Disclaimer: Nothing on this site is meant to be construed as medical advice. Any information on this site is the opinion of the author. You should discuss treatment options with your doctor. By reading this site you are agreeing that www.tourettestreatment.com is not liable for any medical decisions you make.

 

What follows are my notes that I took while researching treatment options for tic disorders. Some fields are black because I was either unable to find the correct information, or because they are irrelevant. Medications are groups according to class (neuroleptic, SSRI, etc.) Where applicable, notes about the entire class of medication have been added beneath the class name. For each class of medication, information is divided into the following sections:

 

Name - name of the medication

Tradename - tradename of the medication

Method - the method of action, or how the medication works

Notes - notes I found about the medication or results from trials

Side-effects - documented side-effects for the medication

 

All medications listed below were found somewhere in medical journal(s) with reference to the treatment of Tourette's Syndrome and/or tic disorders.

 

Studies and references are cited where I still have the reference, but since this information comes from casual notes that I took while reading various source, I don't always have the reference information available. I will make an attempt to find the sources and post it after the study in the appropriate tables as I update this list.

 

Again, this information represents my collection of notes and is not guaranteed to be accurate or complete. It is not meant to be a diagnostic tool, a recommendation, or any form of advice. This is for informational purposes only. Please do your own research and discuss your own situations with your doctor.

 

 

Anti-psychotics/Neuroleptic

(- All neuroleptic medications may cause tardive dyskinesia, a potentially irreversible movement disorder

- Not to be discontinued abruptly - may cause tardive dyskenesia

- May begin to work in a few days or weeks

- May cause sleepiness, depressed mood, weight gain

- May cause other movement disorders including bradykinesia, akathisia, and acute dystonic reactions

- Antipsychotics may worsen tics - http://www.aafp.org/afp/990415ap/2263.html )

 

Name
Tradename
Method
Notes
Side-effects

Pimozide

Orap

 

Only FDA-approved antipsychotic for the treatment of tics

- Cardiac changes (in the QT interval)- One double-blind study found Pimozide superior to Haloperidol with respect to efficacy and side effects

- muscular rigity, drooling, tremor, lack of facial expression, slow movement, and restlessness

Haloperidol

Haldol

   

- 4% per year risk of tardive dyskinesia in younger patients, higher in those over 45

- depression resulting in suicide is common during long-term treatment

- musular rigity, drooling, tremor, lack of facial expression, slow movement, and restlessness

Fluphenazine

Prolixin

 

- Seemingly less common side effects than other neuroleptics

 

Sulpiride

Not approved in US and Canada

Dopamine blocker

Anti-psychotic

- fewer extrapyramidal side effects than many of the older antipsychotic medications

Thioridazine

-Mellaril

-Novorizadine

-Thioril

   

- Can prolong QT interval (lead to sudden death)

 

 

 

Atypical Neuroleptic

(- All atypical neuroleptic medications may cause tardive dyskinesia, a potentially irreversible movement disorder, although the risk with atypical neuroleptics is thought to be lower than with neuroleptics

- Not to be discontinued abruptly - may cause tardive dyskinesia

- May begin to work in a few days or weeks

- May cause Neuroleptic Malignant Syndrome

- Increased risk of diabetes mellitus and hyperglycemia

- May cause sleepiness, depressed mood, and weight gain

- Atypical antipsychotics share a relatively greater affinity for the 5-HT2 and D2 receptors than traditional antipsychotic agents and cause a lower incidence of extrapyramidal effects (such as tardive dyskinesia - http://www.wipo.int/pctdb/en/wo.jsp?IA=US2002033628&DISPLAY=DESC)

 

Name
Tradename
Method
Notes
Side-effects

Risperidone

Risperdal

 

-Dopamine and serotonin blocking properties

-effective compared to placebo

-at least as effective as Clonidine

-Some reports say it can help OCD, others say it exacerbates symptoms

-Shown to be effective in reducing tic frequency and intensity in most, but not all, studies

- Can prolong QT interval (lead to sudden death)

- Tardive Dyskinesia

Olanzapine

Zyprexa

Dopamine-2 and serotonin-2A and -2C antagonism

- "Some improvement" (Budman, Gayer, Lesser, Qiuhu Shi, Bruun)

- Sedation

- Weight gain

- Increased appetite

- Dry mouth

- Transient asymptomatic hypoglycemia

Thiothixene

Navane

     

Clozapine

Clozaril

 

- Patient developed invluntary movements during treatment with clozapine and fluvoxamine

 

Quetiapine

Seroquel

blocks D1 and D2 receptors, and 5-HT2A, 5-HT2C, 5-HT1A, 5-HT1D, and alpha receptors

