Quetiapine Farmaprojects 300 mg film-coated tablets EFG
Spain
Table of Contents
- Package leaflet: Information for the user
- Introduction
- 1. What Quetiapine Farmaprojects is and what it is used for
- 2. What you need to know before taking Quetiapina Farmaprojects
- 3. How to take Quetiapine Farmaprojects
- 4. Possible adverse effects
- 5. Storage of Quetiapine Farmaprojects
- 6. Contents of the pack and other information
Package leaflet: Information for the user
Introduction
Package leaflet: information for the user
Read the entire leaflet carefully before you start taking this medicine, because it contains important information for you.
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Keep this leaflet, as you may need to read it again. If you have any questions, ask your doctor or pharmacist.
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This medicine has been prescribed for you only, and you should not give it to others, even if they have the same symptoms as you, because it could harm them.
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If you experience any adverse effects, consult your doctor or pharmacist, even if they are effects not listed in this leaflet. See section 4.
Contents of the leaflet
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What Quetiapine Farmaprojects is and what it is used for
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What you need to know before taking Quetiapine Farmaprojects
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How to take Quetiapine Farmaprojects
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Possible side effects
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Storage of Quetiapine Farmaprojects
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Contents of the pack and other information
1. What Quetiapine Farmaprojects is and what it is used for
This medicine contains a substance called quetiapine. It belongs to a group of medicines known as antipsychotics. Quetiapine may be used to treat several conditions, such as:
- Bipolar depression: when you feel sad. You may find that you feel depressed, guilty, lack energy, lose your appetite, or are unable to sleep.
- Mania: when you may feel extremely excited, euphoric, agitated, enthusiastic, or hyperactive, or have poor judgment, which may include being aggressive or violent.
- Schizophrenia: when 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.
Your doctor may continue to prescribe this medicine even after you start feeling better.
2. What you need to know before taking Quetiapina Farmaprojects
Do not take quetiapine:
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if you are allergic to quetiapine or any of the other ingredients of this medicine (listed in section 6).
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if you are taking any of the following medicines:
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Certain medicines for HIV
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Azole-type medicines (for fungal infections)
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Erythromycin or clarithromycin (for infections)
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Nefazodone (for depression).
If you have any doubts, consult your doctor or pharmacist before taking quetiapine.
Warnings and precautions
Talk to your doctor or pharmacist before starting Quetiapina Farmaprojects:
- If you suffer from depression or other conditions treated with antidepressants. The use of these medicines together with Quetiapina Farmaprojects may cause serotonin syndrome, a potentially life-threatening condition (see "Other medicines and Quetiapina Farmaprojects").
- if you, or a family member, have or have had any heart problems, for example, irregular heartbeat, weakened 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. If so, your doctor may monitor your blood sugar levels while you are taking quetiapine.
- if you know you have previously had low levels of white blood cells (which may or may not have been caused by other medicines).
- if you are an elderly person with dementia (loss of brain function). In this case, you should not take quetiapine, as the group of medicines to which quetiapine belongs may increase the risk of stroke or, in some cases, death in these individuals.
- 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 this have been associated with blood clot formation.
- if you have or have had a condition in which your breathing stops briefly during normal sleep (called "sleep apnea") and you are taking medicines that reduce normal brain activity ("depressants").
- if you have or have had a condition in which you cannot completely empty your bladder (urinary retention), an enlarged prostate, intestinal obstruction, or increased pressure inside your eye. These conditions may sometimes be caused by medicines (called "anticholinergics") that affect how nerve cells function, used to treat certain medical conditions.
- if you have a history of alcohol or drug abuse.
Inform your doctor immediately if, after taking quetiapine, you experience any of the following:
- A combination of fever, severe muscle stiffness, sweating, or decreased level of consciousness (a disorder known as "neuroleptic malignant syndrome"). Immediate medical treatment may be required.
- Uncontrollable movements, mainly of your face or tongue.
- Dizziness or feeling very sleepy. This may increase the risk of accidental injuries (falls) in elderly patients.
- Seizures (convulsions).
- A prolonged and painful erection (priapism).
- Fast or irregular heartbeat, even at rest, palpitations, breathing difficulties, chest pain, or unexplained tiredness. Your doctor should examine your heart and, if necessary, refer you immediately to a cardiologist.
These disorders 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 this could be due to a very low count of white blood cells and may require stopping treatment with quetiapine and/or additional treatment.
- Constipation along with persistent abdominal pain, or constipation that has not responded to treatment, as this could lead to a more serious intestinal blockage.
- Suicidal thoughts and worsening of your 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 work—usually about two weeks, but sometimes longer. These thoughts may also increase if you stop your medication abruptly. You may be more likely to have such thoughts if you are a young adult. Data from clinical trials have shown an increased risk of suicidal thoughts and/or suicidal behavior in young adults under 25 years of age with depression.
