Quetiapina pensa 150 mg comprimidos de liberacion prolongada efg

Leaflet:information for the user

Quetiapine pensa 150 mg prolonged-release tablets EFG

Read this leaflet carefully before you start taking this medicine,because it contains important information for you.

• Keep this leaflet, as you may need to read it again.
• If you have any questions, ask yourdoctor orpharmacist.

-This medicine has been prescribed for you only.Do not give it to others even if they have the same symptoms as you,as it may harm them.

• If you experience any side effects,consult your doctor or pharmacist,even if they are not listed in this leaflet. See section 4.

1.What Quetiapine pensa is and what it is used for

2.What you need to know before you start taking Quetiapine pensa

3.How to take Quetiapine pensa

4.Possible side effects

5Storage of Quetiapine pensa

6.Contents of the pack and additional information

This medication contains a substance called quetiapina. It belongs to a group of medications called antipsicotics. This medication may be used to treat several diseases, such as:

• Bipolar depression and major depressive episodes in major depressive disorder: for which you may feel sad. You may find that you feel depressed, guilty, lack energy, lose your appetite, or cannot sleep.
• Mania: for which you may feel very excited, euphoric, agitated, enthusiastic, or hyperactive, or present poor judgment, which includes being aggressive or violent.
• Schizophrenia: for which you may hear or feel things that are not there, believe things that are not true, or feel abnormally suspicious, anxious, confused, guilty, tense, or depressed.

When using this medication to treat major depressive episodes in major depressive disorder, it will be taken in addition to another medication that is being used to treat this disease.

Your doctor may continue prescribing this medication even when you are feeling better.

Do not take Quetiapina if you think:

- you are allergic to quetiapina or any of the other ingredients in this medicine (listed in section 6)

- you are taking any of the following medicines:

- Some medicines for HIV

- Medicines of the azole type (for fungal infections)

- Erythromycin or clarithromycin (for infections)

- Nefazodone (for depression)

If you are unsure, consult your doctor or pharmacist before taking this medicine.

Warnings and precautions

Consult your doctor or pharmacist before starting to take quetiapina:

- if you, or a family member, have or have had any heart problems, for example, irregular heart rhythm, weakening of the heart muscle, or inflammation of the heart, or if you are taking any medicine that may affect your heart rhythm.

- if you have low blood pressure.

- if you have had a stroke, especially if you are elderly.

- if you have liver problems.

- if you have ever had a seizure (convulsion).

- if you have diabetes or are at risk of developing diabetes. Your doctor may monitor your blood sugar levels while you are taking this medicine.

- if you know you have had low white blood cell counts (which may or may not have been caused by other medicines).

- if you are an elderly person with dementia (loss of brain function). If so, do not take quetiapina because the group of medicines to which quetiapina belongs may increase the risk of stroke, or in some cases the risk of death, in these people.

- if you are an elderly person with Parkinson's disease/parkinsonism.

- if you or a family member has a history of blood clots, as medicines like these have been associated with the formation of blood clots.

- if you have or have had a condition in which your breathing is interrupted by short periods of time during normal sleep at night (called "sleep apnea") and are taking medicines that decrease the normal activity of the brain ("depressants").

- if you have or have had a condition in which you cannot completely empty your bladder (urinary retention), have an enlarged prostate, a blockage in your intestine, or high pressure inside your eye. These conditions may be caused by medicines (called "anticholinergics") that affect the way nerve cells work, to treat certain medical conditions.

- if you have a history of alcohol or drug abuse.

- If you have depression or other conditions that are treated with antidepressants. The use of these medicines with quetiapina may cause serotonin syndrome, a potentially life-threatening condition (see "Other medicines and Quetiapina pensa").

Inform your doctor immediately if after taking quetiapina you experience any of the following:

- A combination of fever, intense muscle stiffness, sweating, or a decrease in level of consciousness (a condition called "neuroleptic malignant syndrome"). You may need immediate medical treatment.

- Uncontrolled movements, mainly of your face or tongue.

- Dizziness or feels very drowsy. This may increase the risk of accidental injuries (falls) in elderly patients.

- Seizures (convulsions).

- A prolonged and painful erection (priapism).

- Rapid and irregular heartbeats, even when at rest, palpitations, respiratory problems, chest pain, or unexplained fatigue. Your doctor should examine your heart and, if necessary, refer you to a cardiologist immediately.

These conditions may be caused by this type of medicine.

Inform your doctor as soon as possible if you have:

- Fever, flu-like symptoms, sore throat, or any other infection, as it may be a consequence of a very low white blood cell count and may require discontinuation of quetiapina treatment and/or additional treatment.

- Constipation with persistent abdominal pain, or constipation that has not responded to treatment, as it may lead to a more severe intestinal blockage.

