Adult | Pediatric | ||||||
---|---|---|---|---|---|---|---|
Medication | Approved indications | Usual dosage | Maximum (mg/day) | Usual dosage | Maximum (mg/day) | Comments | |
ANTIDEPRESSANTS | |||||||
Tricyclic and tetracyclic antidepressants | |||||||
Secondary tricyclics | |||||||
Desipramine (Norpramin) | MDD | 100–200 mg/day (at bedtime or in divided doses) | 300 | Ages ≥ 13 years: 25–100 mg/day (at bedtime or in divided doses) | 150 | ||
Nortriptyline (Pamelor) | MDD | 75–100 mg/day (once daily or divided tid–qid) | 150 | Ages 6–12 years: 1–3 mg/kg/day (divided tid–qid | 150 | ||
Ages > 12 years: 30–50 mg/day (once daily or divided tid–qid | 150 | ||||||
Protriptyline (Vivactil) | MDD | 15–40 mg/day (divided tid–qid) | 60 | Ages ≥ 12 years: 15 mg/day (divided tid) | 60 | ||
Tertiary tricyclics | |||||||
Amitriptyline (Elavil) | MDD | 50–150 mg/day (at bedtime or in divided doses) | 300 | Ages ≥ 12 years: 50–100 mg/day (once daily or in divided doses) | 200 | ||
MDD, hospitalized patients | 100–200 mg/day (at bedtime or in divided doses) | 300 | |||||
Clomipramine (Anafranil) | OCD | 150–250 mg/day (at bedtime or in divided doses) | 250 | Ages ≥ 10 years: 100–200 mg/day (at bedtime or in divided doses) | 3 mg/kg/day or 200 mg/day, whichever is less | ||
Doxepin | Depression and/or anxiety | ||||||
Mild to moderate symptoms | 75–150 mg/day (at bedtime or in divided doses) | 150 | |||||
Severe symptoms | 300 mg/day (at bedtime or in divided doses) | 300 | |||||
Doxepin (Silenor) | Insomnia (sleep maintenance) | 3–6 mg at bedtime | 6 | ||||
Imipramine (Tofranil) | MDD | 50–150 mg/day (at bedtime or in divided doses) | 200 | Ages ≥ 13 years: 30–40 mg/day (at bedtime or in divided doses) | 100 | ||
MDD, hospitalized patients | 250–300 mg/day (in divided doses) | 300 | |||||
Nocturnal enuresis | Ages 6–12 years: 10–50 mg at bedtime | 50 | |||||
Ages > 12 years: 10–75 mg at bedtime | 75 | ||||||
Trimipramine (Surmontil) | MDD | 50–150 mg/day (at bedtime or in divided doses) | 200 | Ages ≥ 13 years: 50–100 mg/day (at bedtime or in divided doses) | 100 | ||
MDD, hospitalized patients | 250–300 mg/day (at bedtime or in divided doses) | 300 | |||||
Tetracyclics | |||||||
Amoxapine | MDD | 200–300 mg/day (at bedtime or in divided doses) | 400 | ||||
MDD, hospitalized patients | 200–300 mg/day (at bedtime or in divided doses) | 600 | |||||
Maprotiline | MDD | 75–150 mg/day (at bedtime or in divided doses) | 150 | ||||
MDD, hospitalized patients | 150–225 mg/day (at bedtime or in divided doses) | 225 | |||||
Selective serotonin reuptake inhibitor (SSRI) antidepressants | |||||||
Citalopram (Celexa) | MDD | 20–40 mg/day | 40 | ||||
Escitalopram (Lexapro) | MDD | 10–20 mg/day | 20 | Ages 12–17 years: 10–20 mg/day | 20 | ||
GAD | 10–20 mg/day | 20 | |||||
Fluoxetine (Prozac) | MDD | 20–80 mg/day in morning or divided bid; or 90 mg weekly† | 80 | Ages ≥ 8 years: 10–20 mg/day in morning | 20 | †Fluoxetine 90-mg delayed-release capsule | |
OCD | 20–60 mg/day in morning or divided bid | 80 | Ages ≥ 7 years: 20–60 mg/day in morning or divided bid | 60 | |||
Panic disorder | 20–60 mg/day | 60 | |||||
Bulimia nervosa | 20–60 mg/day | 60 | |||||
Fluoxetine (Sarafem) | PMDD | 20–60 mg/day† | 80 | †Administered throughout menstrual cycle or during luteal phase of menstrual cycle. | |||
Fluvoxamine | OCD | 100–300 mg/day (divided bid) | 300 | Ages 8–17 years: 50–200 mg/day (divided bid) | 200 | ||
Ages > 17 years: 100–300 mg/day (divided bid) | 300 | ||||||
Fluvoxamine extended-release (Luvox CR) | OCD | 100–300 mg/day at bedtime | 300 | ||||
Paroxetine (Paxil) | MDD | 20–50 mg/day in morning | 50 | ||||
Paroxetine extended-release (Paxil CR) | CR: 25–62.5 mg/day | 62.5 | |||||
GAD | 20–50 mg/day | 50 | |||||
Social anxiety disorder | 20–60 mg/day | 60 | Ages 8–17 years:* 10–60 mg/day in morning | 60 | *Off-label use. | ||
CR: 12.5–37.5 mg/day | 37.5 | ||||||
Panic disorder | 40 mg/day in morning CR: 12.5–75 mg/day in morning | 60 75 | |||||
OCD | 20–60 mg/day in morning | 60 | Ages 7–17 years:* 10–60 mg/day in morning | 60 | *Off-label use. | ||
PTSD | 20–50 mg/day in morning | 50 | |||||
PMDD | CR: 12.5–25 mg/ day in morning† | 25 | †Administered throughout menstrual cycle or during luteal phase of menstrual cycle. | ||||
Paroxetine mesylate (Brisdelle)† | Moderate to severe vasomotor symptoms associated with menopause | 7.5 mg/day at bedtime | — | †Limitations of Use: Not indicated for treatment of any psychiatric condition; contains a lower dosage than that used to treat psychiatric disorders. | |||
Sertraline (Zoloft) | MDD | 50–200 mg/day in morning | 200 | Ages ≥ 6 years:* 25–200 mg/day in morning | 200 | *Off-label use. | |
Social anxiety disorder | 50–200 mg/day | 200 | |||||
Panic disorder | 50–200 mg/day in morning | 200 | |||||
