosis for the late-onset disorder called tardive dyskinesia is very poor. Once the condition occurs, it is essentially irreversible and is very difficult to treat.

Neuroleptic malignant syndrome is a serious condition. It is deadly in about 20 to 30% of patients. Those who survive have a good chance of recovering.

Medication-induced postural tremor is very well-controlled with propranolol, and hence the prognosis is good while the patient is being treated with the medication causing the movement disorder.


To prevent acute dystonia, some physicians prescribe benztropine, diphenhydramine, or other medications that treat dystonia, at the outset of treatment with an older antipsychotic.

The most important component of neurolepticinduced tardive dyskinesia is prevention. If conventional antipsychotics are used, the drug use, drug dose, and the duration of use therefore should be minimized.

In order to avoid medication-induced postural tremor, patients should limit the amount of caffeine consumption. Also, in order to minimize the amount of daytime tremor they should take the psychiatric drug at bedtime.



American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 4th edition, text revised. Washington, DC: American Psychiatric Association,2000.

Gilman, Alfred G. The Pharmacological Basis of Therapeutics. McGraw-Hill, 1996.

Kaplan, Harold. Comprehensive Textbook of Psychiatry. Williams and Wilkins, 1995.

Lacy, Charles F. Drug Information Handbook. Lexi-Comp, Inc. 2002.


Heaton, Robert. "Stability and Course of Neuropsychological Deficits in Schizophrenia." Archives of General Psychiatry 58 (2001): 24–32.

Littrell, Kimberly. "Marked Reduction of Tardive Dyskinesia With Olanzapine." Archives of General Psychiatry. 55(1998): 398–403.


American Psychiatric Association. 1400 K Street NW, Washington D.C. 20005. <> .

American Thyroid Association. 6066 Leesburg Pike, Suite 650, Falls Church, VA 22041. <> .

Canadian Movement Disorder Group, affiliate of Canadian Congress of Neurological Sciences. 709 7015 Macleod Trail SW, Calgary, AB T2H 2K6 Canada. <> .

We Move, worldwide education and awareness of movement disorders. 204 West 84th St., New York, NY 10024. <> .

Ajna Hamidovic, Pharm.D.

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cathy christensen
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Nov 13, 2007 @ 1:01 am
I am in a very scarey and difficult situation. I took Risperdol for three years, ans Zyprexa for 5 years before that. A year ago I developed Parkinsonian sympyoms to the point where I could only walk with crutches. My internist referred me to a neurologist who did a COMPLETE workup...his opinion was Risperdol induced Parkinsinism and he recommended 100 mg Amnantadine daily, and of course discontinue the use of Risperdol. My internist recommended a second opinion from a Board Certified psychiatrist/neurologist. He only did a neurological work-up and recommended to my psychiatrist that I take Seroquil. I took it for 2 weeks and my symptoms got worse so I stopped it. I saw him 2 weeks later and he put me on Pexeva... the same as Paxil only the foundation is a different salt. At that point I was off the crutches and functioning normally. The Pexeva worked EXTREMELY WELL for my paranoia,anxiety, and depression.
HOWEVER, within 3 months I began experiencing even WORSE Parkinsonian symptoms, to the point where I could not predict when I would totally slurr my words or freeze up and fall down when trying to cross the street.Every health care practioner I spoke with told me Paroxitine (Paxik...Pexeva would never cause these sympyoms). I phoned the Pexeva company and was on the phone with them for 2 hours... finally their health care specialist found in small print on the 9th page of their disclosure that pretrials had shown a miniscule number of persons had shown extra pyramidial symptoms... Parkinsonism. That was 2 weeks ago.. today is Nov. 12th. The Paroxitine is wearing off and I am beginning to experience paranoia, hallucinatioms, anxiety, and severe depression.
I was a licensed therapist in California for 20 years.
I can't find ANYBODY who will understand this situation and prescribe me the appropriate medication.
This is my situation as of tonight.
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Oct 14, 2011 @ 10:10 am
I was diagnosed 3 years ago with Medication-Induced Postural Tremor due to taking Depakote for 25 years at dosages from 500 mg. up to 3000 mg. I was sent to a neurologist who diagnosed me with Parkinson's Disease. I have been taking sinemet in varying dosages since then. I am now taking Sinemet 50/200 ER every three hours along with two Lodosyn every 8 hours. I have noticed that after about 2 hours after taking a dose I feel very weak and sort of out of it. Then at the 4 to 6 hour mark my Parkinson's symptoms increase alot. I have hand tremors and the other movement probklems associated with Parkinson's. Then at the 8 hour mark after the dose has worn off I feel better, no tremors or movement problems. I shared this with my neurologist who was not able to come up with a reason for this. He consulted with another neurologist who said maybe it was because I wasn't always eating breakfast. I have been eating cereal with milk 1/2 hour after my first morning sinemet dose. However, there are times when I don't eat breakfast and neither situation seems to change the 2 hour and 4 to 6 hour symptoms. I feel that I may have medication-induced postural tremor and I would like to pursue the possibility. If in fact this is what I have should I be taking sinemet at all. The neurologist does not seem to even entertain this disagnosis. I would like to consider it and be treated for medication-induced postural tremor to see if I improve. If I do have this would the sinemet actually be increasing my symptoms. What do you suggest? Should I get a second opinion if my neurologist refuses to try treating me for medication-induced postural tremor. Would it hurt to try treatment for this to see if in fact it helps or since I've been on sinemet is this out of the quesiton.

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