Leaflet: information for theuser
Besitran 50mg film-coated tablets
Sertralina
Read this leaflet carefully before you start taking thismedicine, because it contains important information for you.
1. What isBesitranand what it is used for
2. What you need to know before taking Besitran
3. How to take Besitran
4. Possible side effects
5. Storage of Besitran
6. Contents of the pack and additional information
Besitrancontains sertraline as the active ingredient. Sertralinebelongs to a group of medications known asInhibitors ofSelective Serotonin Reuptake(ISRS); these medications are used to treat depression and/or anxiety disorders.
Besitrancan be used to treat:
Depression is a clinical disease with symptoms such as feelings of sadness, inability to sleep well or to enjoy life as one used to.
OCD and anxiety disorders are anxiety-related diseases with symptoms such as being constantly preoccupied with repeated ideas (obsessions) that lead to repetitive rituals (compulsions).
PTSD is a disorder that may occur after a very emotionally traumatic experience, and has some symptoms similar to depression and anxiety. Social anxiety disorder (social phobia) is an anxiety-related disease. It is characterized by intense anxiety or anguish in social situations (for example: speaking to strangers, speaking in public, eating or drinking in front of others, or worrying about behaving in a shameful manner).
Your doctor has considered this medication suitable for treating your condition.
If you are unsure why you have been prescribed Besitran, you should consult your doctor.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Besitran.
Medicines are not always suitable for everyone. Before starting treatment with Besitran, tell your doctor if you have or have had any of the following circumstances:
Restlessness/Acatisia:
The use of sertraline has been associated with unpleasant restlessness and a need to move, often accompanied by an inability to sit or stand still (acatisia). This occurs more often during the first few weeks of treatment. Increasing the dose may be harmful, so if you develop these symptoms, you should contact your doctor.
Withdrawal symptoms:
Side effects related to stopping treatment (withdrawal symptoms) are common, particularly if treatment is stopped abruptly (see section 3. If you stop taking Besitran and section 4. Possible side effects). The risk of withdrawal symptoms depends on the duration of treatment, the dose, and the rate at which the dose is reduced. Generally, these symptoms are mild or moderate. However, in some patients, they can be severe. These symptoms usually occur during the first few days after stopping treatment. In general, these symptoms usually resolve on their own and usually resolve within two weeks. In some patients, they may last longer (2-3 months or more). It is recommended that when stopping treatment with sertraline, the dose be gradually reduced over a period of several weeks or even months, and you should always agree with your doctor on the best way to stop treatment.
Thoughts of suicide and worsening of your depression or anxiety:
If you are depressed and/or have anxiety disorders, you may have thoughts of harming yourself or committing suicide. This may increase at the beginning of treatment with antidepressants, as all these medications take time to take effect, which is usually two weeks but sometimes longer.
You are more likely to experience this:
If you have thoughts of harming yourself or committing suicide at any time, contact your doctor or go to the hospital immediately.
It may be helpful for you to explain to a close family member or friend that you are depressed or have anxiety, and ask them to read this leaflet. You can also ask them to tell you if they think your depression or anxiety is getting worse, or if they are concerned about changes in your behavior.
Some medications in the group to which Besitran belongs (called ISRS) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms persist after stopping treatment.
Children and adolescents:
Normally, sertraline should not be used to treat children and adolescents under 18 years old, except in the case of patients with obsessive-compulsive disorder (OCD). Young patients are at greater risk of side effects such as attempts to commit suicide, thoughts of harming themselves or committing suicide (suicidal thoughts), and hostility (predominantly aggression, confrontational behavior, and irritable reaction) when treated with this class of medications. However, your doctor may decide to prescribe Besitran to a patient under 18 years old if they consider it to be the most suitable option for the patient. If your doctor has prescribed Besitran and you are under 18 years old and want to discuss this decision, please return to your doctor. You should inform your doctor if any of the symptoms listed above appear or worsen when you are taking Besitran. The long-term effects on safety and related to growth, maturity, and learning (cognitive development) and behavioral development of Besitran were evaluated in a long-term study in over 900 children aged 6 to 16 years who were monitored for a period of 3 years. In general, the results of the study showed that children treated with sertraline developed normally, except for a slight increase in weight in those treated with a higher dose.
