OLANZAPINE TEVA 10 MG FILM-COATED TABLETS - patient leaflet, side effects, dosage

What Olanzapine Teva is and what it is used for

Olanzapine Teva contains the active substance olanzapine. Olanzapine Teva belongs to a group of medicines called antipsychotics and is used to treat the following conditions:

• – Schizophrenia, a disease with symptoms such as hearing, seeing or sensing things which are not there, mistaken beliefs, unusual suspiciousness, and becoming withdrawn. People with this disease may also feel depressed, anxious or tense.

• – Moderate to severe manic episodes, a condition with symptoms of excitement or euphoria.

Olanzapine Teva has been shown to prevent recurrence of these symptoms in patients with bipolar disorder whose manic episode has responded to olanzapine treatment.

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What you need to know before you take Olanzapine Teva

Do not take Olanzapine Teva

• – if you are allergic to olanzapine or any of the other ingredients of this medicine (listed in section 6). An allergic reaction may be recognised as a rash, itching, a swollen face, swollen lips or shortness of breath. If this has happened to you, tell your doctor.

• – if you have been previously diagnosed with eye problems such as certain kinds of glaucoma (increased pressure in the eye).

Warnings and precautions

Talk to your doctor or pharmacist before taking Olanzapine Teva.

• – The use of Olanzapine Teva in elderly patients with dementia is not recommended as it may have serious side effects.

• – Medicines of this type may cause unusual movements mainly of the face or tongue. If this happens after you have been given Olanzapine Teva tell your doctor.

• – Very rarely, medicines of this type cause a combination of fever, faster breathing, sweating, muscle stiffness and drowsiness or sleepiness. If this happens, contact your doctor at once.

• – Weight gain has been seen in patients taking Olanzapine Teva. You and your doctor should check your weight regularly. Consider referral to a dietician or help with a diet plan if necessary.

• – High blood sugar and high levels of fat (triglycerides and cholesterol) have been seen in patients taking Olanzapine Teva. Your doctor should do blood tests to check blood sugar and certain fat levels before you start taking Olanzapine Teva and regularly during treatment.

• – Tell the doctor if you or someone else in your family has a history of blood clots, as medicines like these have been associated with the formation of blood clots.

If you suffer from any of the following illnesses tell your doctor as soon as possible:

• – Stroke or “mini” stroke (temporary symptoms of stroke)

• – Parkinson’s disease

• – Prostate problems

• – A blocked intestine (Paralytic ileus)

• – Liver or kidney disease

• – Blood disorders

• – Heart disease

• – Diabetes

• – Seizures

• – If you know that you may have salt depletion as a result of prolonged severe diarrhoea and vomiting (being sick) or usage of diuretics (water tablets)

If you suffer from dementia, you or your carer/relative should tell your doctor if you have ever had a stroke or “mini” stroke.

As a routine precaution, if you are over 65 years your blood pressure may be monitored by your doctor.

Children and adolescents

Olanzapine Teva is not for patients who are under 18 years.

Other medicines and Olanzapine Teva

Tell your doctor or pharmacist if you are taking, have recently taken or might take use any other medicines.

Only take other medicines while you are on Olanzapine Teva if your doctor tells you that you can. You might feel drowsy if Olanzapine Teva is taken in combination with antidepressants or medicines taken for anxiety or to help you sleep (tranquillisers).

In particular, tell your doctor if you are taking: – medicines for Parkinson’s di­sease.

• – carbamazepine (an anti-epileptic and mood stabiliser), fluvoxamine (an antidepressant) or ciprofloxacin (an antibiotic) – it may be necessary to change your Olanzapine Teva dose.

Olanzapine Teva with alcohol

Do not drink any alcohol if you have been given Olanzapine Teva as together with alcohol it may make you feel drowsy.

Pregnancy and breast-feeding

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.

You should not be given this medicine when breast-feeding, as small amounts of Olanzapine Teva can pass into breast milk.

The following symptoms may occur in newborn babies, of mothers that have used Olanzapine Teva in the last trimester (last three months of their pregnancy): shaking, muscle stiffness and/or weakness, sleepiness, agitation, breathing problems, and difficulty in feeding. If your baby develops any of these symptoms you may need to contact your doctor.

Driving and using machines

There is a risk of feeling drowsy when you are given Olanzapine Teva. If this happens do not drive or operate any tools or machines. Tell your doctor.

Olanzapine Teva contains lactose

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

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Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

Your doctor will tell you how many Olanzapine Teva tablets to take and how long you should continue to take them. The daily dose of Olanzapine Teva is between 5 mg and 20 mg. Consult your doctor if your symptoms return but do not stop taking Olanzapine Teva unless your doctor tells you to.

You should take your Olanzapine Teva tablets once a day following the advice of your doctor. Try to take your tablets at the same time each day. It does not matter whether you take them with or without food. Olanzapine Teva coated tablets are for oral use. You should swallow the Olanzapine Teva tablets whole with water.

