I switched from aripiprazole (Abilify) to lurasidone (Latuda) for akathisia but still have tremor; how should I manage this?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 24, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Management of Persistent Tremor After Switching from Aripiprazole to Lurasidone

Your continued shakiness after switching from aripiprazole to lurasidone likely represents persistent akathisia or drug-induced parkinsonism that requires either dose reduction of lurasidone, addition of propranolol 20-40 mg twice daily, or switching to a lower-risk atypical antipsychotic such as quetiapine, olanzapine, or clozapine. 1

Understanding Your Current Situation

Why Lurasidone May Still Cause Movement Symptoms

  • Lurasidone carries a documented risk of akathisia and extrapyramidal symptoms, with akathisia being one of the five most consistently encountered adverse events, occurring with a number-needed-to-harm (NNH) ranging from 6 to 30 depending on dose. 2
  • Even though lurasidone is an atypical antipsychotic with lower EPS risk than typical agents, akathisia can occur in a minority of patients and may manifest as the "shakiness" you're experiencing. 3
  • A recent 2025 case report documented severe akathisia developing with lurasidone at low, introductory doses, which resolved completely only after discontinuation. 4

Distinguishing Between Akathisia and Tremor

Your "shakiness" could represent either:

  • Akathisia: Subjective inner restlessness with objective motor findings like pacing, foot tapping, or movements resembling stretching. 5
  • Drug-induced parkinsonism: Characterized by bradykinesia, tremors, and rigidity without the subjective restlessness component. 1

Immediate Management Algorithm

Step 1: Reduce Lurasidone Dose First

  • Lower your current lurasidone dose as the initial strategy, since both akathisia and parkinsonism with lurasidone can be managed effectively with dose adjustment. 3
  • This approach is preferred over adding more medications because it addresses the root cause. 1

Step 2: Add Propranolol if Dose Reduction Insufficient

  • If dose reduction is not practical or symptoms persist, add propranolol 20-40 mg twice daily, as lipophilic beta-blockers (especially propranolol) are the most effective treatments for akathisia. 6, 7
  • Propranolol has demonstrated efficacy specifically for antipsychotic-induced akathisia and was successfully used in a case of withdrawal akathisia with aripiprazole. 7

Step 3: Consider Switching to Lower-Risk Atypical

If symptoms continue despite dose reduction and propranolol, switch to quetiapine, olanzapine, or clozapine, which have minimal EPS risk compared to lurasidone. 1

  • Quetiapine and olanzapine carry significantly lower akathisia risk than lurasidone or aripiprazole. 1
  • Clozapine exhibits the lowest EPS risk among all antipsychotics and may even alleviate parkinsonian-like symptoms, though it requires regular blood monitoring for agranulocytosis. 1

Why Anticholinergics Are NOT First-Line

Limited Efficacy for Akathisia

  • Anticholinergic agents like benztropine are consistently helpful for parkinsonian symptoms but have variable efficacy in akathisia, unlike their reliable effectiveness for acute dystonia. 1
  • Anticholinergics should not be used routinely for preventing EPS and should be reserved only when dose reduction and switching strategies have failed. 1

Potential Adverse Effects

  • Anticholinergic medications can cause delirium, drowsiness, and paradoxical agitation, particularly problematic if you need to function normally. 1

Critical Monitoring Points

Document Specific Symptoms

Clarify whether you experience:

  • Subjective inner restlessness with urge to move (suggests akathisia) 5
  • Resting tremor, slowed movements, muscle stiffness (suggests parkinsonism) 1
  • Pacing, foot tapping, or inability to sit still (objective signs of akathisia) 5

Timeline Matters

  • Akathisia typically appears days to weeks after starting or increasing an antipsychotic dose. 6
  • The fact that symptoms persisted after switching from aripiprazole suggests you may be particularly susceptible to movement side effects from dopamine-modulating agents. 4

Common Pitfalls to Avoid

Don't Assume All Atypicals Are Equal

  • Both aripiprazole and lurasidone can cause significant akathisia despite being second-generation antipsychotics, as documented in a 2025 case report where both agents sequentially caused severe akathisia. 4
  • The partial dopamine agonist properties of aripiprazole and the serotonin-dopamine activity modulation of lurasidone do not eliminate akathisia risk. 4

Don't Continue Same Dose Hoping Symptoms Resolve

  • Most side effects with lurasidone like somnolence are transitory, but akathisia and EPS require active management through dose adjustment or medication change, not watchful waiting. 3

Don't Add Multiple Adjunctive Agents

  • Avoid polypharmacy by systematically trying dose reduction first, then a single adjunctive agent (propranolol), then switching—rather than layering multiple medications. 1

Long-Term Considerations

  • Monitor for tardive dyskinesia every 3-6 months using standardized scales, as the risk is approximately 5% per year in younger patients on long-term antipsychotics. 1
  • If you achieve symptom control with propranolol added to lurasidone, attempt to taper propranolol after 2-3 months of stability to determine if it remains necessary. 1

References

Guideline

Extrapyramidal Symptoms: Causes, Risk Factors, and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Akathisia Diagnosis and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Management of acute extrapyramidal effects induced by antipsychotic drugs.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 1997

Related Questions

What are the recommended steps to manage akathisia in a patient on Abilify (aripiprazole)?
Should a switch to Lurasidone be considered for a patient with a history of psychosis, autism, insomnia, and ADHD, who has gained significant weight on Abilify (aripiprazole)?
What is the best course of action for a 36 year old female patient taking lurasidone (latuda) 40mg for bipolar schizophrenia who complains of mood swings?
Does akathisia (involuntary movement disorder) improve with continued use of Abilify (aripiprazole)?
What is the mechanism behind extra pyramidal side effects (EPS)?
Can an 80-year-old man with a one-week-old herpes zoster rash that has not yet fully crusted be started on oral acyclovir, considering possible age‑related renal impairment?
Is it appropriate to initiate ondansetron (Zofran) for a short course when an adult patient starts or has dose changes of a GLP‑1 receptor agonist to prevent nausea?
What is the recommended diagnostic workup and initial treatment for an adult with nephrotic-range proteinuria?
Should a 24-year-old asymptomatic male with normal total cholesterol and triglycerides but borderline-high low-density lipoprotein (LDL) of 137 mg/dL be started on cholesterol‑lowering medication or antiplatelet therapy?
What antibiotics should be used for an otherwise healthy adult with a facial skin and soft‑tissue abscess, including options for penicillin allergy and for possible MRSA coverage?
What is the optimal anesthesia management for a patient with a prior central retinal vein occlusion, including preservation of ocular perfusion, avoidance of intra‑ocular pressure rise, maintenance of hemodynamic stability, and handling of antiplatelet or anticoagulant therapy?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.