OCD | 50–200 mg/day in morning | 200 | Ages 6–12 years: 25–200 mg/day | 200 | |||
Ages 13–17 years: 50–200 mg/day | 200 | ||||||
PTSD | 50–200 mg/day in morning | 200 | |||||
PMDD | 50–200 mg/day in morning† | 150 | †Administered throughout menstrual cycle or during luteal phase of menstrual cycle. | ||||
Serotonin-norepinephrine reuptake inhibitor (SNRI) antidepressants | |||||||
Desvenlafaxine (Pristiq) | MDD | 50 mg/day | 50 | ||||
Duloxetine delayed-release (Cymbalta;† Drizalma Sprinkle††) | MDD | 40–60 mg/day (once daily or divided bid) | 120 | †Cymbalta must be swallowed whole; do not crush, chew, or open capsule. | |||
GAD | 60 mg/day | 120 | Ages 7–17 years: 30–60 mg/day | 120 | ††Drizalma may be swallowed whole (do not crush or chew capsule); opened and sprinkled over applesauce; or administered via nasogastric tube. | ||
Diabetic neuropathic pain | 60 mg/day | 60 | |||||
Musculoskeletal pain | 60 mg/day | 60 | |||||
Fibromyalgia | 60 mg/day | 60 | Ages 13–17 years:† 60 mg/day | 60 | †Cymbalta only; Drizalma is approved only in adults | ||
Levomilnacipran (Fetzima) | MDD | 40–120 mg/day | 120 | ||||
Milnacipran (Savella) | Fibromyalgia | 100 mg/day (divided bid) | 200 | ||||
Venlafaxine | MDD | 75–225 mg/day | 225 | ||||
Venlafaxine extended-release (Effexor ER) | MDD | 75–225 mg/day | 225 | ||||
GAD | 75–225 mg/day | 225 | |||||
Social anxiety disorder | 75 mg/day | 75 | |||||
Panic disorder | 75–225 mg/day | 225 | |||||
Venlafaxine besylate extended-release tablets (112.5 mg)† | MDD GAD | 112.5 mg once daily with food | 225 | †Do not initiate treatment with venlafaxine extended-release tablets. Use another venlafaxine extended-release product for initial dosage, titration, and dosages below 112.5 mg once daily. | |||
Norepinephrine-dopamine reuptake inhibitor (NDRI) antidepressant (putative§) | |||||||
Bupropion immediate-release | MDD | 300 mg/day (divided tid) | 150 mg/dose; 450 mg/day | §Bupropion’s precise mechanism of action is not known. | |||
ADHD* | 300 mg/day (divided tid) | † | Ages ≥ 6 years: 1.4–6.0 mg/kg/day (divided bid) | † | *Off-label use. | ||
†Maximum dosing (adult and pediatric) for bupropion IR: 150 mg/dose; 450 mg/day | |||||||
Bupropion sustained-release (Wellbutrin SR) | MDD | SR: 300 mg/day (divided bid) | 400 | ||||
ADHD* | SR: 300 mg/day (divided bid) | 400 | Ages ≥ 12 years: 3–6 mg/kg/day (divided bid) | 400 | *Off-label use. | ||
Bupropion extended-release | |||||||
Bupropion XL | MDD, seasonal affective disorder | 300 mg/day in morning | 450 | ||||
ADHD* | 300 mg/day in morning | 300 | Ages ≥ 12 years: 3–6 mg/kg/day in morning | 400 | *Off-label use. | ||
Aplenzin | MDD, seasonal affective disorder | 348 mg/day in morning | 522 | ||||
Multimodal serotonin antagonist antidepressants | |||||||
Nefazodone‡ | MDD | 300–600 mg/day (divided bid) | 600 | ‡Risk of hepatic failure associated with nefazodone hydrochloride treatment. | |||
Depression | Refer to manufacturer’s full prescribing information for dosing guidelines and titration schedule. | 600 | |||||
Trazodone | MDD | 150–300 mg/day (divided bid–tid) | 400 | ||||
Insomnia* | 25–100 mg/day at bedtime | 200 | *Off-label use. | ||||
Trazodone extended-release† | MDD | 150–375 mg/day at bedtime | 375 | †The Oleptro brand name has been discontinued in the United States. | |||
Serotonin-modulating antidepressants | |||||||
Vilazodone (Viibryd) | MDD | 20–40 mg/day | 40 | ||||
Vortioxetine (Trintellix) | MDD | 20 mg/day | 20† | †Dosage should not exceed 10 mg/day in CYP2D6 poor metabolizers or be administered with strong CYP2D6 inhibitors. | |||
Noradrenergic-specific serotonin antidepressant (NaSSA) | |||||||
Mirtazapine (Remeron) | MDD | 15–45 mg/day at bedtime | 45 | ||||
Selective serotonin 1A receptor partial agonist antidepressant | |||||||
Gepirone extended-release (Exxua) | MDD | Start with 18.2 mg/day. Dosage may be increased to 36.3 mg/day on day 4, and may be further titrated to 54.5 mg/day after day 7 and to 72.6 mg/day after an additional week. | 72.6 | ||||
Neuroactive steroid GABA-A receptor positive allosteric modulator (PAM) antidepressants | |||||||
Brexanolone injection (Zulresso)‡ | PPD in patients ages 15 years and older | Administered as a continuous IV infusion over 60 hours (2.5 days).† | — | ‡Available only through a REMS drug safety program. | |||
Refer to manufacturer’s full prescribing information for recommended dosing. | |||||||
Zuranolone capsules (Zurzuvae) | PPD | Refer to manufacturer’s full prescribing information for recommended dosing. | — | †A health care provider must be available on site to continuously monitor the patient, and intervene as necessary, for the duration of the infusion. | |||
Monoamine oxidase inhibitor (MAOI) antidepressants | |||||||
Isocarboxazid (Marplan) | MDD and atypical depression | 40–60 mg/day (divided bid–qid) | 60 | ||||