If at any time you 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 inform you if they think your depression is worsening or if they are concerned about changes in your behavior.
Serious skin adverse reactions (SCARs)
Very rarely, serious skin adverse reactions (SCARs) have been reported with this medicine, which may be life-threatening or fatal. These commonly manifest as:
- Stevens-Johnson syndrome (SJS), a widespread rash with blisters and skin peeling, particularly around the mouth, nose, eyes, and genitals.
- Toxic epidermal necrolysis (TEN), a more severe form causing extensive skin peeling.
- Drug reaction with eosinophilia and systemic symptoms (DRESS), characterized by flu-like symptoms with rash, fever, swollen lymph nodes, and abnormal blood test results (including increased white blood cells (eosinophilia) and elevated liver enzymes).
- Acute generalized exanthematous pustulosis (AGEP), small pustules filled with pus.
- Erythema multiforme (EM), skin rashes with irregular red spots that itch.
If you develop any of these symptoms, stop using quetiapine and contact your doctor or seek immediate medical attention.
Weight gain
Weight gain has been observed in patients taking quetiapine. You and your doctor should monitor your weight regularly.
Children and adolescents
Quetiapine must not be used in children and adolescents under 18 years of age.
Other medicines and Quetiapina Farmaprojects
Tell your doctor if you are taking, have recently taken, or might need to take any other medicine.
Do not take quetiapine if you are using any of the following medicines:
- Certain medicines for HIV.
- Azole-type medicines (for fungal infections).
- Erythromycin or clarithromycin (for infections).
- Nefazodone (for depression).
Inform your doctor if you are taking any of the following medicines:
- Medicines for epilepsy (such as phenytoin or carbamazepine).
- Medicines for high blood pressure.
- Barbiturates (for difficulty sleeping).
- Thioridazine or lithium (other antipsychotic medicines).
- Medicines that may affect your heart rhythm, for example, medicines that can cause an electrolyte imbalance (low levels of potassium or magnesium), such as diuretics (medicines to increase urination) or certain antibiotics (medicines to treat infections).
- Medicines that may cause constipation.
- Medicines (called "anticholinergics") that affect how nerve cells function, used to treat certain medical conditions.
- Antidepressants. These medicines may interact with Quetiapina Farmaprojects, and you may experience symptoms such as involuntary and rhythmic muscle contractions, including muscles controlling eye movement, agitation, hallucinations, coma, excessive sweating, tremor, exaggerated reflexes, increased muscle tension, and body temperature above 38°C (serotonin syndrome). Contact your doctor if you experience these symptoms.
Before stopping any of your medicines, consult your doctor first.
Taking quetiapine with food, drinks, and alcohol
- Quetiapine may be taken with or without food.
- Be cautious about the amount of alcohol you consume. This is because the combined effect of quetiapine and alcohol may make you drowsy.
- Do not drink grapefruit juice while taking quetiapine. It may affect how the medicine works.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
You must not take quetiapine during pregnancy unless advised by your doctor. You must not use quetiapine if you are breastfeeding.
The following symptoms, which may represent withdrawal syndrome, may occur in newborns of mothers who have used quetiapine during the third trimester (last three months of pregnancy): tremor, muscle stiffness and/or weakness, drowsiness, agitation, breathing difficulties, and feeding problems. If your newborn develops any of these symptoms, you may need to contact your doctor.
Driving and using machines
Quetiapine may cause symptoms such as drowsiness, dizziness, or vision disturbances, and may reduce reaction ability. These effects, as well as the illness itself, may impair your ability to drive or operate machinery. Therefore, do not drive or operate machinery, or engage in other activities requiring special attention, until your doctor has assessed your response to this medicine.
Quetiapine contains lactose
This medicine contains lactose, a type of sugar. If your doctor has informed you that you have an intolerance to certain sugars, consult with him before taking this medicine.
Quetiapine contains sodium:
This medicine contains less than 23 mg of sodium (1 mmol) per tablet, which is essentially "sodium-free".
Effect on Urine Drug Screening Tests
If you are undergoing a urine drug screening test, taking quetiapine may produce positive results for methadone or certain antidepressant medicines known as tricyclic antidepressants (TCAs) when certain testing methods are used, even if you are not taking methadone or TCAs. If this occurs, a more specific test can be performed.
3. How to take Quetiapine Farmaprojects
Follow exactly the instructions for using this medicine given by your doctor. If in doubt, consult your doctor or pharmacist again.
Your doctor will decide your starting dose. The maintenance dose (daily dose) will depend on your condition and individual needs, but will usually be between 150 mg and 800 mg.