-Thoughts of suicide and worsening of depression

If you are depressed, you may sometimes think about harming yourself or committing suicide. This may increase at the beginning of treatment, as all these medicines take time to become effective, usually around two weeks but sometimes longer. These thoughts may also increase if you stop taking your medication abruptly. You may be more likely to think this way if you are a young adult. Information from clinical trials has shown an increased risk of thoughts of suicide and/or suicidal behavior in young adults under 25 with depression.

If you ever think about harming yourself or committing suicide, contact your doctor or go to a hospital immediately. It may help to tell a close family member or friend that you are depressed, and ask them to read this leaflet. You may ask them to tell you if they think your depression is getting worse, or if they are concerned about changes in your behavior.

- Erythema multiforme with eosinophilia and systemic symptoms (DRESS, for its English acronym). Generalized rash, elevated body temperature, elevated liver enzymes, blood abnormalities (eosinophilia), enlarged lymph nodes, and other organs involved (erythema multiforme with eosinophilia and systemic symptoms, also known as DRESS).

If you develop these symptoms, stop using quetiapina and contact your doctor or seek medical attention immediately.

Weight gain

Weight gain has been observed in patients taking quetiapina. You and your doctor should monitor your weight regularly.

Children and adolescents

Quetiapina should not be used in children and adolescents under 18 years of age.

Other medicines and Quetiapina pensa

Inform your doctor if you are taking, have taken recently, or may need to take any other medicine.

Do not take this medicine if you are using any of the following medicines:

- Some medicines for HIV.

- Medicines of the azole type (for fungal infections).

- Erythromycin or clarithromycin (for infections).

- Nefazodone (for depression).

Inform your doctor if you are using any of the following medicines:

- Medicines for epilepsy (such as phenytoin or carbamazepine).

- Medicines for high blood pressure.

- Barbiturates (for difficulty falling asleep).

- Thioridazine or Lithium (other antipsychotic medicines).

- Medicines that affect your heart rhythm, for example, medicines that may cause an imbalance of electrolytes (low potassium or magnesium) such as diuretics (medicines for urination) or certain antibiotics (medicines for treating infections).

- Medicines that may cause constipation.

- Medicines (called "anticholinergics") that affect the way nerve cells work, to treat certain medical conditions.

- Antidepressants. These medicines may interact with quetiapina and you may experience symptoms such as involuntary and rhythmic muscle contractions, including those that control eye movement, agitation, hallucinations, coma, excessive sweating, tremor, exaggerated reflexes, increased muscle tension, and body temperature above 38 °C (serotonin syndrome). Contact your doctor when you experience these symptoms.

Before stopping any of your medicines, consult your doctor first.

Quetiapina pensa with food, drinks, and alcohol

- Quetiapina may be affected by food, so take your tablets at least one hour before a meal or before bedtime.

- Be careful with the amount of alcohol you drink. This is because the combined effect of quetiapina and alcohol may make you drowsy.

- Do not take orange juice while taking this medicine. It may affect the way the medicine works.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, or think you may be pregnant, or plan to become pregnant, consult your doctor before using this medicine. Do not take quetiapina during pregnancy, unless your doctor has advised you to. Do not use quetiapina if you are breastfeeding.

The following symptoms, which may represent withdrawal syndrome, may appear in newborn babies of mothers who have used this medicine in the last trimester (last three months of their pregnancy): tremor, muscle stiffness, and/or weakness, drowsiness, agitation, respiratory problems, and difficulty feeding. If your newborn develops any of these symptoms, you may need to contact your doctor.

Driving and operating machinery

These tablets may make you feel drowsy. Do not drive or operate tools or machinery until you know how the tablets affect you.

Quetiapina pensa contains lactose

If your doctor has told you that you have an intolerance to certain sugars, consult with him before starting to take this medicine.

Effect on Drug Detection Tests in Urine

If you are having a drug detection test in urine, taking this medicine may produce positive results for methadone or certain antidepressant medicines called tricyclic antidepressants (TCAs) when using some analysis methods, although you may not be taking methadone or TCAs. If this occurs, a more specific test may be performed.

Follow exactly the administration instructions of this medication as indicated by your doctor or pharmacist.In case of doubt, consult your doctor or pharmacist again.

Your doctor will decide your initial dose. The maintenance dose (daily dose) will depend on your illness and your needs, but it will usually be between 150 mg and 800 mg.

- You will take your tablets once a day.

- Do not break, chew, or crush the tablets.

- Swallow your tablets whole with the help of water.

- Take the tablets without food (at least one hour before a meal or before going to bed, your doctor will tell you when).

