Olanzapine Mabo 7.5 mg film-coated tablets EFG

Package leaflet: Information for the user

Introduction

PACKAGE LEAFLET: INFORMATION FOR THE USER

Olanzapina MABO 7.5 mg film-coated tablets EFG

Read the entire leaflet carefully before you start taking this medicine.

• Keep this leaflet, as you may need to read it again.
• If you have any questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you personally; do not give it to others, even if they have the same symptoms as you, as it may harm them.
• If you think any of the side effects you experience is serious or if you notice any side effects not listed in this leaflet, inform your doctor or pharmacist.

Leaflet contents:

1. What Olanzapina MABO 7.5 mg tablets are and what they are used for
2. Before you take Olanzapina MABO 7.5 mg tablets
3. How to take Olanzapina MABO 7.5 mg tablets
4. Possible side effects
5. How to store Olanzapina MABO 7.5 mg tablets
6. Further information

1. What OLANZAPINE MABO 7.5 mg TABLETS is and what it is used for

Olanzapine MABO tablets belong to a group of medicines called antipsychotics.

Olanzapine MABO is used to treat:

• a condition with symptoms such as hearing, seeing, or feeling things that are not real, false beliefs, unusual suspiciousness, and a tendency to withdraw socially. People with this condition may also feel depressed, anxious, or tense.

• a disorder characterized by symptoms such as feeling euphoric, having excessive energy, needing much less sleep than usual, speaking very rapidly with racing thoughts, and sometimes having considerable irritability. It is also a mood stabilizer that prevents the occurrence of extreme mood swings associated with this disorder.

2. BEFORE TAKING OLANZAPINE MABO 7.5 MG TABLETS

Do not take Olanzapine Mabo

• if you are allergic to olanzapine or to any of the other ingredients. The allergic reaction may manifest as rash, itching, swelling of the face or lips, or difficulty breathing. If this happens to you, tell your doctor immediately,
• if you have previously been diagnosed with narrow-angle glaucoma.

Take special care with Olanzapine Mabo

• medicines of this type may cause unusual movements, especially in the face or tongue. If this occurs after taking Olanzapine, inform your doctor,
• very rarely, medicines of this type may cause a combination of fever, rapid breathing, sweating, muscle rigidity, and mental confusion or drowsiness. If this occurs, stop taking the medication and contact your doctor immediately.

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

• diabetes
• heart disease
• liver or kidney disease
• Parkinson's disease
• epilepsy
• prostate problems
• intestinal blockage (paralytic ileus)
• blood disorders
• stroke or transient ischemic attack.

If you have dementia, you or your caregiver or family member should inform your doctor if you have ever had a stroke or transient ischemic attack.

If you or a family member has a history of blood clots, these medications may be associated with an increased risk of developing blood clots.

Children and adolescents under 18 years of age

Patients under 18 years of age must not take Olanzapine.

Elderly

The use of Olanzapine in elderly patients with dementia is not recommended, as it may cause serious adverse effects.

As a routine precaution, if you are over 65 years of age, your doctor should monitor your blood pressure.

Use of other medicines

Inform your doctor or pharmacist if you are taking or have recently taken any other medicines, including those obtained without a prescription.

Inform your doctor especially if you are taking medication for Parkinson's disease.

Only take other medicines together with Olanzapine if your doctor has authorized it. You may experience increased drowsiness if Olanzapine is combined with antidepressants or medicines for anxiety or sleep (tranquilizers).

You must inform your doctor if you are taking fluvoxamine (an antidepressant) or ciprofloxacin (an antibiotic), as your dose of Olanzapine may need to be adjusted.

Taking Olanzapine with food and drinks

Olanzapine Mabo tablets can be taken with or without food.

You must not drink alcohol during treatment with Olanzapine Mabo tablets. The combination of Olanzapine and alcohol may cause drowsiness.

Pregnancy and Breast-feeding

Consult your doctor or pharmacist before taking this medicine.

If you are pregnant or think you may be pregnant, consult your doctor before taking this medicine. You must not take this medicine during pregnancy unless your doctor specifically recommends it.

Newborns of mothers who have used Olanzapine Mabo during the third trimester of pregnancy may experience the following symptoms: tremors, muscle stiffness and/or weakness, drowsiness, agitation, breathing difficulties, and feeding problems. If your newborn shows any of these symptoms, contact your doctor immediately.

You must not take this medicine while breast-feeding, as small amounts of Olanzapine Mabo tablets may pass into breast milk.

Driving and use of machines

There is a risk of drowsiness while taking Olanzapine. If this occurs, do not drive or operate machinery. Discuss this with your doctor.

Important information about some of the components of Olanzapine Mabo

This medicine contains lactose. If your doctor has informed you that you have an intolerance to certain sugars, consult with him before taking this medicine.

This medicine contains soya oil. It must not be used if you are allergic to peanuts or soya.

3. HOW TO TAKE OLANZAPINE MABO 7.5 mg TABLETS

Follow exactly the administration instructions for OLANZAPINE MABO given by your doctor. If you have any doubts, consult your doctor or pharmacist.

The daily dose of Olanzapine ranges from 5 to 20 mg. Consult your doctor if your symptoms return, but do not stop taking Olanzapine unless your doctor tells you to.

Swallow the tablets whole with water.

Take your Olanzapine tablets once daily, as directed by your doctor. Try to take the tablets at the same time every day. Olanzapine tablets are for oral use.

Do not stop treatment when you feel better. It is very important that you continue taking Olanzapine for as long as your doctor advises.

If you take more Olanzapine MABO than you should

In case of overdose or accidental ingestion, contact your doctor or pharmacist immediately or call the Toxicology Information Service at: 91 562 04 20, stating the medication and the amount ingested. It is recommended to bring the medicine packaging and leaflet to the healthcare professional.