- You will take your tablets once daily at bedtime or twice daily, depending on your condition.
- Swallow your tablets whole with water.
- You may take the tablets with or without food.
- Do not drink grapefruit juice while taking quetiapine. It may affect how the medicine 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 adjust your dose.
Elderly patients
If you are elderly, your doctor may adjust your dose.
Use in children and adolescents
Quetiapine must not be used in children and adolescents under 18 years of age.
If you take more quetiapine than you should
If you take more quetiapine than prescribed by your doctor, you may feel drowsy, dizzy, or experience abnormal heartbeats. Contact your doctor or nearest hospital immediately. Take the quetiapine tablets with you.
You may also contact your pharmacist or call the Toxicology Information Service at 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to take quetiapine
If you forget to take a dose, take it as soon as you remember. If it is almost time for your next dose, wait until then. Do not take a double dose to make up for a missed dose.
If you stop taking quetiapine
If you stop taking quetiapine abruptly, you may have difficulty sleeping (insomnia), feel nauseous, or experience headache, diarrhea, vomiting, dizziness, or irritability. Your doctor may advise you to gradually reduce the dose before stopping treatment.
If you have any further questions about the use of this medicine, ask your doctor or pharmacist.
4. Possible adverse effects
Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.
Very common: may affect more than 1 in 10 people
- Dizziness (could lead to falls), headache, dry mouth.
- Drowsiness (which may disappear over time as you continue taking quetiapine) (could lead to falls).
- Withdrawal symptoms (symptoms that occur when you stop taking quetiapine), including inability to sleep (insomnia), feeling nauseous, headache, diarrhoea, vomiting, dizziness, and irritability. 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, restlessness, or painless muscle stiffness.
- Changes in levels of certain fats (triglycerides and total cholesterol).
Common: may affect up to 1 in 10 people
- Fast heartbeat.
- Feeling as if your heart is beating strongly, racing, or skipping beats.
- Constipation, upset stomach (indigestion).
- Feeling weak.
- Swelling of arms or legs.
- Low blood pressure when standing. This may make you feel dizzy or faint (could lead to falls).
- Increased blood sugar levels.
- Blurred vision.
- Abnormal dreams and nightmares.
- Increased appetite.
- Feeling irritable.
- Speech and language disorders.
- Suicidal thoughts and worsening of depression.
- Shortness of breath.
- Vomiting (mainly in elderly people).
- Fever.
- Changes in levels of thyroid hormones in the blood.
- Decreased number of certain types of blood cells.
- Increases in liver enzyme levels measured in blood.
- Increases in prolactin hormone levels in blood. Elevated prolactin levels may, in rare cases, lead to:
- Breast enlargement and unexpected milk production in both men and women.
- In women, absence of menstrual periods or irregular periods.
Uncommon: may affect up to 1 in 100 people
- Epileptic seizures or convulsions.
- Allergic reactions which may include raised, itchy rashes (hives), skin swelling, or swelling around the mouth.
- Unpleasant sensations in the legs (also known as restless legs syndrome).
- Difficulty swallowing.
- Uncontrolled movements, mainly of the face or tongue.
- Sexual dysfunction.
- Diabetes.
- Changes in the electrical activity of the heart seen on ECG (prolongation of the QT interval).
- Slower than normal heart rate, which may occur at the beginning of treatment and may be associated with low blood pressure and fainting.
- Difficulty urinating.
- Fainting (could lead to falls).
- Stuffy nose.
- Decrease in the number of red blood cells in the blood.
- Decrease in sodium levels in the blood.
- Worsening of pre-existing diabetes.
- Confusion.
Rare: may affect up to 1 in 1,000 people
- A combination of high temperature (fever), sweating, muscle stiffness, and extreme drowsiness or dizziness (a condition called "neuroleptic malignant syndrome").
- Yellowing of the skin and eyes (jaundice).
- Inflammation of the liver (hepatitis).
- Prolonged and painful erection (priapism).
- Breast enlargement and unexpected milk production (galactorrhoea).
- Menstrual disorders.
- Blood clots in veins, 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 breathing. If you notice any of these symptoms, seek immediate medical attention.
- Walking, talking, eating, or other activities while asleep.
- Decreased body temperature (hypothermia).
- Inflammation of the pancreas.
- A condition (called “metabolic syndrome”) in which you may have 3 or more of the following effects: increased abdominal fat, 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, flu-like symptoms, sore throat, or any other infection with a very low white blood cell count, a condition known as agranulocytosis.
- Intestinal obstruction.
- Increased blood creatine phosphokinase (a substance from muscles).
Very rare: may affect up to 1 in 10,000 people
- Severe rash, blisters, or red spots on the skin.
- Severe allergic reaction (called anaphylaxis) which may cause difficulty breathing or shock.
