Package Insert: Information for the User
Duloxetina pensa pharma 30mg hard gastro-resistant EFG capsules
Duloxetina (hydrochloride)
Read this package insert carefully before starting to take this medication, as it contains important information for you.
Contents of the package and additional information
Duloxetina Pensa Pharmacontains the active ingredient duloxetina. Duloxetina increases the levels of serotonin and noradrenaline in the nervous system.
Duloxetina is used in adults to treat:
Duloxetina begins to take effect in most people with depression or anxiety within two weeks of starting treatment, but it may take between 2 and 4 weeks to start feeling better. Inform your doctor if you do not notice improvement after this time. Your doctor may continue to give you duloxetina when you are feeling better to prevent your depression or anxiety from returning.
In people with diabetic neuropathic pain, it may take several weeks to start feeling better. Consult your doctor if you do not feel better after 2 months.
Do not take Duloxetina Pensa Pharma:
Consult your doctor if you have high blood pressure or a heart condition. Your doctor will tell you if you should take duloxetine.
Warnings and precautions
Duloxetine may not be suitable for you for the following reasons.
Consult your doctor before starting to take this medicine:
You should also contact your doctor:
if you experience signs and symptoms of restlessness, hallucinations, loss of coordination, rapid heartbeat, increased body temperature, rapid changes in blood pressure, hyperactive reflexes, diarrhoea, coma, nausea, vomiting, as you may be suffering from a serotonin syndrome.
In its most severe form, serotonin syndrome can resemble Neuroleptic Malignant Syndrome (NMS). The signs and symptoms of NMS can include a combination of fever, rapid heartbeat, sweating, severe muscle stiffness, confusion, increased muscle enzymes (determined by blood test).
Duloxetine Pensa Pharma may cause a feeling of restlessness or inability to sit or stay still. If this happens, you should tell your doctor.
Some medicines in the same group as Duloxetine Pensa Pharma (called SSRIs/SNRIs) can cause sexual dysfunction symptoms (see section 4.). In some cases, these symptoms persist after stopping treatment.
Thoughts of suicide and worsening of depression or anxiety
If you are depressed and/or have anxiety disorders, you may occasionally have thoughts of self-harm or suicide. These thoughts may be increased at the beginning of treatment with antidepressants, as all these medicines take time to work, usually two weeks but sometimes longer.
You are more likely to have these thoughts if:
Contact your doctor or go directly to the hospital immediately if you have any thoughts of self-harm or suicide.
It may be helpful to tell a close friend or family member that you are depressed or have an anxiety disorder, and ask them to read this leaflet. They may be able to tell you if your depression or anxiety is getting worse, or if they are concerned about changes in your behaviour.
Children and adolescents
Duloxetine should not normally be used in children and adolescents under 18 years of age. You should also know that patients under 18 years of age who take this class of medicines have an increased risk of side effects such as suicidal thoughts, suicidal behaviour and hostility (mainly aggression, oppositional behaviour and irritability). Despite this, your doctor may prescribe duloxetine for patients under 18 years of age because they decide it may be beneficial for the patient. If your doctor has prescribed duloxetine for a patient under 18 years of age and you want to talk about it, please go back to the doctor. You should tell your doctor if any of the symptoms mentioned above appear or get worse in patients under 18 years of age who are taking duloxetine. Also, in this age group, the long-term safety effects of duloxetine related to growth, maturation and development of cognitive and behavioural functions have not yet been demonstrated.
Other medicines and Duloxetine Pensa Pharma
Inform your doctor or pharmacist if you are using, have used recently or may need to take any other medicine, even those bought without a prescription.
The main component of Duloxetine Pensa Pharma, duloxetine, is used in other medicines for other treatments:
You should avoid using more than one of these medicines at the same time. Check with your doctor if you are already using other medicines that contain duloxetine.
Your doctor will decide if you can take duloxetine with other medicines.Do not start or stop taking any medicine, including those bought without a prescription and herbal remedies, without first consulting your doctor.
You should also tell your doctor if you are taking any of the following medicines:
Monamine oxidase inhibitors (MAOIs):You should not take duloxetine if you are taking, or have taken in the last 14 days, another antidepressant known as a monoamine oxidase inhibitor (MAOI). For example, moclobemide (an antidepressant) and linezolid (an antibiotic). Taking a MAOI with many prescription medicines, including duloxetine, can cause serious side effects, even life-threatening. You should wait at least 14 days after stopping treatment with a MAOI before taking duloxetine. Similarly, you should wait at least 5 days after stopping treatment with duloxetine before starting treatment with a MAOI.
Medicines that cause drowsiness:This includes prescription medicines such as benzodiazepines, strong analgesics, antipsychotics, phenobarbital and antihistamines.
Medicines that increase serotonin levels:Triptans, tramadol, tryptophan, selective serotonin reuptake inhibitors (SSRIs, such as paroxetine and fluoxetine), serotonin-norepinephrine reuptake inhibitors (SNRIs, such as venlafaxine), tricyclic antidepressants (such as clomipramine, amitriptyline), petidina, St. John's Wort and MAOIs (such as moclobemide and linezolid). These medicines increase the risk of side effects; if you notice any unusual symptoms when using any of these medicines with duloxetine, you should tell your doctor.