- Do not take grapefruit juice while taking this medication. It may affect how the medication works.

- Do not stop taking your tablets even if you feel better, unless your doctor tells you to.

Liver problems

If you have liver problems, your doctor may change your dose.

Older adults

If you are an older adult, your doctor may change your dose.

Use in children and adolescents

Quetiapina pensa should not be used in children and adolescents under 18 years of age.

If you take more Quetiapina pensa than you should

If you take more quetiapina than your doctor prescribed, you may feel drowsy, feel dizzy, and experience abnormal heartbeats. Contact your doctor or the nearest hospital immediately. Bring the tablets of this medication with you. You can also call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount taken.

If you forget to take Quetiapina pensa

If you forget to take a dose, take it as soon as you remember. If it is almost time to take the next dose, wait until then. Do not take a double dose to make up for the missed tablet.

If you interrupt the treatment with Quetiapina pensa

If you stop taking quetiapina abruptly, you may be unable to sleep (insomnia), or you may feel nausea, or you may experience headaches, diarrhea, vomiting, dizziness, or irritability. Your doctor may suggest reducing the dose gradually before stopping treatment.

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

Like all medicines, this medicine can cause side effects, although not everyone will experience them.

Very common: may affect more than 1 in 10 people

• Dizziness (may lead to falls), headache, dry mouth.
• Sensation of drowsiness (which may disappear over time as you continue to take quetiapine), (may lead to falls).
• Withdrawal symptoms (symptoms that occur when you stop taking quetiapine), which include insomnia, nausea, headache, diarrhea, vomiting, dizziness, and irritability. A gradual withdrawal over a period of at least 1 to 2 weeks is recommended.
• Weight gain.
• Abnormal muscle movements. These include difficulty initiating muscle movements, tremor, feeling of restlessness or muscle rigidity without pain.
• Changes in the amount of certain fats (triglycerides and total cholesterol).

Common: may affect up to 1 in 10 people

• Fast heart rate.

• Feeling like your heart is beating strongly, beating quickly, or having irregular heartbeats.
• Constipation, indigestion.
• Sensation of weakness.
• Swelling of arms or legs.
• Low blood pressure when standing. This may make you feel dizzy or faint (may lead to falls).
• Increased levels of sugar in the blood.
• Blurred vision.
• Abnormal dreams and nightmares.
• Feeling hungrier.
• Feeling irritable.
• Speech and language disorder.
• Thoughts of suicide and worsening of depression.
• Shortness of breath.
• Vomiting (mainly in older people).
• Fever.
• Changes in the amount of thyroid hormones in the blood.
• Decrease in the number of certain types of blood cells.
• Increases in the amount of liver enzymes measured in the blood.
• Increases in the amount of prolactin hormone in the blood. Increases in prolactin hormone may, in rare cases, lead to:

orBoth men and women having breast swelling and unexpected milk production.

orWomen not having a menstrual period or having irregular periods.

Uncommon: may affect up to 1 in 100 people

• Seizures or convulsions.
• Allergic reactions that may include hives, skin swelling, and swelling around the mouth.
• Unpleasant sensations in the legs (also known as restless leg syndrome).
• Difficulty swallowing.
• Uncontrolled movements, mainly of the face or tongue.
• Sexual dysfunction.
• Diabetes.
• Change in the heart's electrical activity seen on an ECG (prolongation of the QT interval).
• Slower than normal heart rate that may occur at the start of treatment and may be associated with low blood pressure and fainting.
• Difficulty urinating.
• Fainting (may lead to falls).
• Stuffy nose.
• Decrease in the number of red blood cells in the blood.

• Decrease in the amount of sodium in the blood.
• Worsening of pre-existing diabetes.

Rare: may affect up to 1 in 1,000 people

• A combination of high temperature (fever), sweating, muscle stiffness, feeling very drowsy or dizzy (a condition known as "neuroleptic malignant syndrome").
• Yellowing of the skin and eyes (jaundice).
• Inflammation of the liver (hepatitis).
• Prolonged and painful erection (priapism).
• Breast swelling and unexpected milk production (galactorrhea).
• Menstrual disorder.

• Clots in the veins, especially in the legs (symptoms include swelling, pain, and redness in the leg), which may travel through the blood vessels to the lungs, causing chest pain and difficulty breathing. If you notice any of these symptoms, seek immediate medical attention.
• Walking, talking, eating, or other activities while asleep.
• Decrease in body temperature (hypothermia).
• Inflammation of the pancreas.
• A condition (called "metabolic syndrome") where you may experience a combination of 3 or more of the following effects: increased fat around your abdomen, decreased "good" cholesterol (HDL-C), increased levels of a type of fat in the blood called triglycerides, increased blood pressure, and increased blood sugar.
• A combination of fever, symptoms similar to the flu, sore throat, or any other infection with a very low white blood cell count, a condition known as agranulocytosis.
• Intestinal obstruction.
• Increased creatine phosphokinase in the blood (a substance found in muscles).