Other medications and Besitran:
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Some medications may affect how Besitran works, or Besitran itself may reduce the effectiveness of other medications you are taking at the same time.
The use of Besitran with the following medications may cause severe side effects:
Inform your doctor if you are taking the following medications:
Taking Besitran with food, drinks, and alcohol:
Besitran tablets can be taken with or without food.
Alcohol should be avoided while being treated with Besitran.
Do not take sertraline with grapefruit juice, as it may increase the levels of sertraline in your body.
Pregnancy, breastfeeding, and fertility:
If you are pregnant or breastfeeding, or think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
The safety of sertraline has not been fully established in pregnant women. If you are pregnant, sertraline will only be administered if your doctor considers that the benefits for you outweigh any possible risk to the developing fetus.
If you take Besitran in the final stages of pregnancy, there may be an increased risk of excessive vaginal bleeding shortly after delivery, especially if you have a history of bleeding disorders. Your doctor or midwife should know that you are taking Besitran so that they can advise you.Besitran may increase the risk of a serious condition in newborns called persistent pulmonary hypertension (PPHN), which causes the baby to breathe faster and appear blue. These symptoms usually start within the first 24 hours after birth. If this happens to your baby, contact your midwife and/or doctor immediately.
Your newborn baby may have other conditions, which usually manifest within the first 24 hours after birth. The symptoms include:
• difficulty breathing,
• blue skin or too hot or cold,
• blue lips,
• vomiting or feeding problems,
• excessive tiredness, unable to sleep, or crying a lot,
• muscle stiffness or decreased muscle tone,
• tremors, restlessness, or convulsions,
• increased reflexes,
• irritability,
• low blood sugar.
If your baby has any of these symptoms at birth, or you are concerned about your baby's health, consult your doctor or midwife for advice.
There is evidence that sertraline passes into breast milk. Therefore, sertraline can only be used in women while breastfeeding if your doctor considers that the benefits outweigh any possible risk to the baby.
In animal studies, some medications like sertraline have been shown to reduce sperm quality. Theoretically, this could affect fertility, but it has not been determined in humans.
Driving and operating machinery:
Psychotropic medications like sertraline can affect your ability to drive or operate machinery. Therefore, do not drive or operate heavy machinery until you know how this medication affects your ability to perform these activities.
This medication contains less than 23 mg of sodium (1 mmol) per tablet; this is, essentially "sodium-free".
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.
The recommended dose is:
Depression and Obsessive-Compulsive Disorder:
The usually effective dose for depression and OCD is 50mg per day. The daily dose can be increased by 50mg at intervals of at least one week, and thus forseveral weeks. The maximum recommended dose is 200mg per day.
Anxiety Disorder, Social Anxiety Disorder and Post-Traumatic Stress Disorder::
For anxiety disorder, social anxiety disorder and post-traumatic stress disorder, treatment should begin with a dose of 25mg per day, and increased to 50mg per day after one week.
The daily dose can be increased in intervals of 50mg over a period of several weeks. The maximum recommended dose is 200mg per day.
Use in children and adolescents:
Besitran should only be used to treat children and adolescents aged 6 to 17 years with OCD.
Obsessive-Compulsive Disorder:
Children aged 6 to 12 years:The recommended starting dose is 25mg per day. After one week, your doctor may increase the dose to 50mg per day. The maximum dose is 200mg per day.
Adolescents aged 13 to 17 years:The recommended starting dose is 50mg per day. The maximum dose is 200mg per day.
If you have liver or kidney problems, inform your doctor and follow the instructions they give you..
Administration form:
Besitran tablets can be taken with or without food.
Take your medication once a day in the morning or at night.
Your doctor will indicate the duration of treatment with this medication. The duration will depend on the nature of your illness and your response to treatment. It will take several weeks for your symptoms to improve. Depression treatment should continue for 6 months after improvement.
If you take more Besitran than you should
If you accidentally take an excess ofBesitran, contact your doctor or go to the nearest hospital emergency service. Always carry the medication packaging with you, whether it is empty or not.
You can also call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
The symptoms of overdose may include drowsiness, nausea and vomiting, rapid heart rate, tremors, agitation, dizziness, and in rare cases, loss of consciousness.