Found to decrease tic severity by 35% compared with a 7% change in placebo

 

Ziprasidone

Geodon

 

Found to significantly reduce tic frequency and count over placebo

-Cardiac changes in the QT interval

-Prolonged QT interval can cause ventricular fibrillation and sudden death

-Less likely to cause weight gain

Aripiprazole

Abilify

   

Tardive dyskinesia

 

 

 

SSRI (Selective Serotonin Reuptake Inhibitor)

("When used alone, antidepressant medications are not useful in the treatment of tics" - http://www.coursework4you.co.uk/francis.htm)

(McDougle et al. found that "compared to patients with OCD but no tics, patients with tic-related OCD showed less theraputic response to monotherapy with an SSRI)

Name
Tradename
Method
Notes
Side-effects

Sertraline

Zoloft

   

- Movement disorder side-effects (Lambtert, Trutia, Petty)

Fluoxetine

     

- Movement disorder side-effects (Lambtert, Trutia, Petty)

- Exacerbate tics in a patient with TS but was found to have no effect on tics in a small, double blind, placebo-controlled crossover trial

Paroxetine

     

- Movement disorder side-effects (Lambtert, Trutia, Petty)

- One case of Paroxetine worsening tics in a 12 year old boy with TS

Fluvoxamine

Luvox

 

- Most often used to treat OCD

- One of few SSRIs to have monocyclic structure

- Improvement in 21% of patients with OCD and chronic tics, 52% response rate in patients with OCD and NO tics (source )

- Normal SSRI side effects

- Single case of this drug causing TS in a patient being treated for OCD (source)

- Akathasia, dyskinesia

- Cases of Fluvoxamine worsening tics

Citalopram

Celexa

 

- shows to "significantly reduce tics in TS in one small study"

- No reports to date of this agent exacerbating tic symptoms

- No evidence directly impolicating Citalopram with teeth grinding (bruxism)

 

Escitalopram

   

- Examined in depressed, but not OCD

 

 

 

 

Non-SSRI Antidepressant

Name
Tradename
Method
Notes
Side-effects

Nefazodone

Serzone (Discontinued by Bristol-Myers Squibb in US and Canada in 2004; generic formulations are still available)

Blocks post-synaptic serotonin type-2A receptors and, to a lesser extent, by inhibiting pre-synaptic serotonin and norepinephrine (noradrenaline) reuptake. Also a relatively potent alpha-1 adrenoceptor antagonist

Unlike most SNRIs and SSRIs, Nefazodone has no negative effects on libido or sexual functioning

 

Bupropion

Wellbutrin, Zyban

Norepinephrine and dopamine reuptake inhibitor, and nicotinic antagonist

- found to exacerbate tics in four children with TS

- no reports of it improving tics

 

 

 

 

Tricyclic Antidepressant

(Older than SSRIs, typically more side-effects)

 

Name
Tradename
Method
Notes
Side-effects

Clomipramine

Anafranil

- Strong, but not completely selective serotonin reuptake inhibitor, as the primary active metabolite desmethylclomipramine acts preferably as a norepinephrine reuptake inhibitor

- Alpha blockage, beta receptor downregulation, and postsynaptic antagonism on histamine H1 receptors and dopamine receptors have also been noted

- downregulation of NMDA receptors

Tricyclic antidepressant

- higher incidence of seizures than seen with other tricyclic antidepressants

- No benefit found for Clomipramine or desipramine for patients with TS

- Reported to worsen motor tics in one case with OCD and schizoid personality disorder

Nortriptyline

 

Inhibits reuptake of norepinephrine and to a lesser extent, serotonin

- shown to improve tic symptoms in a chart review of 12 cases of children with tics and ADHD

 

Imipramine

-Antideprin

-Deprenil

-Deprimin

-Deprinol

-Depsonil

-Dynaprin

-Eupramin

-Imipramil

-Irmin

-Janimine

-Melipramin

-Surplix

-Tofranil

-Norepinephrine reuptake inhibition (strong)

- Serotonin reuptake inhibition (moderate to strong)

- Acetylcholine antagonist at M2 muscarinic acetylcholine receptors

- Epinephrine - antagonizes adreno-receptors (II)

- Dopamine reuptake and release at D1 and D2 receptors ("similar to but less potent than the psychostimulants, dopamine agonists and atypical antidepressant buproprion on dopaminergic mechanisms (increase in release and blockage of reuptake inhibition")***

- Opiates and Enkephalinase - low activity

- Histamine antagonist at H1 receptors. Acute sedative effects

(all data in this cell from wikipedia)