Oral anticoagulants or antiplatelet agents:Medicines that thin the blood or prevent the formation of blood clots. These medicines may increase the risk of bleeding.
Taking Duloxetine Pensa Pharma with food, drinks and alcohol
Duloxetine can be taken with or without food. You should be careful if you take alcohol while taking duloxetine.
Pregnancy, breastfeeding and fertility
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medicine.
Make sure your midwife and/or doctor know that you are taking duloxetine. Other similar medicines (SSRIs), taken during pregnancy, may increase the risk of a serious condition in babies, called persistent pulmonary hypertension of the newborn (PPHN), which makes the baby breathe more rapidly and turn blue. These symptoms usually start within the first 24 hours after the baby's birth. If this happens to your baby, you should contact your midwife and/or doctor immediately.
If you take duloxetine towards the end of your pregnancy, your baby may have some symptoms when it is born. These usually start at the time of birth or within the first few days after the baby's birth. These symptoms may include weak muscles, trembling, nervousness, the baby not feeding properly, breathing problems and convulsions. If your baby has any of these symptoms when it is born or if you are concerned about your baby's health, contact your doctor or midwife, who can advise you.
Driving and operating machinery
During treatment with duloxetine, you may feel drowsy or dizzy. Do not drive or operate tools or machinery until you know how duloxetine affects you.
Duloxetine Pensa Pharma contains saccharose
Duloxetine contains saccharose. If your doctor has told you that you have an intolerance to certain sugars, consult them before taking this medicine.
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.
Duloxetine should be taken orally. Swallow the capsule whole with water.
For depression and diabetic neuropathic pain:
The recommended dose of duloxetine is 60 mg once a day, but your doctor will prescribe the dose that is best for you.
For generalized anxiety disorder:
The initial normal dose of duloxetine is 30 mg once a day, after which most patients will receive 60 mg once a day, but your doctor will prescribe the dose that is best for you. The dose can be adjusted to 120 mg per day depending on your response to duloxetine.
To avoid forgetting to take duloxetine, it may be helpful to take it at the same time every day.
Discuss with your doctor for how long you should take duloxetine. Do not stop taking duloxetine, or change your dose without consulting your doctor. It is essential to treat your condition properly to help you improve. If you do not treat it, your condition may not disappear and may become more severe and harder to treat.
If you take moreDuloxetine Pensa Pharmathan you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20 indicating the medication and the amount ingested.
Among the symptoms produced by an overdose are drowsiness, coma, serotonin syndrome (a rare reaction that can cause a feeling of intense happiness, drowsiness, clumsiness, restlessness, feeling drunk, fever, sweating, or muscle rigidity) seizures, vomiting, and high heart rate.
If you forgot to takeDuloxetine Pensa Pharma
If you forget to take a dose, take it as soon as you remember. However, if it is time for the next dose, skip the missed dose and take a single dose as you normally do. Do not take a double dose to compensate for the missed doses. Do not take more duloxetine than prescribed for you in a day.
If you interrupt the treatment withDuloxetine Pensa Pharma
DO NOT stop taking your capsules without consulting your doctor, even if you feel better. If your doctor thinks you no longer need to take duloxetine, they will instruct you to reduce your dose for at least 2 weeks before stopping treatment.
Some patients who have stopped taking duloxetine abruptly have experienced symptoms such as:
These symptoms are usually not significant and disappear within a few days, but if you have symptoms that are bothersome, ask your doctor for advice.
If you have any other doubts 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.
These side effects are usually mild to moderate and often disappear within a few weeks.
Very common side effects (may affect more than 1 in 10 patients)
Common side effects (may affect up to 1 in 10 patients)
Children and adolescents under 18 years of age with depression treated with this medicine experienced a decrease in weight when they started taking this medicine. After 6 months of treatment, their weight levels were similar to those of other children and adolescents of the same age and sex.
Uncommon side effects (may affect up to 1 in 100 patients)
Rare side effects (may affect up to 1 in 1,000 patients)
Very rare side effects (may affect 1 in 10,000 patients)
Frequency not known (cannot be estimated from available data)
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 prospectus. You can also report them directly through the Spanish System for the Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es. By reporting side effects, 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. The expiration date is the last day of the month indicated.
PVC-PVDC/Alu Blister: Store below 30°C. Store in the original packaging to protect it from moisture. Store the blister in the outer packaging to protect it from light.
Alu/Alu Blister:This medication does not require any special storage temperature.Store in the original packaging to protect it from light and moisture.
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 ofDuloxetina Pensa Pharma
Theactive ingredientis duloxetina.Each capsule contains30 mg of duloxetina (as hydrochloride).
Theothercomponents are:
Appearance of the product and content of the container
Duloxetina Pensa Pharma is a hard, gastro-resistant capsule. The capsules are blue and white, printed with black ink.
Duloxetina Pensa Pharma 30 mg is available in blisters of 7, 28 and 504 capsules.
Only some package sizes may be marketed.
Holder of the marketing authorization and responsible manufacturer
Holder of the marketing authorization:
Towa Pharmaceutical, S.A.
C/ de Sant Martí, 75-97
08107 Martorelles (Barcelona)
Spain
Responsible manufacturer:
Towa Pharmaceutical Europe, S.L.
C/ de Sant Martí 75-97
08107 Martorelles (Barcelona)
Spain
Last review date of this leaflet:June 2024
Detailed information on 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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