Phenelzine (Nardil) | MDD and atypical depression | 40–60 mg/day in divided doses† | 90 | †After maximum benefit is achieved, dosage should be reduced over several weeks. Maintenance dosage can range from 15 mg every other day to 15 mg once daily. | |||
Selegiline transdermal patch (Emsam) | MDD | 6–12 mg patch per 24 hours | 12 | ||||
Selegiline hydrochloride (Zelapar ODT [orally disintegrating tablets]) | Management of patients with Parkinson’s disease being treated with levodopa/carbidopa | 1.25 mg given once daily for at least 6 weeks. After 6 weeks, daily dosage may be escalated up to 2.5 mg. | 2.5 | ||||
Tranylcypromine (Parnate) | MDD and atypical depression | 30 mg/day in divided doses | 60 | ||||
NMDA receptor antagonist antidepressants | |||||||
Dextromethorphan hydrobromide/bupropion hydrochloride extended-release tablets (Auvelity) | MDD | Start with 1 tablet (45 mg/105 mg) daily taken in the morning. After 3 days, increase to maximum recommended dosage of 1 tablet taken twice daily, separated by at least 8 hours. | Do not exceed two 1-tablet doses taken within the same day. | ||||
Esketamine nasal spray (Spravato)‡ | Treatment-resistant depression | Refer to manufacturer’s full prescribing information for recommended dosing.† | — | ‡Available only through a REMS drug safety program. | |||
Depressive symptoms with acute suicidal ideation or behavior in patients with MDD | — | †Administer intranasally under the supervision of a health care provider. | |||||
Ketamine | Relief of acute depression with suicidal ideation* | 0.5 mg/kg IV infusion over 40 minutes | — | *Off-label use. | |||
ANXIOLYTICS | |||||||
Benzodiazepine GABA-A receptor PAMs | |||||||
Alprazolam (Xanax) | GAD | 0.25–0.5 mg tid | 4 | ||||
Panic disorder | 1.5–9 mg/day (divided tid) | 10 | |||||
Alprazolam extended-release (Xanax XR) | GAD | 3–6 mg/day | 6 | ||||
Chlordiazepoxide | GAD, mild to moderate | 5–10 mg tid–qid | † | Ages ≥ 6 years: 5–10 mg bid–tid | † | †There is no well-established chlordiazepoxide maximum dosage for treatment of GAD. | |
GAD, severe | 20–25 mg tid–qid | † | |||||
Acute alcohol withdrawal | 50–100 mg prn | 300 | |||||
Clonazepam (Klonopin) | Panic disorder | 1–4 mg/day (divided bid) | 4 | ||||
Clorazepate | GAD | 15–30 mg/day (at bedtime or divided bid) | 60 | ||||
Acute alcohol withdrawal | Refer to manufacturer's full prescribing information for recommended dosing guidelines and titration schedules. | — | |||||
Diazepam (Valium) | GAD | 2–10 mg bid–qid | 40 | ||||
Acute alcohol withdrawal | 10 mg tid–qid for first 24 hours; then 5 mg tid–qid prn | — | |||||
Lorazepam (Ativan) | GAD | 2–6 mg/day (divided bid–tid) | 10 | ||||
Anxiety-associated insomnia | 2–4 mg at bedtime | 4 | |||||
Lorazepam injection (Ativan Injection) | Acute agitation* | 0.5–1 mg IM prn every 30–60 minutes | — | *Off-label use. | |||
Lorazepam extended-release capsules (Loreev XR) | Anxiety disorders in adults who are receiving stable, evenly divided, three-times-daily dosing with lorazepam tablets | Refer to manufacturer's full prescribing information for recommended dosing. | — | ||||
Oxazepam | GAD | 10–30 mg tid–qid | 120 | ||||
Acute alcohol withdrawal | 15–30 mg tid–qid | — | |||||
Serotonin-1A receptor partial agonist | |||||||
Buspirone | GAD | 20–30 mg/day (divided bid–tid) | 60 | ||||
AGENTS FOR TREATMENT OF INSOMNIA | |||||||
Benzodiazepine GABA-A receptor PAMs | |||||||
Estazolam | Insomnia (sleep onset/maintenance; nocturnal or early-morning awakening) | 1–2 mg at bedtime | 2 | ||||
Flurazepam (Dalmane) | Insomnia (sleep onset/maintenance) | 15–30 mg at bedtime | 30 | ||||
Quazepam (Doral) | Insomnia (sleep onset; nocturnal or early-morning awakening) | 7.5–15 mg at bedtime | 15 | ||||
Temazepam (Restoril) | Insomnia (sleep onset/maintenance) | 7.5–30 mg at bedtime | 30 | ||||
Triazolam (Halcion) | Insomnia (sleep onset/maintenance) | 0.125–0.5 mg at bedtime | 0.5; 0.25 in elderly | ||||
Nonbenzodiazepine GABA-A receptor PAMs | |||||||
Eszopiclone (Lunesta) | Insomnia (sleep onset/maintenance) | 1–3 mg at bedtime | 3 | ||||
Zaleplon (Sonata) | Insomnia (middle-of-night awakening) | 10–20 mg at bedtime | 20 | ||||
Zolpidem (Ambien) | Insomnia (sleep onset) | 5–10 mg at bedtime | 10 | ||||
Zolpidem extended-release (Ambien CR) | Insomnia (sleep onset/maintenance) | 6.5–12.5 mg | 12.5 | ||||
Zolpidem sublingual (SL) (Intermezzo) | Insomnia (sleep initiation)† | Women: 1.75 mg prn Men: 3.5 mg prn | Once per night | †Take as needed if unable to return to sleep after middle-of-night-awakening. | |||
Melatonin receptor agonists | |||||||
Ramelteon (Rozerem) | Insomnia (sleep onset) | 8 mg at bedtime | 8 | ||||
Tasimelteon (Hetlioz) | Non-24-hour sleep-wake disorder | 20 mg at bedtime | 20 | ||||