If you forget to take Besitran
Do not take a double dose to compensate for the missed doses. If you forget to take a dose, do not take it when you remember.Take the next dose when it is due.
If you interrupt treatment with Besitran
Do not stop treatment withBesitranunless your doctor tells you to. Your doctor will want to gradually reduce the dose ofBesitranover several weeks before stopping it completely. If you stop treatment abruptly, you may experience side effects such as dizziness, numbness, sleep disturbances, agitation or anxiety, headaches, nausea, vomiting, and tremors. If you experience any of these side effects or any other during the interruption of your treatment withBesitran, please inform your doctor.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication may cause side effects, although not everyone will experience them.
The most common side effect is nausea. Side effects depend on the dose and often disappear or decrease as treatment continues.
Inform your doctor immediately:
If you experience any of the following symptoms after taking this medication, as these symptoms may be serious.
The following side effects were observed in clinical trials in adults and after marketing.
Very common (may affect more than 1 in 10 patients):
Insomnia, dizziness, drowsiness, headache, diarrhea, feeling unwell, dry mouth, ejaculation problems, and fatigue.
Common (may affect up to 1 in 10 patients):
Uncommon (may affect up to 1 in 100 patients):
Rare (may affect up to 1 in 1,000 patients):
Frequency not known: cannot be estimated from available data:
*Side effects reported after marketing.
Other side effects in children and adolescents
In clinical trials in children and adolescents, side effects were generally similar to those reported in adults (see above). The most common side effects in children and adolescents were headache, insomnia, diarrhea, and nausea.
Symptoms that may appear when treatment is stopped
If you stop treatment abruptly, you may experience side effects such asdizziness, numbness, sleep disturbances, agitation or anxiety, headaches, nausea, vomiting, and tremor(see section 3. If you stop treatment with Besitran).
A higher risk of bone fractures has been observed in patients taking this type of medication.
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, 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 Medicinal Products for Human Use:https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keepthis medicationout ofsight and out of reach of children.
Do not usethis medicationafter the expiration date that appears on the packagingafter CAD. The expiration date is the last day of the month indicated.
Do not store at a temperature above 30°C.
Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and unused medicines at the SIGRE collection pointofthepharmacy.If in doubt, ask your pharmacist how to dispose of the packaging and unused medicines. In this way, you will help protect the environment.
The other components are:
calcium dihydroxide phosphate (E341), microcrystalline cellulose (E460), hydroxypropyl cellulose (E463), sodium glycolate starch (type A, from potato),(see section 2 “Besitran contains sodium”), magnesium stearate (E572), hypromellose 2910/3mPas(E464), hypromellose 2910/6 mPas(E464), titanium dioxide (E171), macrogol 400 (E1521), macrogol 8000 (E1521) and polysorbate 80 (E433).
Appearance of the product and contents of the package
Besitran 50 mg is presented in white, film-coated tabletswith a capsule shape (10.3 x 4.2 mm), engraved with “VLE” on one side and “ZLT50”on the other. The tablets can be divided into equal parts.
Besitran is available in blisters containing 10, 14, 15, 20, 28, 30, 50, 56, 60, 84, 98, 100, 200, 294, 300 or 500 tablets, and in blister strips containing 30x1.
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder:
Viatris Healthcare Limited
Damastown Industrial Park
Mulhuddart, Dublin 15
Dublin
Ireland
Manufacturer:
TOWA Pharmaceutical Europe, S.L.
C/ de Sant Martí, 75-97,
Martorelles,
08107 Barcelona,
Spain
or
Pfizer Manufacturing Deutschland GmbH
Mooswaldallee 1?
79108 Freiburg Im Breisgau
Germany
or
Mylan Hungary Kft.
Mylan utca 1
Komárom, 2900
Hungary
Further information on this medicinal product can be obtained by contacting the local representative of the marketing authorization holder:
Viatris Pharmaceuticals, S.L.U.
Calle General Aranaz, 86
28027 Madrid
Spain
This medicinal product is authorized in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names:
Austria | Tresleen |
Belgium, Luxembourg | Serlain |
Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Italy, Latvia, Lithuania, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Sweden | Zoloft |
Ireland, United Kingdom (Northern Ireland) | Lustral |
Spain | Besitran |
Last revision date of this leaflet: March 2025
Further detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/
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