


Ask a doctor about a prescription for QUETIAPINE CINFA 400 mg PROLONGED-RELEASE TABLETS
Package Leaflet: Information for the Patient
quetiapine cinfa 400 mg prolonged-release tablets EFG
Quetiapine
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack:
quetiapine cinfa contains a substance called quetiapine. It belongs to a group of medicines called antipsychotics. quetiapine cinfa can be used to treat several diseases, such as:
When quetiapine cinfa is used 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 to prescribe quetiapine cinfa even when you are feeling better.
Do not take quetiapine cinfa
If you are in doubt, consult your doctor or pharmacist before taking quetiapine.
Warnings and precautions
Consult your doctor or pharmacist before starting to take quetiapine cinfa:
Tell your doctor immediately if you experience any of the following after taking quetiapine cinfa:
These disorders can be caused by this type of medication.
Tell your doctor as soon as possible if you experience:
Suicidal thoughts and worsening of your depression
If you are depressed, you may sometimes think about harming yourself or committing suicide. This can increase when you first start treatment, as all these medications take time to work, usually around two weeks, but sometimes more. These thoughts can 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 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 be helpful to tell a family member or close friend that you are depressed and ask them to read this leaflet. You can ask them to tell you if they think your depression is getting worse, or if they are concerned about changes in your behavior.
Severe skin reactions (SCARs)
With the use of this medication, very rare severe skin reactions (SCARs) have been reported, which can be life-threatening or fatal. These are commonly manifested as:
If you develop these symptoms, stop using quetiapine and contact your doctor or seek medical attention immediately.
Weight gain
Weight gain has been observed in patients taking quetiapine. You and your doctor should monitor your weight regularly.
Children and adolescents
quetiapine cinfa is not indicated for use in children or adolescents under 18 years of age.
Other medications and quetiapine cinfa
Tell your doctor if you are taking, have recently taken, or might take any other medications.
Do not take quetiapine cinfa if you are using any of the following medications:
Tell your doctor if you are using any of the following medications:
Before stopping any of your medications, consult your doctor first.
quetiapine cinfa with food, drinks, and alcohol
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor before using this medication. You should not take quetiapine cinfa during pregnancy, unless your doctor has advised you to do so. You should not use quetiapine cinfa if you are breastfeeding.
The following symptoms, which may represent withdrawal symptoms, may occur in the newborn baby, whose mothers have taken quetiapine in the third trimester of pregnancy (last three months of pregnancy): tremors, muscle stiffness and/or weakness, drowsiness, agitation, breathing problems, and difficulty feeding. If your baby develops any of these symptoms, you may need to contact your doctor.
Driving and using machines
quetiapine cinfa can cause symptoms such as drowsiness, dizziness, or changes in vision, and can reduce your reaction ability. These effects, as well as the disease itself, can make it difficult for you to drive vehicles or operate machines. Therefore, do not drive, operate machines, or engage in other activities that require special attention until your doctor assesses your response to this medication.
Effect on drug detection tests in urine
If you are undergoing a urine drug detection test, quetiapine cinfa may produce positive results for methadone or certain antidepressant medications called tricyclic antidepressants (TCAs) when some analysis methods are used, even if you are not taking methadone or TCAs. If this occurs, a more specific test can be performed.
quetiapine cinfa contains sodium
This medication contains less than 1 mmol of sodium (23 mg) per tablet; that is, it is essentially "sodium-free".
Follow the administration instructions of this medication exactly as indicated by your doctor. 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 disease and needs, but it will usually be between 150 mg and 800 mg.
Liver problems
If you have liver problems, your doctor may change your dose.
Elderly patients
If you are an elderly patient, your doctor may change your dose.
Use in children and adolescents
quetiapine cinfa should not be used by children and adolescents under 18 years of age.
If you take more quetiapine cinfa than you should
If you take more quetiapine cinfa than your doctor has prescribed, you may feel drowsy, dizzy, and experience abnormal heartbeats. In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, Telephone 915 620 420, indicating the medication and the amount ingested. Bring the quetiapine cinfa tablets with you.
If you forget to take quetiapine cinfa
If you forget to take a dose, take it as soon as you remember. If it is close to the time for your next dose, wait until then. Do not take a double dose to make up for forgotten doses.
If you stop taking quetiapine cinfa
If you stop taking quetiapine cinfa abruptly, you may be unable to sleep (insomnia), or you may feel nauseous, 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 adverse effects, although not all people suffer from them.