Nighttime sleep disturbance in Smith-Magenis syndrome (SMS) in patients ages 16 years and older | 20 mg taken 1 hour before bedtime | 20 | 20 mg taken 1 hour before bedtime | 20 | |||
Nighttime sleep disturbance in SMS in pediatric patients ages 3–15 years | 20 mg taken 1 hour before bedtime; if weight less than 28 kg, 0.7 mg/kg taken 1 hour before bedtime | 0.7 mg/kg | |||||
Orexin receptor antagonists | |||||||
Daridorexant (Quviviq) | Insomnia (sleep onset/maintenance) | 25–50 mg at bedtime | 50 | ||||
Lemborexant (Dayvigo) | Insomnia (sleep onset/maintenance) | 5–10 mg once per night, immediately before going to bed, with at least 7 hours remaining before the planned time of awakening | 10 | ||||
Suvorexant (Belsomra) | Insomnia (sleep onset/maintenance) | 10–20 mg at bedtime | 20 | ||||
ANTIPSYCHOTICS | |||||||
First-generation (typical) antipsychotics | |||||||
Chlorpromazine | Psychotic disorders | 200–600 mg/day (divided tid–qid) | 1,000 | ||||
Acute manic states, hospitalized patients | 200–800 mg/day (divided tid–qid) | 2,000 | |||||
Chlorpromazine injection | Acute agitation, hospitalized patients | 25 mg IM, repeat 25–50 mg in 1 hour; up to 400 mg IM every 4–6 hours prn | — | ||||
Fluphenazine | Psychotic disorders | 2.5–10 mg/day (divided tid–qid) | 40 | ||||
Fluphenazine hydrochloride injection | Acute agitation | 2.5–10 mg/day IM every 6–8 hours prn | 10 | ||||
Fluphenazine decanoate injection | Management of psychotic disorders and schizophrenia | 25–50 mg IM every 3 weeks† | — | †Approximate conversion ratio of decanoate to oral is 12.5 mg (0.5 mL) every 3 weeks for every 10 mg of oral fluphenazine daily. | |||
Haloperidol | Psychotic disorders | 0.5–5 mg bid–tid | 100 | Ages 3–12 years: 0.05–0.15 mg/ kg/day | 0.15 mg/kg/day | ||
Ages > 12 years: 0.5–5 mg bid–tid | 15 | ||||||
Tourette’s disorder | 0.5–5 mg bid–tid | 100 | Ages 3–12 years: 0.05–0.075 mg/ kg/day | 0.15 mg/kg/day | |||
Ages > 12 years: 0.5–5 mg bid–tid | 15 | ||||||
Behavioral disorders, severe | Ages 3–12 years: 0.05–0.075 mg/ kg/day | 0.15 mg/kg/day | |||||
Ages > 12 years: 0.5–5 mg bid–tid | 15 | ||||||
Haloperidol lactate injection (Haldol Injection) | Acute psychosis | 2–10 mg IM every 4–8 hours prn | 20 | ||||
Haloperidol decanoate injection (Haldol Decanoate) | Management of psychotic disorders and schizophrenia | 50–200 mg IM every month | — | ||||
Loxapine (Loxitane) | Psychotic disorders | 60–100 mg/day in divided doses | 250 | ||||
Loxapine inhalation (Adasuave)‡ | Acute agitation | 10 mg/day† | 10 | ‡Available only through a REMS drug safety program. †Must be administered by a health care professional. | |||
Perphenazine | Psychotic disorders | 4–8 mg tid | 24 | ||||
Psychotic disorders, hospitalized patients | 8–16 mg bid–qid | 64 | |||||
Pimozide (Orap) | Tourette’s disorder | 2–10 mg/day | 10 | Ages ≥ 12 years: 0.05–0.2 mg/ kg/day | 0.2 mg/kg/day, up to 10 mg/day | ||
Thioridazine | Psychotic disorders | 200–800 mg/day (divided bid–qid) | 800 | ||||
Thiothixene | Psychotic disorders | 20–30 mg/day in divided doses | 60 | ||||
Trifluoperazine | Psychotic disorders | 15–20 mg/day (once daily or divided bid) | 40 | Ages 6–12 years: 1 mg/day (once daily or divided bid) | 15 | ||
Ages ≥ 13 years: 15–20 mg/day (once daily or divided bid) | 40 | ||||||
Nonpsychotic anxiety | 1–2 mg bid | 6 | |||||
Second-generation (atypical) antipsychotics | |||||||
Aripiprazole (Abilify) | Schizophrenia | 10–15 mg/day | 30 | Ages 13–17 years: 10 mg/day | 30 | ||
Bipolar I disorder | 10–15 mg/day | 30 | Ages 10–17 years: 10 mg/day | 30 | |||
MDD, as adjunctive therapy with antidepressants | 2–15 mg/day | 15 | |||||
Tourette’s disorder | Ages 6–18 years, < 50 kg: 5 mg/day | 10 | |||||
Ages 6–18 years, ≥ 50 kg: 10 mg/day | 20 | ||||||
Irritability associated with autism spectrum disorder | Ages 6–17 years: 5–10 mg/day | 15 | |||||
Aripiprazole long-acting IM injection (Abilify Maintena) | Schizophrenia | 300–400 IM every month | — | ||||
Aripiprazole lauroxil long-acting IM injection (Aristada) | Schizophrenia | 441–882 IM every 4–6 weeks | — | ||||
Asenapine SL (Saphris) | Schizophrenia | 10–20 mg/day SL (divided bid) | 20 | ||||
Bipolar I disorder, monotherapy | 10–20 mg/day SL (divided bid) | 20 | Ages 10–17 years: 5–10 mg/day SL (divided bid) | 20 | |||
Bipolar I disorder, as adjunctive therapy with lithium or valproate | 10 mg/day SL (divided bid) | 20 | |||||
Asenapine transdermal system (Secuado) | Schizophrenia | One 3.8 mg patch every 24 hours; may increase dosage to 5.7 mg/24 hours or 7.6 mg/24 hours after 1 week | 7.6 | ||||
Brexpiprazole (Rexulti) | Schizophrenia | 2–4 mg/day | 4 | Ages 13–17 years: 2–4 mg/day | 4 | ||
MDD, as adjunctive therapy with antidepressants | 2 mg/day | 3 | |||||
Second-generation (atypical) antipsychotics (continued) | |||||||
