Package Leaflet: Information for the User
Altisben 50 mg Film-Coated Tablets
sertralina
Read this leaflet carefully before you start taking this medicine because it contains important information for you.
Altisben contains sertraline as the active ingredient. Sertraline belongs to a group of medications called Selective Serotonin Reuptake Inhibitors (SSRIs); these medications are used to treat depression and/or anxiety disorders.
Altisben can 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 diseases linked to anxiety, with symptoms such as being constantly preoccupied with repeated ideas (obsessions) that lead to repetitive rituals.
PTSD is a disorder that can occur after a very emotionally traumatic experience, and has some symptoms similar to depression and anxiety. Social anxiety disorder (social phobia) is an anxiety disorder. 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 that this medication is suitable for treating your disease.
If you are unsure why you have been prescribed Altisben, you should consult your doctor.
Do not take Altisben:
Warnings and precautions
Consult your doctor or pharmacist before starting to take Altisben.
Medications are not always suitable for everyone. Before starting treatment with Altisben, tell your doctor if you have or have had any of the following conditions:
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 Altisben 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 depression or anxiety
If you are depressed and/or have anxiety disorders, you may have thoughts of harming yourself or suicidal thoughts. 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 can be longer.
This is more likely to happen
If you have thoughts of harming yourself or suicidal thoughts 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 an anxiety disorder, 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.
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Sexual problems
Some medications in the group to which Altisben 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). Children and adolescents under 18 years old have a higher risk of side effects such as suicidal thoughts, thoughts of self-harm, or suicidal behavior (suicidal ideation) and hostility (predominantly aggression, confrontational behavior, and irritable reaction) when treated with this class of medications. However, it is possible that your doctor may decide to prescribe Altisben 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 Altisben 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 while you are taking Altisben. The long-term effects on safety and related to growth, maturity, and learning (cognitive development) and behavioral development of Altisben 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 Altisben
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 Altisben works, or Altisben itself may reduce the effectiveness of other medications you are taking at the same time.
The use of Altisben with the following medications may cause serious side effects:
Inform your doctor if you are taking the following medications:
The effects of St. John's Wort may last 1-2 weeks.
Altisben with food, drinks, and alcohol:
Altisben tablets can be taken with or without food.
Avoid drinking alcohol while being treated with Altisben.
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, consult your doctor or pharmacist before using this medication.
The safety of sertraline in pregnant women has not been fully established. If you are pregnant, sertraline will only be administered to you if your doctor considers that the benefits for you outweigh any possible risk to the developing fetus.
If you take Altisben in the final stages of pregnancy, there may be an increased risk of excessive vaginal bleeding after delivery, especially if you have a history of bleeding disorders. Your doctor or midwife should know that you are taking sertraline so that they can advise you.
When taken during pregnancy, especially during the last three months of pregnancy, medications like Altisben may increase the risk of a serious condition in newborns called persistent pulmonary hypertension of the newborn (PPHN), which makes the baby 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 that 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 who are 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 the quality of sperm. 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.
Altisben contains sodium:
This medication contains less than 23 mg of sodium (1 mmol) per tablet; it is essentially "sodium-free".
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended dose is:
Adults:
Depression and Obsessive-Compulsive Disorder:
The commonly effective dose for depression and OCD is 50 mg per day. The daily dose can be increased by 50 mg at intervals of at least one week, and thus for several weeks. The maximum recommended dose is 200 mg 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 start with a dose of 25 mg per day, and increased to 50 mg per day after one week.
The daily dose can be increased at intervals of 50 mg over a period of several weeks. The maximum recommended dose is 200 mg per day.
Use in children and adolescents:
Altisben 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 25 mg per day. After one week, your doctor may increase the dose to 50 mg per day. The maximum dose is 200 mg per day.
Adolescents aged 13 to 17 years:The recommended starting dose is 50 mg per day. The maximum dose is 200 mg per day.
If you have liver or kidney problems, inform your doctor and follow the instructions they give you..
Administration form:
Altisben tablets can be taken with or without food.
Take your medication once a day, either 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 may take several weeks for your symptoms to improve.The treatment of depression usually should continue for 6 months after improvement.
If you take more Altisben than you should
If you accidentally take an excessive amount of Altisben, contact your doctor or go to the nearest hospital emergency service. Always carry the medication packaging with you, whether it contains medication or not.
You can also call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
The symptoms of overdose may include drowsiness, nausea, vomiting, rapid heart rate, tremors, agitation, dizziness, and in rare cases, unconsciousness.
If you forget to take Altisben
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 Altisben
Do not interrupt treatment with Altisben unless your doctor tells you to. Your doctor will want to gradually reduce the dose of Altisben over several weeks before stopping treatment 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 with Altisben, please inform your doctor.
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.
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 medicine, as these symptoms can 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):
- cold (chest), sore throat, coughing,
- loss of appetite, increased appetite,
- anxiety, depression, agitation, decreased libido, nervousness, feeling strange, nightmares, teeth grinding,
- tremors, muscle movement problems (such as constant movements, muscle tension, difficulty walking, and stiffness, spasms, and involuntary muscle movements)*, numbness and tingling, increased muscle tone, lack of concentration, abnormal taste,
- visual disturbances,
- ringing in the ears,
- palpitations,
- hot flashes,
- yawning,
- stomach discomfort, constipation, abdominal pain, vomiting, gas,
- increased sweating, rash,
- back pain, joint pain, muscle pain,
- irregular menstrual cycle, erectile dysfunction,
- feeling unwell, chest pain, weakness, fever,
- weight gain,
- injury.