- Rapid swelling of the skin, usually around the eyes, lips, and throat (angioedema).
- A serious condition with blisters on the skin, mouth, eyes, and genitals (Stevens-Johnson syndrome). See section 2.
- Inappropriate secretion of a hormone that controls urine volume.
- Breakdown of muscle fibres and muscle pain (rhabdomyolysis).
Not known: frequency cannot be estimated from available data
- Skin rashes with irregular red spots (erythema multiforme). See section 2.
- Rapid appearance of red skin areas with small pustules (small blisters filled with white/yellow fluid known as Acute Generalized Exanthematous Pustulosis (AGEP). See section 2.
- Sudden and severe allergic reaction with symptoms such as fever, skin blisters, and skin peeling (toxic epidermal necrolysis). See section 2.
- Drug reaction with eosinophilia and systemic symptoms (DRESS), which includes flu-like symptoms with rash, fever, swollen lymph nodes, and abnormal blood test results (including increased white blood cells (eosinophilia) and elevated liver enzymes). See section 2.
- Withdrawal symptoms may occur in newborns of mothers who have used quetiapine during pregnancy.
- Stroke.
- Heart muscle disorder (cardiomyopathy).
- Inflammation of the heart muscle (myocarditis).
- Inflammation of blood vessels (vasculitis), often with a skin rash showing small red or purple spots.
The class of medicines to which quetiapine belongs can cause problems with heart rhythm that may be serious and, in severe cases, could be fatal.
Some adverse effects are only detected by blood tests. These include changes in levels of certain fats (triglycerides and total cholesterol) or blood sugar, changes in thyroid hormone levels in the blood, increases in liver enzymes, decreases in the number of certain types of blood cells, decrease in red blood cells, increased blood creatine phosphokinase (a substance found in muscles), decreased sodium levels in blood, and increased levels of prolactin hormone in blood. Elevated prolactin levels may, in rare cases, lead to:
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Breast enlargement and unexpected milk production in both men and women.
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In women, absence of menstrual periods or irregular periods.
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Your doctor may ask you to have blood tests from time to time.
Other adverse effects in children and adolescents
The same adverse effects that may occur in adults may also occur in children and adolescents.
The following adverse effects have been observed more frequently in children and adolescents, or were not observed in adults:
Very common: may affect more than 1 in 10 people
- Increased levels of a hormone called prolactin in the blood. Elevated prolactin levels may, in rare cases, lead to:
- Breast enlargement and unexpected milk production in both boys and girls.
- In girls, absence of menstrual periods or irregular periods.
- Increased appetite.
- Vomiting.
- Abnormal muscle movements. These include difficulty initiating muscle movements, tremors, restlessness, or painless muscle stiffness.
- Increased blood pressure.
Common: may affect up to 1 in 10 people
- Feeling weak, fainting (could lead to falls).
- Stuffy nose.
- Feeling irritable.
Reporting of adverse effects
If you experience any adverse effect, talk to your doctor or pharmacist, even if it is a possible adverse effect not listed in this leaflet. You can also report them directly via the Spanish Pharmacovigilance System for Human Medicines: www.notificaRAM.es. By reporting adverse effects, you can help provide more information on the safety of this medicine.
5. Storage of Quetiapine Farmaprojects
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the carton and blister after EXP. The expiry date refers to the last day of the month indicated.
This medicine does not require any special storage conditions.
Medicines must not be disposed of via wastewater or household waste. Return unused medicines and their containers to your pharmacy’s SIGRE collection point. If you are unsure, ask your pharmacist how to dispose of medicines and containers you no longer need. This will help protect the environment.
6. Contents of the pack and other information
Composition of Quetiapina Farmaprojects
- The active substance is quetiapine. Quetiapina Farmaprojects tablets contain 100 mg of quetiapine (as quetiapine fumarate).
- The other components are:
Tablet core: povidone K30, microcrystalline cellulose, calcium hydrogen phosphate dihydrate, potato starch carboxymethyl ether type C, colloidal anhydrous silica, magnesium stearate.
Tablet coating: hypromellose, lactose monohydrate, macrogol 3350, triacetin, and titanium dioxide (E-171).
Appearance of the product and contents of the pack
Quetiapine 300 mg film-coated tablets are white, oblong, and have a score line on one side.
They are packed in containers of 60 tablets.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Farmaprojects S.A.U
C/Provença 392
6th Floor
08025 Barcelona
Spain
Manufacturer
Zaklady Farmaceutyczne Polpharma SA
(Pharmaceutical Works Polpharma SA)
ul. Pelplinska 19
83-200 Starogard Gdanski
Poland
Date of the most recent review of this leaflet: August 2025
Other sources of information
Detailed information about this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/)