Brexpiprazole (Rexulti) (continued) | Agitation associated with dementia due to Alzheimer’s disease‡ | 2 mg/day | 3 | ‡Limitations of use: Not indicated as an as-needed (prn) treatment for this indication; not approved for treatment of dementia-related psychosis WITHOUT agitation associated with dementia due to Alzheimer’s disease | |||
Cariprazine (Vraylar) | Schizophrenia | 1.5–6 mg/day | 6 | ||||
Bipolar I disorder | 3–6 mg/day | 6 | |||||
Bipolar depression | 1.5–3 mg/day | 3 | |||||
MDD, as adjunctive therapy with antidepressants | 1.5–3 mg/day | 3 | |||||
Clozapine (Clozaril)‡ | Schizophrenia, refractory | 150–300 mg bid | 900 | ‡Available only through a REMS drug safety program. | |||
Schizophrenia with high suicide risk | 150–300 mg bid | 900 | |||||
Iloperidone (Fanapt) | Schizophrenia | 6–12 mg bid | 24 | ||||
Lumateperone (Caplyta) | Schizophrenia | 42 mg/day | 42 | ||||
Bipolar depression, as monotherapy or as adjunctive therapy with lithium or valproate | 42 mg/day | 42 | |||||
Lurasidone (Latuda) | Schizophrenia | 40–160 mg/day | 160 | Ages 10–17 years: 40–80 mg/day | 80 | ||
Bipolar depression, as adjunctive therapy with lithium or valproate | 20–120 mg/day | 120 | |||||
Bipolar depression, as monotherapy | 20–120 mg/day | 120 | Ages 10–17 years: 20–80 mg/day | 80 | |||
Olanzapine (Zyprexa) | Schizophrenia | 10–20 mg/day | 20 | Ages ≥ 13 years: 10 mg/day | 20 | ||
Bipolar I disorder | 5–20 mg/day | 20 | Ages ≥ 13 years: 10 mg/day | 20 | |||
Olanzapine IM injection (Zyprexa Intramuscular) | Acute agitation | 10 mg IM; may repeat after 2 hours one time; repeat prn 4 hours after second dose | 30 | ||||
Olanzapine long-acting IM injection (Zyprexa Relprevv)‡ | Schizophrenia | Refer to manufacturer's recommended dosing guidelines and titration schedules. | ‡Available only through a REMS drug safety program. | ||||
Olanzapine/fluoxetine (Symbyax) | Bipolar I disorder, acute depressive episodes | 6 mg/25 mg/day– 12 mg/50 mg/ day | 12/50 | Ages 10–17 years: 3 mg/25 mg/day | 12/50 | ||
Treatment-resistant depression | 6 mg/25 mg/day | 12/50 | |||||
Olanzapine/samidorphan (Lybalvi) | Schizophrenia | Starting: 5 mg/10 mg or 10 mg/10 mg | 20/10 | ||||
Recommended: 10 mg/10 mg, or 15 mg/10 mg, or 20 mg/10 mg | |||||||
Bipolar I disorder, manic or mixed episodes, as monotherapy | Starting: 10 mg/10 mg or 15 mg/10 mg | 20/10 | |||||
Recommended: 5 mg/10 mg, or 10 mg/10 mg, or 15 mg/10 mg, or 20 mg/10 mg | |||||||
Bipolar I disorder, as adjunctive therapy with lithium or valproate | Starting: 10 mg/10 mg | 20/10 | |||||
Recommended: 10 mg/10 mg, or 15 mg/10 mg, or 20 mg/10 mg | |||||||
Paliperidone (Invega) | Schizophrenia | 6 mg/day | 12 | Ages 12–17 years: 3 mg/day | 12 | ||
Paliperidone palmitate long-acting IM injection | Schizoaffective disorder | † | — | †Refer to manufacturer’s full prescribing information for dosing guidelines. | |||
Invega Sustenna (IM monthly injection) | † | — | |||||
Invega Trinza (IM injection every 3 months) | Patients who have been adequately treated with once- a-month Invega Sustenna for at least 4 months | Depends on previous Invega Sustenna once-a-month dosage† | — | ||||
Invega Hafyera (IM injection every 6 months) | Patients who have been adequately treated with either 1) once-a-month Invega Sustenna for at least 4 months or 2) every-3-month Invega Trinza for at least one 3-month cycle | Depends on previous Invega Sustenna once-a-month dosage† | — | †Refer to manufacturer's full prescribing information for dosing guidelines. | |||
Pimavanserin (Nuplazid) | Hallucinations and delusions associated with Parkinson’s disease | 34 mg taken orally as two 17-mg tablets once daily, without titration | 34 | ||||
Quetiapine (Seroquel) | Schizophrenia | 150–750 mg/day (divided bid–tid) | 750 | Ages 13–17 years: 400–800 mg/day (divided bid–tid) | 800 | ||
Bipolar I disorder, acute manic/ mixed episodes | 400–800 mg/day (divided bid) | 800 | Ages 10–17 years: 400–600 mg/day (divided bid–tid) | 600 | |||
Bipolar I disorder, depressive episodes | 300 mg/day at bedtime | 300 | |||||
Quetiapine extended-release (Seroquel XR) | Schizophrenia | 400–800 mg/day | 800 | Ages 13–17 years): 400–800 mg/day | 800 | ||
Bipolar I disorder, acute manic/ mixed episodes | 400–800 mg bid | 800 | Ages 10–17 years): 400–600 mg/day | 600 | |||
Bipolar I disorder, depressive episodes | 300 mg/day at bedtime | 300 | |||||
MDD, as adjunctive therapy with antidepressants | 150–300 mg/day | 300 | |||||
Risperidone (Risperdal) | Schizophrenia | 4–8 mg/day (once daily or divided bid) | 16 | Ages 13–17 years: 1–6 mg/day (once daily or divided bid) | 6 | ||
Bipolar I disorder, acute manic/ mixed episodes | 1–6 mg/day (once daily or divided bid) | 6 | Ages 10–17 years: 1–2.5 mg/day (once daily or divided bid) | 6 | |||