- *** says it's similar on dopamine to Buproprion, which has been known to exaverbate tics

- reported to decrease tics in one TS case and have no effect on TS symptoms in another

fever, chills, cough, weight loss, irregular heart rhythms, weight gain (in contrast to weight loss, mentioned earlier), sexual side effects, tremor has been frequently reported, headache, confusion, aggressiveness, weakness, sudden muscle spasms

 

 

 

Blood Pressure medication

Name
Tradename
Method
Notes
Side-effects

Clonidine hydrochloride

Catapres

- Alpha 2-adrenergic agonist

- °62- agonist

-may take time to build up in the system before it begins working

- also used to treat ADHD

- combined with Ritalin reduced the severity of a child's tics with 75% showing improvement

- more effective in reducing motor tics than reducing vocal tics (Nass & Bressman, 2002)

- 11% of patients had significant improvement, 14% had moderate improvement, 67% of subjects had no improvement or worsening

- another study showed no statistical improvements in tic distribution, frequency, or severity

- another placebo controlled double blind study confirmed that Clonidine is effective in lessening tics

-Dry mouth

-Drowsiness

Guanfacine

Tenex

- Alpha 2-adrenergic agonist

- °62- agonist

- a study found a significant decrease in the severity of motor and phonic tics

- double bline study of guanfacine for tics and ADHD found a 31% decrease in tic severity compared to placebo

-Dry mouth

-Drowsiness (less than Clonidine)

 

 

 

Dopamine inhibitors/blockers

Name
Tradename
Method
Notes
Side-effects

Tetrabenazine

Not approved by the FDA as a treatment for tics

 

Approved by FDA for use in US on 8/15/08?

- Blocks dopamine receptors

-Dopamine depleter

-Monoamine - depleting

- Produced significant tic amelioration in over half the patients followed for over two years (Jankovic and Beach, 1997)

- "Powerful anti-tic drug"

- Does not cause tardive dyskinesia

- Given to 5 patients, 2 had good results, 3 had no improvement but experienced side effects

- 57.4% improvement in 47 patients with tics in an open label study (Jankovic and Beach)

-Parkinsonism, sedation, akathisia, depression

 

 

 

Dopamine agonist

Name
Tradename
Method
Notes
Side-effects

Pergolide

withdrawn from US market on 3/30/2007

- on the premise that dopamine agonists in very low dosages preferentially act on the presynaptic receptors and thereby decrease dopamine release…

- success on a trial group that was unresponsive to neuroleptics suggests that in these patients the improvement due to pergolide is not linked to an effect on D2-receptors-carrying GABAergic neurons, as usually assumed, because the patients did not respond to neuroleptics acting in this way. In these 3 cases, unlike in other TD patents, a prevalent action of pergolide by pre-synaptic inhibition of dopamine release on D1-receptors-carrying GABAergic neurons is suggested. (source)

- In an open-label study of 32 patients, there was a 50% reduction in tics in 24 patients.

- In a randomized double-blind placebo-controlled crossover study with 24 subjects, 19 completed. Statistically significant reductions with few side effects

- this is an older Parkinson’s drug

- in 2003, reported to be associated with a form of heart disease called cardiac fibrosis

 

 

 

Dopamine autoagonist

Name
Tradename
Method
Notes
Side-effects

Talipexole

 

-dopamine agonist

-also has alpha-adrenergic agonist activity

- tested on 13 subjects with TS. 5 dropped out, 4 experienced intolerable side effects

.- Blinded evaluation of videotapes failed to show any statistically significant improvement in tic frequency or severity

- Not recommended for standard treatment for TS

 
         

 

 

 

Norepinephrine Reuptake Inhibitor

Name
Tradename
Method
Notes
Side-effects

Atomoxetine (formally known as Tomoxetine)

Strattera

 

- After 2-3 weeks of treatment, a patients mother reported reduction in tics and vocal tics eliminated. AHDH improved (source)

- Two children with ADHD developed tics while on Atomoxetine that did not fully resolve upon discontinuation (Parraga, Parraga, Harris)

- upset stomach, sporadic nausea, sudden vomiting

- sexual side effects

Reboxetine

 

Selective Norepinephrine Reuptake Inhibitor

   

Desipramine

-Norpramin

-Pertofrane

   

Can prolong QT interval (lead to sudden death)

 

 

 

Cannabis

Name
Tradename
Method
Notes
Side-effects

Marijuana

   

- significant reduction in tics in two studies (Mueller-Vahl, 2003)

 

Marinol

   

- some patients clearly benefit when taking Marinol at a doseage of 2.5 to 10mg twice a day