Patients who have taken more Olanzapine than recommended have experienced the following symptoms: rapid heartbeat, agitation/aggression, speech difficulties, unusual movements (especially of the face and tongue), and reduced level of consciousness. Other possible symptoms include: acute confusion, seizures (epilepsy), coma, a combination of fever, rapid breathing, sweating, muscle rigidity, drowsiness or lethargy, slowed breathing rate, aspiration, increased blood pressure or decreased blood pressure, and abnormal heart rhythms. Contact your doctor or go immediately to the hospital. Show the doctor the medicine pack and tablets.

If you forget to take Olanzapine MABO

If you forget to take a dose of Olanzapine, continue treatment with your next scheduled dose. Do not take a double dose to make up for a missed dose.

If you stop taking Olanzapine MABO

Do not stop treatment without first consulting your doctor, even if you feel better. Discontinuation of treatment should be done gradually and always under the doctor's instructions.

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

4. Possible adverse effects

Like all medicines, Olanzapine may cause adverse effects, although not everyone experiences them.

Uncommon side effects (may affect up to 1 in 100 people) include hypersensitivity (e.g. swelling of the mouth and throat, itching, skin rash); diabetes or worsening of diabetes, occasionally associated with ketoacidosis (acetone in blood and urine) or coma; seizures, which in most cases are related to a history of seizures (epilepsy); muscle rigidity or spasms (including eye movements); restless legs syndrome; speech problems; slow pulse; sensitivity to sunlight; nosebleeds; abdominal distension; memory loss or forgetfulness; urinary incontinence; inability to urinate; hair loss; absence or reduction of menstrual periods; and changes in the mammary gland in both men and women, such as abnormal production of breast milk or abnormal breast enlargement, and excessive salivation.

In this leaflet, when an adverse effect is described as "rare", it means it has been reported in more than 1 in 10,000 patients but in fewer than 1 in 1,000. When an adverse effect is described as "very rare", this means it has been reported in fewer than 1 in 10,000 patients.

Adverse effects of Olanzapine may include drowsiness or excessive fatigue, weight gain, dizziness, increased appetite, fluid retention, constipation, dry mouth, agitation, unusual movements (especially of the face or tongue), tremors, and changes in levels of certain blood cells and circulating fats. In some patients, very rarely, inflammation of the pancreas has developed, causing severe stomach pain, fever, and malaise.

Some people experience dizziness or fainting (with slower heartbeat) early in treatment, especially when getting up from a lying or sitting position. This sensation usually resolves spontaneously, but if it does not, inform your doctor.

Very rare cases of patients with abnormal heart rhythms, which may be serious, have been reported.

During treatment with Olanzapine, elderly patients with dementia may experience stroke, pneumonia, falls, extreme fatigue, visual hallucinations, elevated body temperature, skin redness, and difficulty walking. Some deaths have been reported in this particular group of patients.

Olanzapine may worsen symptoms in patients with Parkinson's disease.

Liver disorders have also been reported rarely. Very rarely, cases of prolonged and/or painful erection or difficulty urinating, decreased normal body temperature, blood clots (e.g., deep vein thrombosis in the legs), or muscle disorders presenting as unexplained muscle pains have been reported.

Very rarely, babies born to mothers who have taken Olanzapine during the last stage of pregnancy (third trimester) may experience tremors, drowsiness, or lethargy.

Blood clots in the veins, especially in the legs (symptoms include swelling, pain, and redness in the leg), may travel through blood vessels to the lungs, causing chest pain and difficulty breathing. If you experience any of these symptoms, contact your doctor immediately.

Serious allergic reactions have been reported, such as Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS). DRESS initially presents with flu-like symptoms, facial rash spreading to other areas, fever, swollen lymph nodes, elevated liver enzymes in blood tests, and increased levels of a type of white blood cell (eosinophilia).

Reporting of adverse effects:

If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if they are possible side effects not listed in this leaflet. You can also report them directly via the Spanish Pharmacovigilance System for Human Medicines (Website: www.notificaram.es). By reporting adverse effects, you can help provide more information on the safety of this medicine.

5. Storage of OLANZAPINE MABO 7.5 mg TABLETS

Keep out of the reach and sight of children.

Storage conditions:

No special storage conditions required.

Do not use Olanzapine MABO after the expiry date stated on the container. The expiry date refers to the last day of the month indicated.

Medicines should not be disposed of via wastewater or household waste. Return unused medicines and their containers to the SIGRE collection point at your pharmacy. If you are unsure, please ask your pharmacist how to properly dispose of unused medicines and their packaging. This will help protect the environment.

6. ADDITIONAL INFORMATION

Composition of Olanzapine MABO 7.5 mg tablets

• The active substance is olanzapine. Each film-coated tablet contains 7.5 mg of olanzapine.

• The other components (excipients) are: lactose, microcrystalline cellulose, crospovidone, magnesium stearate, polyvinyl alcohol, titanium dioxide E171, talc, soybean lecithin E322, xanthan gum E415.

Appearance of the medicinal product and contents of the container

Olanzapine MABO 7.5 mg is presented as film-coated tablets. The tablets are white, round and biconvex, with an imprint 'O2' on one side.

Pack sizes:

Al/Al blister packs containing 28 and 56 tablets.

Marketing Authorization Holder

MABO-FARMA S.A.

Calle Vía de los Poblados, 3,

Edificio 6, 28033 Madrid,

Spain

Manufacturer responsible

Actavis Ltd.

BLB016 Bulebel Industrial Estate

Zejtun ZTN 3000

Malta

This leaflet was last revised in May 2021

Detailed and up-to-date information on this medicinal product is available on the website of the Spanish Agency of Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/