Uncommon (may affect up to 1 in 100 patients):
- gastroenteritis, ear infection,
- tumor,
- hypersensitivity, seasonal allergy,
- low thyroid hormone levels,
- suicidal thoughts, suicidal behavior*, psychotic disorders, abnormal thoughts, neglect, hallucinations, aggression, excessive happiness, paranoia,
- amnesia, decreased sensitivity, involuntary muscle contractions, fainting, continuous movements, migraine, convulsions, dizziness when standing, abnormal coordination, speech disorders,
- dilated pupils,
- ear pain,
- rapid pulse, heart problems,
- bleeding problems (such as stomach bleeding)*, high blood pressure, hot flashes, blood in urine,
- shortness of breath, nasal bleeding, possible noisy breathing,
- black stools, dental problems, esophageal inflammation, tongue problems, hemorrhoids, excessive salivation, difficulty swallowing, belching, tongue disorders,
- eye swelling, urticaria, hair loss, itching, purple spots on the skin, skin problems with blisters, dry skin, facial swelling, cold sweat,
- arthritis, muscle spasms, muscle cramps*, muscle weakness,
- increased frequency of urination, urinary problems, urinary retention, incontinence, increased urine volume, nocturia,
- sexual dysfunction, excessive vaginal bleeding, vaginal bleeding, female sexual dysfunction,
- swollen legs, chills, difficulty walking, thirst,
- increased liver enzyme levels, weight loss,
-There have been reports of suicidal thoughts and behavior during treatment with sertraline or shortly after stopping treatment (see section 2).
Rare (may affect up to 1 in 1,000 patients):
- diverticulitis, lymph node swelling, low platelet count*, low white blood cell count*,
- severe allergic reaction,
- endocrine problems*,
- high cholesterol, difficulty controlling blood sugar levels (diabetes), low blood sugar, high blood sugar*, low sodium levels*,
- physical symptoms due to stress or emotions, abnormal nightmares*, medication dependence, sleepwalking, premature ejaculation,
- coma, abnormal movements, difficulty moving, increased sensitivity, severe headache (which may be a sign of a serious condition known as reversible cerebral vasoconstriction syndrome (RCVS))*, sensory disturbances,
- spots in front of the eyes, glaucoma, double vision, photophobia (light sensitivity), eye bleeding, irregular pupils*, visual disturbances*, eye problems,
- heart attack, dizziness, fainting, or chest pain that may be signs of changes in electrical activity (seen on the electrocardiogram) or abnormal heart rhythm*, decreased heart rate,
- circulation problems in the arms and legs,
- rapid breathing, progressive scarring of lung tissue (interstitial lung disease)*, throat spasm, difficulty speaking, slower breathing, hiccups,
- a type of lung disease in which eosinophils (a type of white blood cell) appear in the lungs in large numbers (eosinophilic pneumonia),
- mouth ulcers, pancreatitis*, blood in stool, tongue ulcers, mouth sores,
- liver function problems, severe liver function problems*, yellow skin and eyes (jaundice)*,
- sunburn reaction*, skin swelling*, abnormal hair texture, abnormal skin odor, capillary eruption,
- muscle tissue rupture*, bone disorders,
- interrupted urination, decreased urine volume,
- nipple secretion, vaginal dryness, genital secretion, penile and preputial pain and redness, breast enlargement*, prolonged erection,
- hernia, decreased tolerance to the medication,
- increased cholesterol levels, abnormal analytical results*, abnormal semen, coagulation problems*,
- vasodilation relaxation.
Frequency not known (cannot be estimated from available data):
- mandibular blockage*,
- nocturia*,
- partial loss of vision,
- colitis inflammation (which causes diarrhea)*,
- excessive postpartum vaginal bleeding (postpartum hemorrhage), see “Pregnancy, lactation, and fertility” in section 2 for more information.
*Adverse reactions reported after marketing.
Other adverse reactions in children and adolescents
In clinical trials in children and adolescents, adverse reactions were generally similar to those reported in adults (see above). The most common adverse reactions in children and adolescents were headache, insomnia, diarrhea, and nausea.
Symptoms that may appear when treatment is stopped
If you stop treatment with this medicine abruptly, you may experience side effects such as dizziness, numbness, sleep disturbances, agitation or anxiety, headaches, nausea, vomiting, and tremors (see section 3. If you stop treatment with this medicine).
There has been an increased risk of bone fractures in patients taking this type of medication.
Reporting of adverse reactions
If you experience any type of adverse reaction, consult your doctor, pharmacist, or nurse, even if it is a possible adverse reaction that does not appear in this leaflet. You can also report them directly throughSistema Español de Farmacovigilancia de Medicamentos de Uso Humano:https://www.notificaram.es. By reporting adverse reactions, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging, after CAD. The expiration date is the last day of the month indicated.
No special storage conditions are required.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Altisben
The active ingredient of Altisben 50 mg is sertraline (hydrochloride). Each tablet contains 50 mg of sertraline.
The other components are:
Tablet core: calcium phosphate dibasic dihydrate, microcrystalline cellulose, sodium carboxymethylcellulose from potato, magnesium stearate, hydroxypropylcellulose.
Tablet coating: hypromellose, titanium dioxide (E171) and triacetin (E422).
Appearance of the product and content of the packaging
Altisben 50 mg is presented in film-coated tablets, round, lenticular, white, scored. It is presented in blisters, in packs of 30 tablets.
Holder of the marketing authorization and responsible for manufacturing
Laboratorios Alter, S.A.
Mateo Inurria, 30
28036 Madrid
Spain
Date of the last review of this leaflet:May 2024
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/
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