Irritability associated with autism spectrum disorder | Ages 5–17 years, weight < 20 kg: 0.5 mg/day (once daily or divided bid)† | 3 | †Weight < 20 kg: Start at 0.25 mg/day before increasing dosage. | ||||
Ages 5–17 years, weight ≥ 20 kg: 1 mg/day (once daily or divided bid)† | 3 | †Weight ≥ 20 kg: Start at 0.5 mg/day before increasing dosage. | |||||
Risperidone long-acting IM injection (Risperdal Consta) | Schizophrenia | 25–50 mg IM every 2 weeks | — | ||||
Bipolar I disorder | 25–50 mg IM every 2 weeks | — | |||||
Ziprasidone (Geodon) | Schizophrenia | 20 mg bid | 160 | ||||
Bipolar I disorder | 80–160 mg/day (divided bid) | 160 | |||||
Ziprasidone IM injection (Geodon Injection) | Acute agitation | 10 mg IM every 2 hours prn or 20 mg IM every 4 hours prn | — | ||||
MOOD STABILIZERS | |||||||
Lithium | |||||||
Lithium carbonate | Bipolar disorder | 900–1,200 mg/day (divided tid–qid)† | 2,400 | Ages ≥ 6 years, weight < 30 kg: 15–40 mg/kg/day (divided tid–qid)† | 60 mg/kg/day | †Dosage adjustment based on clinical response and trough levels of serum lithium between 0.6 and 1.2 mEq/L. | |
Ages ≥ 6 years, weight ≥ 30 kg: 15–40 mg/kg/day (divided tid–qid)† | 60 mg/kg/day, up to 2,400 mg | ||||||
Lithium extended-release (Lithobid) | Bipolar disorder | 900–1,800 mg/day (divided bid–tid) | 1,800 | Ages ≥ 6 years, weight < 30 kg: 15–40 mg/kg/day (divided tid–qid) | 60 mg/kg/day | ||
Ages ≥ 6 years, weight ≥ 30 kg: 15–40 mg/kg/day (divided tid–qid) | 60 mg/kg/day, up to 1,800 mg | ||||||
Anticonvulsants | |||||||
Carbamazepine (Tegretol) | Bipolar I disorder* | 800–1,200 mg/day (divided bid–qid) | 1,600 | *Off-label use. | |||
Carbamazepine extended-release (Equetro,† Tegretol XR) | Bipolar I disorder | 400–600 mg bid | 1,600 | †Equetro is the only carbamazepine formulation approved for the treatment of bipolar I disorder. | |||
Gabapentin (Neurontin) | Postherpetic neuralgia | 300–600 mg tid | 1,800 | ||||
Neuropathic pain* | 300–1,200 mg tid | 3,600 | *Off-label use. | ||||
Bipolar I disorder* | 600–3,600 mg/day (divided tid) | 3,600 | *Off-label use. | ||||
GAD* | 600–3,600 mg/day (divided tid) | 3,600 | *Off-label use. | ||||
Lamotrigine (Lamictal, Lamictal XR) | Bipolar I disorder | †Refer to manufacturer’s titration schedules, particularly for patients taking valproate or enzyme‐inducing medications concomitantly. Lamictal Starter/Titration Kits are available to guide lamotrigine dosing for monotherapy as well as comedication scenarios. | |||||
Monotherapy† | 200 mg/day | 200 | |||||
With valproate† | 100 mg/day | 100 | |||||
With enzyme inducers (e.g., carbamazepine)† | 200 mg bid | 400 | |||||
Bipolar depression* | 50–200 mg/day | 200 | *Off-label use. | ||||
Oxcarbazepine (Trileptal) | Bipolar I disorder* | 1,200–2,400 mg/ day (once daily or divided bid) | 2,400 | *Off-label use. | |||
Oxcarbazepine extended- release (Oxtellar XR) | |||||||
Pregabalin (Lyrica) | GAD* | 300 mg bid | 600 | *Off-label use. | |||
Fibromyalgia | 150–225 mg bid | 450 | |||||
Diabetic neuropathy | 100 mg tid | 300 | |||||
Neuropathic pain associated with spinal cord injury | 300 mg/day within 1 week | 600 | |||||
Postherpetic neuralgia | 300 mg/day within 1 week | 600 | |||||
Pregabalin extended-release (Lyrica CR) | Pain—diabetic peripheral neuropathy | 165 mg/day | 330 | ||||
Pain—postherpetic neuralgia | 165 mg/day | 660 | |||||
Topiramate (Topamax) | Bulimia nervosa* | 300–400 mg/day (divided bid) | 400 | *Off-label use. | |||
Depressive disorders, as adjunctive therapy with antidepressants* | 100–200 mg/day (divided bid) | — | *Off-label use. | ||||
Alcohol use disorder* | 300 mg/day in divided doses | 300 | *Off-label use. | ||||
Valproate, divalproex sodium (Depakote, Depakote ER) | Bipolar I disorder, manic episodes | 15–20 mg/kg/day Rapid oral loading:† 20–30 mg/kg/day | 60 mg/kg/ day | †In treatment of acute mania, a rapid oral loading regimen may be used, with dosage increases (based on response/tolerance) of 250–500 mg every 1–3 days until serum concentrations are between 45 and 125 mcg/mL. | |||
Delayed‐release tablets (Depakote): Take in divided doses. | |||||||
Extended‐release tablets (Depakote ER): Take once daily. | |||||||
PSYCHOSTIMULANTS FOR TREATMENT OF ADHD AND NARCOLEPSY | |||||||
Amphetamine formulations | |||||||
Amphetamine extended- release (Dyanavel XR) | ADHD in patients ages 6 years and older† | Starting dose is 2.5 mg or 5 mg once daily taken in the morning. Increase ***in increments of 2.5–10 mg/day every 4–7 days. | 20 | Starting dose is 2.5 mg or 5 mg once daily taken in the morning. Increase in increments of 2.5–10 mg/day every 4–7 days. | 20 | †Safety and effectiveness have been established in pediatric patients ages 6–17 years, but not in those younger than 6 years. | |
Amphetamine/dextroamphetamine (Adderall) | ADHD | 5–40 mg/day (once daily or divided bid) | 40 | Ages 3–5 years: 2.5–40 mg/day (once daily or divided bid) | 40 | ||