If you experience any of the following serious adverse effects, stop taking quetiapine cinfaand go to your doctor or the nearest hospital:
Adverse EffectsFrequently(may affect up to 1 in 10 people)
Adverse Effects Less Frequently(may affect up to 1 in 100 people)
Adverse Effects Rarely(may affect up to 1 in 1,000 people)
Adverse Effects Very Rarely(may affect up to 1 in 10,000 people)
Unknown(frequency cannot be estimated from available data)
Drug rash with eosinophilia and systemic symptoms (DRESS, for its acronym in English): Generalized rash, elevated body temperature, elevated liver enzymes, blood abnormalities (eosinophilia), enlarged lymph nodes, and other organs involved (drug rash with eosinophilia and systemic symptoms, also known as DRESS). If you develop these symptoms, stop using quetiapine and contact your doctor or seek immediate medical attention.
Do not worry if you see a tablet in your stoolafter taking quetiapine cinfa. As the tablet passes through the gastrointestinal tract, quetiapine is slowly released. The tablet form remains undissolved and is eliminated in the stool. Therefore, even if you see a tablet in your stool, your dose of quetiapine has been absorbed.
Other Possible Adverse Effects:
Adverse Effects Very Frequently(may affect more than 1 in 10 people)
Adverse EffectsFrequently(may affect up to 1 in 10 people)
Adverse Effects Less Frequently(may affect up to 1 in 100 people)
Adverse Effects Rarely(may affect up to 1 in 1,000 people)
Adverse Effects Very Rarely(may affect up to 1 in 10,000 people)
Unknown(frequency cannot be estimated from available data)
Some adverse effects are only observed when a blood test is performed. 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, increased liver enzymes, decreased number of certain types of blood cells, decreased number of red blood cells, increased creatine phosphokinase in the blood (a substance from muscles), decreased sodium in the blood, and an increase in the amount of prolactin hormone in the blood.
The increases in prolactin hormone could, in rare cases, lead to the following:
Your doctor may ask you to have blood tests from time to time.
Adverse Effects in Children and Adolescents
The same adverse effects that can occur in adults can also occur in children and adolescents.
The following adverse effects have been observed more frequently in children and adolescents or have not been observed in adults:
Adverse Effects Very Frequently(may affect more than 1 in 10 people)
Adverse EffectsFrequently(may affect up to 1 in 10 people)
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that does not appear in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of sight and reach of children.
Do not use this medicine after the expiration date that appears on the packaging and on the blister after CAD. The expiration date is the last day of the month indicated.
Store in the original packaging to protect it from moisture.
This medicine does not require any special storage temperature.
After the first opening of the HDPE bottle, the product must be used within 60 days.
Medicines should not be thrown away through wastewater or household waste. Deposit the packaging and medicines you no longer need in the SIGRE Point of the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medicines you no longer need. This way, you will help protect the environment.
Composition of Qutiapine Cinfa
Core: hypromellose, microcrystalline cellulose, anhydrous sodium citrate, magnesium stearate. Coating: titanium dioxide (E171), hypromellose, macrogol/PEG 400, and polysorbate 80.
Appearance of the Product and Package Contents
Qutiapine Cinfa 400 mg prolonged-release tablets EFG
They are coated tablets, white, biconvex, oblong, and engraved with "Q 400" on one side.
Packaging of 10, 20, 30, 50, 50x1 (perforated unit-dose blister) (hospital packaging), 56 (calendar packaging), 60, 90, and 100 tablets.
HDPE bottles containing 60 tablets.
Not all packaging sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Laboratorios Cinfa, S.A.
Carretera Olaz-Chipi, 10. Polígono Industrial Areta.
31620 Huarte (Navarra) - Spain
Manufacturer
TEVA Pharmaceutical Works Private Limited Company
Pallagi út 13, H-4042 Debrecen
Hungary
Pharmachemie B.V.
Swensweg 5, P.O. Box 552 NL 2003 RN Haarlem
Netherlands
Teva Czech Industries s.r.o.
Ostravska 29, c.p. 305, Building No 80 Small OSD and Building No 881 NOSD
74770 Opava-Komarov
Czech Republic
TEVA OPERATIONS POLAND SP.Z.O.O.
ul. Mogilska 80, 31-546, Krakow
Poland
Teva Pharma, S.L.U.
C/C, n. 4, Polígono Industrial Malpica, 50016 Zaragoza
Spain
Merckle GmbH
Ludwig-Merckle-Straße 3, 89143 Blaubeuren
Germany
Date of the Last Revision of thisLeaflet:June 2024
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
You can access detailed and updated information about this medicine by scanning the QR code included in the leaflet and packaging with your mobile phone (smartphone). You can also access this information at the following internet address: https://cima.aemps.es/cima/dochtml/p/75503/P_75503.html
QR code to: https://cima.aemps.es/cima/dochtml/p/75503/P_75503.html
The average price of QUETIAPINE CINFA 400 mg PROLONGED-RELEASE TABLETS in November, 2025 is around 129.63 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for QUETIAPINE CINFA 400 mg PROLONGED-RELEASE TABLETS – subject to medical assessment and local rules.