Olanzapine is an atypical antipsychotic used to treat schizophrenia, bipolar I disorder (acute mania/mixed episodes and maintenance), and, in combination with fluoxetine, treatment‑resistant depression. It helps balance dopamine and serotonin to reduce hallucinations, delusions, severe mood swings, agitation, and insomnia associated with these conditions. Available as standard tablets, orally disintegrating tablets, short‑acting intramuscular injection for acute agitation, and, less commonly, a long‑acting injection, Olanzapine should be used under close medical supervision due to metabolic and neurologic risks. In the U.S., it is prescription‑only. Avoid trying to buy Olanzapine without prescription; instead, seek clinician‑guided care for safe, legal access and ongoing monitoring.
Olanzapine is an atypical antipsychotic indicated for schizophrenia and bipolar I disorder. In schizophrenia, it reduces positive symptoms (hallucinations, delusions, disorganized thinking) and can also improve negative symptoms (social withdrawal, flat affect). In bipolar I disorder, it treats acute manic or mixed episodes and helps with maintenance to reduce relapse risk, either alone or combined with mood stabilizers such as lithium or valproate.
In combination with fluoxetine, Olanzapine is also approved for treatment‑resistant depression and for bipolar depression. Short‑acting intramuscular Olanzapine is used in clinical settings for acute agitation associated with schizophrenia or bipolar mania. A long‑acting injectable (olanzapine pamoate) exists under a restricted program. Olanzapine is not approved for dementia‑related psychosis due to increased mortality risk in elderly patients with dementia.
Take Olanzapine exactly as prescribed, once daily, with or without food. Do not change your dose or stop suddenly without medical guidance. Tablets and orally disintegrating tablets (ODTs) are bioequivalent; allow ODTs to dissolve on the tongue without water if preferred. Avoid alcohol due to additive sedation.
Typical adult starting doses: for schizophrenia, 5–10 mg once daily, with a usual target of 10 mg/day (range 5–20 mg/day). For acute mania/mixed episodes in bipolar I, 10–15 mg once daily initially; maintenance doses often range from 5–20 mg/day. When used with lithium or valproate, 10 mg/day is common at initiation. For treatment‑resistant depression (with fluoxetine), fixed‑dose combinations are used; follow your clinician’s titration plan.
Dose adjustments are individualized based on response and tolerability. Start lower (e.g., 2.5–5 mg/day) in older adults, those with hepatic impairment, or patients sensitive to sedation/orthostasis, and titrate cautiously. Smokers may require higher doses due to CYP1A2 induction; conversely, strong CYP1A2 inhibitors (e.g., fluvoxamine) may necessitate dose reductions.
Short‑acting intramuscular Olanzapine is reserved for acute agitation in monitored settings. The long‑acting injection (olanzapine pamoate) has a specific monitoring program due to rare post‑injection sedation/delirium; it is administered only in qualified clinics. Your clinician will schedule regular follow‑ups to monitor efficacy, side effects, weight, glucose, and lipids.
Metabolic effects are central to Olanzapine’s risk profile. Significant weight gain, increased appetite, dyslipidemia, insulin resistance, and new‑onset diabetes can occur. Baseline and periodic checks of weight/BMI, waist circumference, fasting glucose/A1c, and lipid panel are recommended. Lifestyle support (diet, activity, sleep) should accompany therapy.
Other important precautions include sedation, dizziness, and orthostatic hypotension—use caution when driving or operating machinery and rise slowly from sitting. Extrapyramidal symptoms (restlessness/akathisia, tremor, rigidity) and tardive dyskinesia can occur, though rates are generally lower than with first‑generation antipsychotics. Rare but serious neuroleptic malignant syndrome (fever, rigidity, confusion, autonomic instability) requires emergency care. Olanzapine may elevate liver enzymes; periodic monitoring is prudent, especially with hepatic risk factors.
Olanzapine carries a boxed warning for increased mortality in elderly patients with dementia‑related psychosis and is not approved for this use. In pregnancy, antipsychotic exposure in the third trimester can cause neonatal extrapyramidal or withdrawal symptoms; discuss risks/benefits and birth‑planning. Olanzapine passes into breastmilk; monitor infants for sedation or feeding difficulties. Avoid dehydration and overheating; antipsychotics can impair temperature regulation. Seizure risk may increase, particularly in those with seizure history.