Ages ≥ 6 years: 5–40 mg/day (once daily or divided bid) | 40 | ||||||
Amphetamine/dextroamphetamine (Adderall) (continued) | Narcolepsy† | 5–60 mg/day in divided doses | 60 | 5–60 mg/day in divided doses | 60 | †Only the immediate‐release Adderall tablets are approved for treatment of narcolepsy. | |
Amphetamine/dextroamphetamine extended-release (Adderall XR) | ADHD | 20 mg/day in morning | 60 | Ages 6–12 years: 10 mg/day in morning | 30 | ||
Ages 13–17 years: 10–20 mg/day in morning | 40 | ||||||
Dextroamphetamine (Dexedrine) | ADHD | Ages ≥ 6 years: 5–40 mg/day (once daily or divided bid) | 40 | ||||
Narcolepsy | 5–60 mg/day (once daily or divided bid) | 60 | Ages ≥ 12 years: 5–60 mg/day (once daily or divided bid) | 60 | |||
Methamphetamine (Desoxyn) | ADHD | 20–25 mg/day (once daily or divided bid) | 25 | Ages ≥ 6 years: 20–25 mg/day (once daily or divided bid) | 25 | ||
Lisdexamfetamine (Vyvanse) | ADHD | 30–70 mg/day in morning | 70 | Ages ≥ 6 years: 30–70 mg/day in morning | 70 | ||
Binge-eating disorder | 50–70 mg/day in morning | 70 | |||||
Methylphenidate formulations | |||||||
Dexmethylphenidate (Focalin) | ADHD | 5–10 mg/day (divided bid) | 20 | Ages ≥ 6 years: 5–20 mg/day (divided bid) | 20 | ||
Dexmethylphenidate extended-release (Focalin XR) | 20–40 mg/day in morning | 40 | Ages ≥ 6 years: 10–30 mg/day in morning | 30 | |||
Methylphenidate | |||||||
Short-acting† | †Short-acting (IR) methylphenidate formulations have durations of action of 3–5 hours and generally require two- or three-times-daily dosing. | ||||||
Ritalin, Methylin | ADHD | 20–30 mg/day (divided bid–tid) | 60 | Ages ≥ 6 years: 15–30 mg/day (divided bid–tid) | 60 | ||
Narcolepsy | 20–30 mg/day (divided bid–tid) | 60 | |||||
Intermediate-acting† | †Intermediate-acting (extended-release, single pulse) methylphenidate formulations have durations of action of approximately 8 hours, with once- or twice-daily dosing. | ||||||
Metadate ER | ADHD | 20–40 mg/day (once daily or divided bid) | 60 | Ages ≥ 6 years: 20 mg/day (once daily or divided bid) | 60 | ||
Narcolepsy | 20–30 mg/day (once daily or divided bid) | 60 | |||||
Long-acting† | ADHD | †Long-acting (extended-release, dual pulse) methylphenidate formulations have durations of action of approximately 8–12 hours, with once-daily dosing in the morning. | |||||
Aptensio XR | 10–60 mg/day in morning | 60 | Ages ≥ 6 years: 10–60 mg/day in morning | 60 | |||
Concerta | 18–72 mg/day in morning | 72 | Ages 6–12 years: 18–54 mg/day in morning | 54 | |||
Ages 13–17 years: 18–72 mg/day in morning | 72 | ||||||
Daytrana Transdermal System | 10–30 mg patch per day† | 30 | Ages ≥ 6 years: 10–30 mg patch per day | 30 | †Wear patch for 9 hours; remove for 15 hours. | ||
Metadate CD, Quillivant XR, Ritalin LA | 20–60 mg/day in morning | 60 | Ages ≥ 6 years: 20–60 mg/day in morning | 60 | |||
Other psychostimulants | |||||||
Armodafinil (Nuvigil) | Narcolepsy Sleep apnea | 150–250 mg/day in morning | 250 | ||||
Modafinil (Provigil) | Narcolepsy Sleep apnea | 200 mg/day in morning | 400 | ||||
Calcium, magnesium, potassium, and sodium oxybates (Xywav)‡ | Idiopathic hypersomnia | Refer to manufacturer's full prescribing information for once-nightly and twice-nightly dosing guidelines. | 6–9 g | ‡Available only through a REMS drug safety program. | |||
Narcolepsy | 9 g | Ages ≥ 7 years: dosage based on body weight | Based on body weight† | †Dosages > 9 g/night have not been studied and should not be administered. | |||
NONPSYCHOSTIMULANTS FOR TREATMENT OF ADHD | |||||||
Selective norepinephrine reuptake inhibitors | |||||||
Atomoxetine (Strattera) | ADHD | 80–100 mg/day (divided bid) | 100 | Ages ≥ 6 years, weight < 70 kg: 1.2 mg/kg/day (divided bid) | 1.4† | †Maximum for children weighing less than 70 kg: 1.4 mg/kg/day; maximum dosage for adult and pediatric is 100 mg/day. | |
Ages ≥ 6 years, weight ≥ 70 kg: 80 mg/day (divided bid) | 100 | ||||||
Viloxazine extended-release (Qelbree) | ADHD | 200 mg/day | 600 | Ages ≥ 6 years: 100 mg/day | 400 | ||
Alpha-2 adrenergic receptor agonists | |||||||
Clonidine extended-release (Kapvay) | ADHD | Ages ≥ 6 years: 0.2–0.4 mg/day (divided bid) | 0.4 | ||||
Guanfacine extended-release (Intuniv) | ADHD | Ages 6–17 years: 0.05–0.12 mg/kg/day (1–7 mg/day) | † | †Dosages >4 mg/day (ages 6–12 years) and >7 mg/day (ages 13–17 years) have not been evaluated. | |||
AGENTS FOR TREATMENT OF COGNITIVE DISORDERS | |||||||
Acetylcholinesterase inhibitors | |||||||
Donepezil (Aricept) | Alzheimer’s disease, mild to moderate | 5–10 mg/day | 10 | ||||
Alzheimer’s disease, moderate to severe | 10–23 mg/day | 23 | |||||
Galantamine (Razadyne) | Alzheimer’s disease, mild to moderate | 8–12 mg bid | 24 | ||||
Galantamine extended- release (Razadyne ER) | Alzheimer’s disease, mild to moderate | 16–24 mg/day | 24 | ||||