If you take more Olanzapine Teva than you should Patients who have taken more Olanzapine Teva than they should have experienced the following symptoms: rapid beating of the heart, agitation/aggres­siveness, problems with speech, unusual movements (especially of the face or tongue) and reduced level of consciousness. Other symptoms may be: acute confusion, seizures (epilepsy), coma, a combination of fever, faster breathing, sweating, muscle stiffness and drowsiness or sleepiness, slowing of the breathing rate, aspiration, high blood pressure or low blood pressure, abnormal rhythms of the heart. Contact your doctor or hospital straight away if you experience any of the above symptoms. Show the doctor your pack of tablets.

If you forget to take Olanzapine Teva

Take your tablets as soon as you remember. Do not take two doses in one day.

If you stop taking Olanzapine Teva

Do not stop taking your tablets just because you feel better. It is important that you carry on taking Olanzapine Teva for as long as your doctor tells you. If you suddenly stop taking Olanzapine Teva, symptoms such as sweating, unable to sleep, tremor, anxiety or nausea and vomiting might occur. Your doctor may suggest you to reduce the dose gradually before stopping treatment.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Tell your doctor immediately if you have:

• – unusual movement (a common side effect that may affect up to 1 in 10 people) mainly of the face or tongue;

• – blood clots in the veins (an uncommon side effect that may affect up to 1 in 100 people) especially in the legs (symptoms include swelling, pain, and redness in the leg), which may travel through blood vessels to the lungs causing chest pain and difficulty in breathing. If you notice any of these symptoms seek medical advice immediately;

• – a combination of fever, faster breathing, sweating, muscle stiffness and drowsiness or sleepiness (the frequency of this side effect cannot be estimated from the available data).

Very common side effects (may affect more than 1 in 10 people) include weight gain; sleepiness; and increases in levels of prolactin in the blood. In the early stages of treatment, some people may feel dizzy or faint (with a slow heart rate), especially when getting up from a lying or sitting position. This will usually pass on its own but if it does not, tell your doctor.

Common side effects (may affect up to 1 in 10 people) include changes in the levels of some blood cells, circulating fats and early in treatment, temporary increases in liver enzymes; increases in the level of sugars in the blood and urine; increases in levels of uric acid and creatine phosphokinase in the blood; feeling more hungry; dizziness; restlessness; tremor; unusual movements (dyskinesias); constipation; dry mouth; rash; loss of strength; extreme tiredness; water retention leading to swelling of the hands, ankles or feet; fever; joint pain; and sexual dysfunctions such as decreased libido in males and females or erectile dysfunction in males

Uncommon side effects (may affect up to 1 in 100 people) include hypersensitivity (e.g. swelling in the mouth and throat, itching, rash); diabetes or the worsening of diabetes, occasionally associated with ketoacidosis (ketones in the blood and urine) or coma; seizures, usually associated with a history of seizures (epilepsy); muscle stiffness or spasms (including eye movements); restless legs syndrome; problems with speech; stuttering; slow heart rate; sensitivity to sunlight; bleeding from the nose; abdominal distension; drooling; memory loss or forgetfulness; urinary incontinence; lack of ability to urinate; hair loss; absence or decrease in menstrual periods; and changes in breasts in males and females such as an abnormal production of breast milk or abnormal growth.

Rare side effects (may affect up to 1 in 1000 people) include lowering of normal body temperature; abnormal rhythms of the heart; sudden unexplained death; inflammation of the pancreas causing severe stomach pain, fever and sickness; liver disease appearing as yellowing of the skin and white parts of the eyes; muscle disease presenting as unexplained aches and pains; and prolonged and/or painful erection.

Very rare side effects include serious allergic reactions such as Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS). DRESS appears initially as flu like symptoms with a rash on the face and then with an extended rash, high temperature, enlarged lymph nodes, increased levels of liver enzymes seen in blood tests and an increase in a type of white blood cell (eosinophilia). While taking olanzapine, elderly patients with dementia may suffer from stroke, pneumonia, urinary incontinence, falls, extreme tiredness, visual hallucinations, a rise in body temperature, redness of the skin and have trouble walking. Some fatal cases have been reported in this particular group of patients.

In patients with Parkinson's disease Olanzapine Teva may worsen the symptoms.

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme Website: or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

How to store Olanzapine Teva

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month.

Do not store above 25°C. Store in the original package in order to protect from light.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

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Contents of the pack and other information

What Olanzapine Teva contains

• – The active substance is olanzapine.

Each Olanzapine Teva 2.5 mg film-coated tablet contains 2.5 mg of the active substance.

Each Olanzapine Teva 5 mg film-coated tablet contains 5 mg of the active substance.

Each Olanzapine Teva 7.5 mg film-coated tablet contains 7.5 mg of the active substance.

Each Olanzapine Teva 10 mg film-coated tablet contains 10 mg of the active substance.

Each Olanzapine Teva 15 mg film-coated tablet contains 15 mg of the active substance.

Each Olanzapine Teva 20 mg film-coated tablet contains 20 mg of the active substance.

• – The other ingredients are:

What Olanzapine Teva looks like and contents of the pack

Olanzapine Teva 2.5 mg film-coated tablet is a white, biconvex, round film-coated tablet, debossed “OL 2.5” on one side and plain on the other. Olanzapine Teva 5 mg film-coated tablet is a white, biconvex, round film-coated tablet, debossed “OL 5” on one side and plain on the other.