Olanzapine is contraindicated in patients with known hypersensitivity to Olanzapine or formulation components (e.g., prior severe rash, anaphylaxis, angioedema). It is not approved for dementia‑related psychosis due to increased risk of death and cerebrovascular events. Use extreme caution or alternative therapy in patients with severe hepatic impairment, significant anticholinergic burden (e.g., narrow‑angle glaucoma, urinary retention, severe constipation), or a history of leukopenia/neutropenia with antipsychotics.
Common side effects include somnolence, dizziness, dry mouth, increased appetite, weight gain, constipation, and orthostatic hypotension. Some individuals experience restlessness (akathisia) or mild tremor. Sexual dysfunction and modest prolactin elevations may occur but are typically less pronounced than with some other antipsychotics.
Metabolic issues (weight gain, elevated triglycerides/LDL, hyperglycemia) are dose‑related and may appear early; proactive lifestyle measures and monitoring help mitigate risks. Notify your clinician if you develop excessive thirst/urination, vision changes, or unexplained fatigue—possible signs of hyperglycemia. Injection‑related reactions (for long‑acting forms) include sedation/delirium syndrome rarely; hence mandatory observation in certified clinics.
Serious but uncommon events include neuroleptic malignant syndrome, severe neutropenia, pancreatitis, seizures, and allergic reactions (rash, swelling, difficulty breathing). Tardive dyskinesia (involuntary facial/tongue movements) can be persistent; risk increases with longer duration and cumulative dose, especially in older adults. If any severe or unusual symptoms occur, seek medical attention promptly.
Smoking (tobacco) induces CYP1A2 and can lower Olanzapine blood levels; quitting smoking can increase levels, potentially necessitating dose adjustment. Strong CYP1A2 inhibitors (e.g., fluvoxamine, ciprofloxacin) can markedly raise Olanzapine concentrations—dose reductions and close monitoring are recommended. Enzyme inducers such as carbamazepine or rifampin may reduce efficacy by lowering levels.
Additive CNS depression occurs with alcohol, opioids, benzodiazepines, sedative antihistamines, or sleep medications—combining can impair coordination and breathing. Concomitant parenteral benzodiazepines with intramuscular Olanzapine is specifically discouraged due to cardiorespiratory risk. Antihypertensives may have enhanced hypotensive effects; anticholinergic medications can intensify constipation, urinary retention, and dry mouth.
Olanzapine may antagonize dopamine agonists (e.g., levodopa) used in Parkinson’s disease, reducing their effectiveness. While Olanzapine has a relatively modest effect on QT interval compared with some antipsychotics, caution is prudent when combining with other QT‑prolonging agents or in patients with electrolyte abnormalities. Always provide a complete medication and supplement list to your clinician.
If you miss a dose, take it as soon as you remember unless it’s close to the time of your next dose. If it is, skip the missed dose and resume your regular schedule. Do not double up to “catch up.” If you frequently forget doses, ask your clinician about reminders, blister packs, or long‑acting injectable options.
Overdose symptoms may include profound drowsiness, agitation, confusion, slurred speech, tachycardia, hypotension, extrapyramidal symptoms, and, rarely, arrhythmias or seizures. Severe cases can progress to coma or neuroleptic malignant syndrome. Do not attempt to self‑treat.
Call emergency services or Poison Control (1‑800‑222‑1222 in the U.S.) immediately if an overdose is suspected. Supportive medical care is the mainstay; clinicians may use activated charcoal in a clinical setting and will monitor heart rhythm, breathing, and blood pressure. Avoid alcohol and sedatives, and do not drive.
Store Olanzapine tablets at room temperature (20–25°C/68–77°F), protected from moisture and light. Keep ODTs sealed in their blister until use; handle with dry hands. Secure all medications out of reach of children and pets. Use a medicine take‑back program for disposal; do not flush unless specifically instructed.
In the United States, Olanzapine is a prescription‑only medication. It is not legal or safe to buy Olanzapine without prescription. Purchasing antipsychotics from unverified sources risks counterfeit products, improper dosing, dangerous interactions, and lack of required monitoring for metabolic and neurologic side effects.
Geisinger HealthSouth provides a structured, lawful pathway to care: you can schedule an evaluation with a licensed clinician who will review your history, assess indications, discuss risks and benefits, and, if appropriate, issue a legitimate prescription that can be filled at a licensed pharmacy. They do not dispense Olanzapine without a prescription; instead, they streamline access to evidence‑based treatment, monitoring, and follow‑up.