Rivastigmine (Exelon) | Alzheimer’s disease, mild to severe | 3–6 mg bid | 12 | ||||
Parkinson’s disease dementia | 1.5–6 mg bid | 12 | |||||
Rivastigmine topical patch (Exelon Transdermal) | Alzheimer’s disease, mild to severe | 9.5–13.3 mg patch per 24 hours | 13.3 | ||||
Parkinson’s disease dementia | 9.5–13.3 mg patch per 24 hours | 13.3 | |||||
NMDA receptor antagonist | |||||||
Memantine (Namenda) | Alzheimer’s disease, moderate to severe | 10 mg bid | 20 | ||||
Memantine extended-release (Namenda XR) | Alzheimer’s disease, moderate to severe | 28 mg/day | 28 | ||||
Memantine/donepezil (Namzaric) | Alzheimer’s disease, moderate to severe | 28 mg/10 mg/ day† | 28/10 | †Patient stabilized on donepezil and not currently taking memantine: Start Namzaric 7 mg/ 10 mg once daily and increase by 7-mg increments of memantine every week up to maximum dosage of 28 mg/10 mg once daily. | |||
Monoclonal antibodies directed against aggregated forms of beta amyloid | |||||||
Aducanumab (Aduhelm) IV injection‡ | Alzheimer’s disease, patients with mild cognitive impairment (confirm presence of amyloid beta pathology prior to initiating treatment) | Refer to manufacturer's full prescribing information for administration guidelines and titration schedules. | — | ‡Warning: Amyloid-related imaging abnormalities (ARIAs)—Refer to manufacturer’s full prescribing information for complete boxed warning. | |||
Lecanemab (Leqembi) IV injection‡ | |||||||
AGENTS FOR TREATMENT OF MEDICATION-INDUCED MOVEMENT DISORDERS (EPS) | |||||||
Dopaminergic | |||||||
Amantadine | Medication-induced EPS | 100 mg bid | 300 | ||||
Amantadine extended-release (Gocovri) | Medication-induced EPS | 137–274 mg once daily at bedtime | 274 | ||||
Anticholinergics | |||||||
Benztropine (Cogentin) | Medication-induced EPS | 1–2 mg PO/IM bid–tid | 6 | Ages ≥ 3 years:* 0.02–0.05 mg/kg/day PO/IM (once daily or bid) | † | *Off-label use. †There are no well-established maximum dosages in children. | |
Benztropine mesylate injection (Cogentin Injection) | Acute dystonic reaction | 2 mg IM; repeat once after 30 minutes prn | † | †Usual maximum (standard practice) is 2 injections. | |||
Trihexyphenidyl | Medication-induced EPS | 5–15 mg/day (divided tid–qid) | 15 | ||||
Antihistaminic | |||||||
Diphenhydramine (Benadryl) | Medication-induced EPS | 25–50 mg PO/IM every 6–8 hours prn | 400 | Ages < 12 years: 1–2 mg/kg PO/IM every 6–8 hours prn | 50 mg/dose; 300 mg/day PO/IM | ||
Ages ≥ 12 years: 25–50 mg PO/IM every 6–8 hours prn | 100 mg/dose; 300 mg/day PO; 400 mg/day IM | ||||||
Acute dystonic reaction* | 50–100 mg IM/IV; repeat after 20–30 minutes prn | 100 mg/dose | Ages ≥ 6 years: 1–2 mg/kg/dose IM/IV; repeat after 20–30 minutes prn | 50 mg/dose | *Off-label use. | ||
Beta-adrenergic receptor antagonist | |||||||
Propranolol (Inderal) | Medication-induced akathisia* | 20–120 mg/day (divided tid–qid) | 120 | *Off-label use. | |||
Vesicular monoamine transporter 2 (VMAT2) inhibitors | |||||||
Deutetrabenazine (Austedo) | Chorea associated with Huntington’s disease Tardive dyskinesia | 6 mg once daily Gradually increase by 6 mg/day at weekly intervals. For total daily dosage of 12 mg or greater, administer as two divided doses | 48 | ||||
Valbenazine (Ingrezza) | Tardive dyskinesia Chorea associated with Huntington’s disease | 40 mg once daily After 1 week, increase to recommended dosage of 80 mg once daily | 80 | ||||
AGENTS FOR TREATMENT OF SUBSTANCE USE DISORDERS | |||||||
Acamprosate | Alcohol abstinence, maintenance | 666 mg tid | † | †There is no well-established acamprosate maximum dosage for the approved indication. | |||
Bupropion sustained-release (Zyban) | Smoking cessation | 150 mg bid | 300 | ||||
Disulfiram (Antabuse) | Alcohol abstinence | 125–500 mg/day in morning | 500 | ||||
Lofexidine (Lucemyra) | Opioid withdrawal symptoms | Three 0.18 mg tablets taken orally 4 times daily at 5- to 6-hour intervals. Treatment may be continued for up to 14 days with dosing guided by symptoms. | 2.88 (sixteen 0.18-mg tablets) | ||||
Naltrexone | Alcohol dependence | 50 mg/day | † | †There are no well-established naltrexone maximum dosages for the approved indications. | |||
Opioid dependence | Give 25 mg; if no withdrawal symptoms, start 50 mg/day | † | |||||
Naltrexone IM injection (Vivitrol) | Alcohol dependence | 380 mg IM every 4 weeks† | — | †Must not be actively drinking at time of first administration. | |||
Opioid dependence | 380 mg IM every 4 weeks† | — | †Must be opioid-free for 7–10 days. | ||||
AGENTS FOR TREATMENT OF SUBSTANCE USE DISORDERS (continued) | |||||||
Varenicline (Chantix) | Smoking cessation | Requires dosage titration† | 0.5 mg twice daily | †Refer to manufacturer's recommended dosing guidelines and titration schedules. |