Very rare: may affect up to 1 in 10,000 people

• Severe rash, blisters, or red spots on the skin.
• Severe allergic reaction (known as anaphylaxis) that may cause difficulty breathing or shock.
• Quick swelling of the skin, usually around the eyes, lips, and throat (angioedema).
• Severe skin blistering, mouth, eyes, and genital areas (Stevens-Johnson syndrome).
• Abnormal secretion of a hormone that controls urine volume.
• Rhabdomyolysis, a condition where muscle fibers break down and cause muscle pain.

Unknown: the frequency cannot be estimated from available data

• Skin rash with irregular red spots (erythema multiforme).
• Sudden and severe allergic reaction with symptoms such as fever and blisters on the skin and peeling of the skin (toxic epidermal necrolysis).
• Withdrawal symptoms may occur in newborn babies of mothers who have taken quetiapine during pregnancy.
• Stroke.
• Cardiomyopathy, a disorder of the heart muscle.
• Myocarditis, inflammation of the heart muscle.
• Vasculitis, inflammation of the blood vessels, often with a skin rash of small red or purple spots.

The class of medicines to which quetiapine belongs can cause heart rhythm problems that may be serious and, in severe cases, fatal.

Some side effects are only seen when a blood test is done. These include changes in the amount of certain fats (triglycerides and total cholesterol) or sugar in the blood, changes in the amount of thyroid hormones in the blood, increases in liver enzymes, decreases in the number of certain types of blood cells, decreases in the number of red blood cells, increases in creatine phosphokinase in the blood (a substance found in muscles), decreases in the amount of sodium in the blood, and increases in the amount of prolactin hormone in the blood. Increases in prolactin hormone may, in rare cases, lead to:

• Both men and women having breast swelling and unexpected milk production.
• Women not having a menstrual period or having irregular periods.

Your doctor may ask you to have blood tests from time to time.

Additional side effects in children and adolescents

The same side effects that may occur in adults may also occur in children and adolescents.

The following side effects have been observed more frequently in children and adolescents or have not been observed in adults:

Very common: may affect more than 1 in 10 people

• Increased amount of a hormone called prolactin in the blood. Increases in prolactin hormone may, in rare cases, lead to:

orBoth boys and girls having breast swelling and unexpected milk production.

orGirls not having a menstrual period or having irregular periods.

• Increased appetite.
• Vomiting.
• Abnormal muscle movements. These include difficulty initiating muscle movements, tremors, feeling of restlessness or muscle rigidity without pain.
• Increased blood pressure.

Common: may affect up to 1 in 10 people

• Sensation of weakness, fainting (may lead to falls).
• Stuffy nose.
• Feeling irritable.

Reporting of side effects

If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for the Vigilance of Medicines for Human Use: www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.

Keepthis medicationout of the reach and sight of children.

Do not usethis medicationafter the expiration date that appears on thepackagingafter CAD. The expiration date is the last day of the month indicated.

This medication does not require special storage conditions.

Medications should not be disposed of through drains or trash.Deposit the packaging and medications you no longer need at the SIGRE collection pointat the pharmacy. If in doubt, please ask your pharmacisthow to dispose ofthepackaging and themedications you no longerneed.By doing so, you will help protect the environment.

Composition of Quetiapina pensa

- The active ingredient is quetiapine. Quetiapina pensa tablets contain 150 mg of quetiapine (as quetiapine fumarate).

- The other components are:

Tablet core:Acrylate and methacrylic acid copolymer (1:1), type A, anhydrous lactose, crystalline maltose, talc, magnesium stearate

Tablet coating: Acrylate and methacrylic acid copolymer (1:1), triethyl citrate.

Appearance of Quetiapina pensa and content of the container

Quetiapina pensa 150 mg tablets are white or off-white, oblong, biconvex, and marked with “150” on one face.

Tablets are packaged in PVC/PCTFE-Aluminum blisters containing 60 tablets.

Holder of the marketing authorization and responsible for manufacturing

Holder of the marketing authorization

Towa Pharmaceutical, S.A.

C/ de Sant Martí, 75-97

08107 Martorelles (Barcelona)

Spain

Responsible for manufacturing

Pharmathen International S.A

Industrial Park Sapes,

Rodopi Prefecture, Block No 5,

Rodopi 69300,

Greece

or

Pharmathen S.A.

Dervenakion 6

Pallini 15351

Attiki,

Greece

Last review date of thisleaflet:May 2024

The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es