 

 

 

 

Calcium antagonists

Name
Tradename
Method
Notes
Side-effects

Nifedipine

ProcardiaXL

Acts on slow calcium channels invascular smooth muscle and myocardium, producing vasodilation

decrease in tic symptoms. 10mg 3 times daily

- dizziness, giddiness, headache, autonomic flushing, warmth, sweating, nasal congestion, sore throat

- nausea, constipation, flatulence

- dyspnea, cough, hpotension, wheezing, tachycardia, arrhythmias, fever, heart failure, muscle cramping

Verapamil

Isoptin

inhibits calcium transport into myocardialand vascular smooth muscle cells, resulting in inhibition of excitation contraction coupling and subsequent contraction

decrease in motor tics, improvement in mood, 20mg 3 times daily

- dizziness, headache, fatigue, constipation, abdominal discomfort

- bradycardia, hypotension, edema, heart block, sinus arrest, pulmonary edema

 

 

 

Benzodiazepine derivative

Name
Tradename
Method
Notes
Side-effects

Clonazepam

Klonopin (USA), Rivotril, Ravotril, or RIvatril, elsewhere

- GABA receptor antagonist

-sometimes useful in managing tics "since some of the premonitory sensations resemble obsessions and the tics may be viewed as 'compulsive' movements, anti-OCD medications also may be helpful"

 

Sedation, weight gain, impaired academic performance, social anxiety with school refusal in children and a worsening of attention in children with comorbid ADHD

 

 

 

Anticonvulsant

Name
Tradename
Method
Notes
Side-effects

Levetiracetam

Keppa

"antiepileptic drug with atypical mechanisms of action"

All 60 patients showed improvement (Awaad, Michon, Minarik)

- hair loss

- pins and needles sensation

- psychiatric symptoms ranging from irritability to depression

- headache

- nausea

Topiramate

Topamax

 

- the reduction in tics in some patients may be explained by its potentiation of GABA activity

- can be used for OCD

- no reports of it exacerbating movement disorders

- change in taste, pins and needles, cognitive deficiency, difficulty understanding concepts

- loss of appetits

- somnolence

- nausea

- upper respiratory tract infection

- osteroporosis

Lamotrigine

 

 

occasionally reported to cause tics, but they resolved completely within a month following cessation of the drug. Tics reappeared with the introduction of lamotrigine

 

 

 

 

Antiepileptic

Name
Tradename
Method
Notes
Side-effects

Carbmazepine

   

Reported to worsen tics in 8 patients while improving them in 1

Associated with the development of other movement disorders

 

 

 

Opiod

(http://grande.nal.usda.gov/ibids/index.php?mode2=detail&origin=ibids_references&therow=175030

Opiods may worsen tics - http://www.aafp.org/afp/990415ap/2263.html)

 

Name
Tradename
Method
Notes
Side-effects

Propoxyphene

       

Naltrexone

Vivitrol (USA), Revia, Depade (elsewhere)

 

-significant lessening of tics after treatment than with placebo

-reported to improve symptoms of TS, but also reports of it worsening TS

 

 

Oxycodone

       

 

 

 

Muscle Relaxant

Name
Tradename
Method
Notes
Side-effects

Carisoprodol

Soma

Centrally-acting muscle relaxant whose active metabolite is meprobamate

   

 

 

 

Anti-hypertensive

Name
Tradename
Method
Notes
Side-effects

Propranolol

Inderal

Non-selective beta blocker

   

 

 

 

Drugs to be added to the list in the future:

 

Ondansteron, a selective 5-HT3 antagonist at 8-16mg/day for 3 weeks has been associated with a decrease in severity of tics.

 

Baclofen, a GABA(B) autoreceptor agonist, has been found to markedly decrease the severity of motor and phonic tics in 95% of 264 patients with TS, however a double-blind, placebo-controlled, crossover trial of 9 patients with TS showed that the beneficial response to baclefen was due to improvement in overall impairment score rather than a reduction of tic activity.

 

Donepezil, a noncompetitive inhibitor of acetylcholinesterase, has been reported anecdotally to suppress tics.

 

Finasteride
http://ajp.psychiatryonline.org/cgi/content/short/164/12/1914?rss=1

 

Botox Injections

Also, the treatment is fairly downstream in the sense that it only inhibits your ability to perform the tic -- not the neurology causing the tic, the urge to engage in the tic, or the tic attempts themselves. There is some evidence to suggest that the premonitory urge to tic decreases following Botox, but I can see how it might feel like you have an 'unscratchable itch" for those in whom it doesn't.

 

Deep Brain Stimulation