For your protection, avoid online offers that claim to sell “Olanzapine without prescription.” Use accredited pharmacies and verify telehealth services. If cost is a barrier, ask about generics, insurance coverage, patient assistance, or pharmacy discount programs. Proper medical oversight ensures safer dosing, lab monitoring (weight, glucose, lipids), and timely adjustments to optimize outcomes.
Olanzapine is an atypical antipsychotic used to treat schizophrenia and bipolar I disorder (manic or mixed episodes, maintenance). In combination with fluoxetine, it is used for treatment-resistant major depression and bipolar depression. It may also be used off-label for chemotherapy-related nausea, severe agitation, and other conditions at a clinician’s discretion.
Olanzapine blocks dopamine D2 and serotonin 5-HT2A receptors, helping rebalance neurotransmission involved in psychosis and mood symptoms. It also affects other receptors (histamine, muscarinic, alpha-adrenergic), which contributes to benefits and side effects such as sedation and dry mouth.
Some calming and sleep benefits may appear within days. Psychotic and manic symptoms often improve within 1–2 weeks, with continued gains over 4–6 weeks. Depressive symptoms with the olanzapine/fluoxetine combination may improve in 1–2 weeks but can take longer.
Common effects include sleepiness, increased appetite, weight gain, dry mouth, constipation, dizziness, and orthostatic lightheadedness. Some people experience edema, increased cholesterol and triglycerides, and elevated blood sugar.
Serious risks include metabolic syndrome (weight gain, diabetes, dyslipidemia), neuroleptic malignant syndrome (rare), tardive dyskinesia, severe orthostatic hypotension, high blood sugar leading to ketoacidosis (rare), liver enzyme elevation, and blood problems (rare neutropenia). Elderly patients with dementia-related psychosis have an increased risk of death.
Yes, olanzapine is among the antipsychotics most associated with weight gain and increased appetite. Risk can be mitigated with early lifestyle measures (dietary counseling, physical activity), regular weight and waist monitoring, managing sleep, and, when appropriate, considering adjuncts such as metformin after clinician evaluation.
Typical adult starting doses are 5–10 mg daily for schizophrenia and 10–15 mg daily for acute mania, usually taken once daily. The usual effective range is 10–20 mg/day. Doses are individualized based on response and tolerability. For bipolar depression or treatment-resistant depression, olanzapine is paired with fluoxetine at fixed-dose combinations.
Yes, sedation is common due to histamine receptor blockade. Many people take it at bedtime to reduce daytime drowsiness. If daytime sedation persists, speak with your clinician about dose adjustments or timing.
Monitor weight, BMI, waist circumference, blood pressure, fasting glucose or A1c, and lipid panel at baseline and periodically. Clinicians also assess for movement disorders (AIMS exam), sedation, orthostatic symptoms, and signs of high blood sugar. Liver enzymes may be checked if indicated.
Use during pregnancy is a risk–benefit decision. Late-pregnancy exposure can cause transient neonatal symptoms (jitteriness, feeding difficulties). Olanzapine passes into breast milk; infant exposure is usually low but monitor for sedation or poor feeding. Always discuss with a clinician specializing in perinatal psychiatry.
Olanzapine can be used cautiously in older adults, but it carries a boxed warning for increased mortality in elderly patients with dementia-related psychosis and is not approved for that use. Lower starting doses and close monitoring for orthostatic hypotension, sedation, and metabolic changes are prudent.
Yes. Smoking induces CYP1A2 and can lower olanzapine levels, while strong CYP1A2 inhibitors (e.g., fluvoxamine, ciprofloxacin) can increase levels. Carbamazepine can reduce levels. Alcohol and other sedatives can worsen drowsiness. Avoid combining intramuscular olanzapine with parenteral benzodiazepines due to respiratory depression risk.
Take it when you remember unless it’s close to your next dose; if so, skip the missed dose. Do not double up. If you miss multiple doses, contact your prescriber, as a gradual retitration may be needed to minimize side effects.
Do not stop abruptly unless medically necessary. A gradual taper over weeks helps reduce relapse risk and cholinergic rebound symptoms (insomnia, agitation, nausea). Your clinician will tailor a schedule based on dose, duration, and clinical status.
Olanzapine is available as standard tablets, orally disintegrating tablets (ODT), a short-acting intramuscular injection for acute agitation, and a long-acting injectable (olanzapine pamoate) that requires post-injection observation due to rare post-injection delirium/sedation syndrome.
