Ingrezza (Valbenazine) for Confirmed Tardive Dyskinesia
Yes, Ingrezza (valbenazine) is specifically indicated and should be used for patients with confirmed moderate to severe tardive dyskinesia, as it is FDA-approved for this indication and represents first-line pharmacotherapy according to current guidelines. 1, 2, 3
When Valbenazine Is Appropriate
For confirmed tardive dyskinesia that is moderate to severe or disabling, valbenazine is the recommended first-line pharmacological treatment. 1, 2 The American Psychiatric Association specifically endorses VMAT2 inhibitors (valbenazine or deutetrabenazine) as the primary pharmacotherapy option. 1, 2
Key Clinical Considerations:
Valbenazine is FDA-approved specifically for tardive dyskinesia and demonstrated statistically significant improvement in the AIMS dyskinesia total score at 80 mg daily dosing. 3
The effect size is clinically meaningful - 40% of patients on valbenazine 80 mg/day achieved ≥50% reduction in AIMS dyskinesia score versus only 8.7% on placebo, yielding a number needed to treat (NNT) of 4. 4
Onset of benefit occurs within 2 weeks of treatment initiation, with once-daily dosing providing practical advantages. 5
Critical Diagnostic Distinction
Before prescribing valbenazine, confirm the diagnosis is actually tardive dyskinesia and not another movement disorder. 6 This distinction is essential because:
Classic tardive dyskinesia involves choreiform and athetoid movements (rapid involuntary facial movements, grimacing, chewing, tongue movements), NOT tremor as a primary feature. 6
If tremor is the predominant symptom, consider drug-induced parkinsonism instead, which presents with bradykinesia, tremors, and rigidity - this condition responds to anticholinergic agents like benztropine, whereas TD does not. 6
Anticholinergic medications are contraindicated for tardive dyskinesia and may actually worsen the condition. 2
Treatment Algorithm
Confirm TD diagnosis using clinical observation and baseline AIMS scoring before initiating treatment. 1
Assess severity - valbenazine is specifically recommended for moderate to severe or disabling TD. 1, 2
If clinically feasible, gradually withdraw the offending antipsychotic as the primary intervention when the underlying psychiatric condition allows. 2
If antipsychotic continuation is necessary, consider switching to atypical antipsychotics with lower D2 receptor affinity, or preferably clozapine, which has the lowest risk profile for movement disorders. 1
Initiate valbenazine 80 mg daily as first-line pharmacotherapy for persistent moderate to severe TD. 3, 4
Monitor response using AIMS at regular intervals (at least every 3-6 months). 2
Safety Profile
Discontinuation due to adverse events is rare - only 2.9% for valbenazine versus 1.6% for placebo (NNH of 76, not statistically significant). 4
Somnolence is the primary side effect (10.9% vs 4.2% placebo), with an NNH of 15. 4
QT interval prolongation is possible, requiring ECG monitoring consideration. 4
Valbenazine is approximately 15 times more likely to result in clinical response than discontinuation due to adverse events. 4
Common Pitfalls to Avoid
Do not use valbenazine for tremor-predominant presentations - these likely represent drug-induced parkinsonism, not TD. 6
Never use anticholinergic medications (benztropine, trihexyphenidyl) for TD - they are contraindicated and may worsen symptoms. 2
Do not delay treatment - TD may persist or become irreversible even after medication discontinuation, making early intervention critical. 1