Olanzapine Teva 7.5 mg film-coated tablet is a white, biconvex, round film-coated tablet, debossed “OL 7.5” on one side and plain on the other.

Olanzapine Teva 10 mg film-coated tablet is a white, biconvex, round film-coated tablet, debossed “OL 10” on one side and plain on the other.

Olanzapine Teva 15 mg film-coated tablet is a light blue, biconvex, oval film-coated tablet, debossed “OL 15” on one side and plain on the other. Olanzapine Teva 20 mg film-coated tablet is a pink, biconvex, oval film-coated tablet, debossed “OL 20” on one side and plain on the other.

Olanzapine Teva 2.5 mg film-coated tablets are available in cartons of 28, 30, 35, 56, 70 or 98 film-coated tablets.

Olanzapine Teva 5 mg film-coated tablets are available in cartons of 28, 28 × 1, 30, 30 × 1, 35, 35 × 1, 50, 50 × 1, 56, 56 × 1, 70, 70 × 1, 98 or 98 × 1 film-coated tablets.

Olanzapine Teva 7.5 mg film-coated tablets are available in cartons of 28, 28 × 1, 30, 30 × 1, 35, 35 × 1, 56, 56 × 1, 60, 70, 70 × 1, 98 or 98 × 1 film-coated tablets.

Olanzapine Teva 10 mg film-coated tablets are available in cartons of 7, 7 × 1, 28, 28 × 1, 30, 30 × 1, 35, 35 × 1, 50, 50 × 1, 56, 56 × 1, 60, 70, 70 × 1, 98 or 98 x1 film-coated tablets.

Olanzapine Teva 15 mg film-coated tablets are available in cartons of 28, 30, 35, 50, 56, 70 or 98 film-coated tablets.

Olanzapine Teva 20 mg film-coated tablets are available in cartons of 28, 30, 35, 56, 70 or 98 film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Teva B.V.

Swensweg 5

2031GA Haarlem

The Netherlands

Manufacturer

Teva Pharmaceutical Works

Pallagi ut 13

4042 Debrecen

Hungary

For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:

Belgie/Belgiqu­e/Belgien

Teva Pharma Belgium N.V./S.A./AG

Tel/Tel: +32 38207373

Bbnrapun

Aktobuc EAfl

Ten.: +359 24899585

C eska republika

Teva Pharmaceuticals CR, s.r.o.

Tel: +420 251007111

Danmark

SanoSwiss UAB

Litauen

Tlf: +370 70001320

Deutschland

Teva GmbH

Tel: +49 73140208

Eesti

UAB Teva Baltics Eesti filiaal

Tel: +372 6610801

EAAa6a

Teva EAAa^ A.E.

TnA: +30 2118805000

Espana

Teva Pharma, S.L.U.

Tel: +34 913873280

France

Teva Sante

Tel: +33 155917800

Hrvatska

Pliva Hrvatska d.o.o.

Tel: +385 13720000

Ireland

Teva Pharmaceuticals Ireland

Tel: +353 19127700

Island

Actavis Pharmaceuticals Iceland ehf.

Simi: +354 5503300

Italia

Teva Italia S.r.l.

Tel: +39 028917981

Kunpoc

Teva EAAa^ A.E.

EAAaSa

TnA: +30 2118805000

Latvija

UAB Teva Baltics filiale Latvija

Tel: +371 67323666

Lietuva

UAB Teva Baltics

Tel: +370 52660203

Luxembourg/Lu­xemburg

Teva Pharma Belgium N.V./S.A./AG Belgique/Belgien

Tel/Tel: +32 38207373

Magyarorszag

Teva Gyogyszergyar Zrt.

Tel: +36 12886400

Malta

Teva Pharmaceuticals Ireland

L-Irlanda

Tel: +353 19127700

Nederland

Teva Nederland B.V.

Tel: +31 8000228400

Norge

Teva Sweden AB

Sverige

Tlf: +46 42121100

Osterreich

ratiopharm Arzneimittel Vertriebs GmbH

Tel: +43 1970070

Polska

Teva Pharmaceuticals Polska Sp. z o.o

Tel: +48 223459300

Portugal

Teva Pharma – Produtos Farmaceuticos Lda.

Tel: +351 214767550

Romania

Teva Pharmaceuticals S.R.L.

Tel: +40 212306524

Slovenija

Pliva Ljubljana d.o.o.

Tel: +386 15890390

Slovenska republika

Teva Pharmaceuticals Slovakia s.r.o.

Tel: +421 257267911

Suomi/Finland

Teva Finland Oy

Puh/Tel: +358 201805900

Sverige

Teva Sweden AB

Tel: +46 42121100

United Kingdom

Teva UK Limited

Tel: +44 1977628500

This leaflet was last revised in 04/2020.

Detailed information on this medicine is available on the European Medicines Agency web site:.

TEVA UK LIMITED EAS2402e

REG0183502

Version 9.0

Effective

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