Yes, for treatment-resistant major depression and bipolar depression, olanzapine is combined with fluoxetine. This combination can be effective but carries a higher risk of weight gain and metabolic side effects, so monitoring is essential.
Both are effective for schizophrenia and mania. Olanzapine tends to cause more weight gain and metabolic issues, while risperidone has a higher risk of prolactin elevation and extrapyramidal symptoms (EPS) at higher doses. Choice often depends on side-effect priorities and individual response.
Olanzapine is often more potent for acute mania and psychosis, but quetiapine is approved for bipolar depression monotherapy and is generally preferred there. Quetiapine can cause sedation and hypotension; olanzapine causes more weight and metabolic changes. Both may cause sedation.
Olanzapine is more sedating and carries higher metabolic risk. Aripiprazole is more activating, has lower weight gain risk, and can cause akathisia (inner restlessness). For patients prone to metabolic issues, aripiprazole is often favored; for severe agitation, olanzapine’s sedation can be useful short term.
Clozapine is reserved for treatment-resistant schizophrenia due to superior efficacy but requires blood monitoring for agranulocytosis and has significant metabolic and anticholinergic effects. Olanzapine lacks mandatory blood monitoring and has fewer rare hematologic risks but still has high metabolic burden.
Olanzapine has higher efficacy for some patients but greater weight and lipid/glucose effects. Ziprasidone is weight-neutral for many and has a lower metabolic risk but can prolong the QT interval and must be taken with food for absorption. Sedation is usually less with ziprasidone.
Olanzapine is more sedating and more likely to cause weight gain and dyslipidemia. Lurasidone tends to be metabolically friendlier, is approved for bipolar depression, and must be taken with food. Lurasidone may cause akathisia; olanzapine less so but causes more sedation.
Olanzapine causes more metabolic side effects; paliperidone more often elevates prolactin and can cause EPS at higher doses. Long-acting injectable options exist for both (different products and schedules). Choice depends on tolerability, need for LAI, and specific symptom profile.
Olanzapine generally causes fewer EPS and tardive dyskinesia than haloperidol but more weight gain and metabolic effects. For acute agitation, both can be effective; olanzapine is more sedating, haloperidol is less metabolically problematic but carries higher motor side-effect risk.
Olanzapine is more associated with weight gain and sedation. Asenapine (sublingual) has lower metabolic risk but can cause oral numbness and taste changes. Both are effective in acute mania; olanzapine may be preferred for severe agitation, asenapine for patients sensitive to weight gain.
Olanzapine is sedating and metabolically heavy; cariprazine (a D3/D2 partial agonist) has a lower metabolic burden and is notable for efficacy in negative symptoms and bipolar depression, but can cause akathisia and insomnia. Onset for cariprazine can be slower due to long half-life.
Olanzapine often provides robust antimanic and antipsychotic effects with more sedation and weight gain. Brexpiprazole tends to be better tolerated metabolically, with lower akathisia rates than aripiprazole, but may be less sedating. Brexpiprazole is used in schizophrenia and as an adjunct in major depression.
Quetiapine is a first-line monotherapy for bipolar depression with supportive evidence across doses. Olanzapine alone is less favored for bipolar depression, but the olanzapine/fluoxetine combination is effective. Metabolic risk is higher with olanzapine-containing regimens.
Olanzapine generally has minimal impact on prolactin compared with risperidone and paliperidone, which often elevate prolactin and can cause sexual dysfunction, menstrual changes, or galactorrhea. If prolactin elevation is a concern, olanzapine may be preferable despite metabolic risks.
Olanzapine has a relatively low QT prolongation risk. Ziprasidone prolongs QT more and should be used cautiously in patients with cardiac risk factors or on other QT-prolonging drugs. Conversely, ziprasidone is more favorable metabolically than olanzapine.
Olanzapine rarely causes akathisia and is sedating. Aripiprazole more commonly causes akathisia and can be activating or cause insomnia, though it is metabolically sparing. Patient preference and sensitivity to restlessness often guide the choice.
Olanzapine has one of the highest risks for weight gain, hyperlipidemia, and hyperglycemia. Lurasidone is typically weight-neutral and has a better metabolic profile, making it attractive for patients with diabetes or cardiovascular risk, provided it is tolerated and effective for symptoms.