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Duloxetina ratio 60 mg capsulas duras gastrorresistentes efg

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Introduction

Product Information for the Patient

Duloxetina ratio 30 mg Hard Gastrorresistant Capsules EFG

Duloxetina ratio 60 mg Hard Gastrorresistant Capsules EFG

duloxetina

Read this entire leaflet carefully before you start taking this medicine, as it contains important information for you.

  • Keep this leaflet, as you may need to read it again.
  • If you have any questions, consult your doctor or pharmacist.
  • This medicine has been prescribed for you only and should not be given to others even if they have the same symptoms as you, as it may harm them.
  • If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

1. What is Duloxetina ratio and what is it used for

Duloxetina ratio contains the active ingredient duloxetina. Duloxetina increases the levels of serotonin and noradrenaline in the nervous system.

Duloxetina is used in adults to treat:

  • depression
  • generalized anxiety disorder (chronic feeling of anxiety or nervousness)
  • diabetic neuropathic pain (often described as burning, stabbing, pinching, stinging, or electric shock-like pain. There may be a loss of sensation in the affected area, or pain may occur when touching the area or exposing it to heat, cold, or pressure)

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.

2. What you need to know before taking Duloxetine ratio

Do not take Duloxetina ratio if:

  • You are allergic to duloxetina or any of the other components of this medication (listed in section 6)
  • You have liver insufficiency
  • You have severe kidney insufficiency
  • You are taking or have taken in the last 14 days another medication known as monoamine oxidase inhibitor (MAOI) (see “Taking Duloxetina ratio with other medications”)
  • You are taking fluvoxamine, which is normally used to treat depression, ciprofloxacin or enoxacin, which are used in the treatment of some infections
  • You are taking other medications that contain duloxetina (see “Taking Duloxetina ratio with other medications”)

Consult your doctor if you have high blood pressure or a heart disease. Your doctor will tell you if you should take duloxetina.

Warnings and precautions

Duloxetina may not be suitable for you for the following reasons. Consult your doctor or pharmacist before taking duloxetina if:

  • You are taking other medications to treat depression (see “Taking Duloxetina ratio with other medications”)
  • You are taking St. John's Wort, a herbal treatment (Hypericum perforatum)
  • You have any kidney disease
  • You have had seizures (epileptic attacks)
  • You have had mania
  • You have bipolar disorder
  • You have eye problems, such as some types of glaucoma (increased eye pressure)
  • You have had bleeding problems, especially if you are pregnant (see “Pregnancy and breastfeeding”)
  • You are at risk of having low sodium levels (for example if you are taking diuretics, especially if you are elderly)
  • You are taking other medications that can cause liver damage
  • You are taking other medications that contain duloxetina (see “Taking Duloxetina ratio with other medications”)

Duloxetina may cause a feeling of restlessness or inability to sit or stay still. If this happens, tell your doctor.

Some medications in the group to which duloxetina belongs (called SSRIs/SNRIs) may 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 medications take time to work, usually two weeks but sometimes longer.

It is more likely that you will have these thoughts if:

  • You have had thoughts of self-harm or suicide before
  • You are a young adult. There is information from clinical trials that has shown an increased risk of suicidal behavior in young adults under 25 years old who have a psychiatric disorder and are being treated with antidepressants

Contact your doctor or go directly to the hospital 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 if your depression or anxiety is getting worse, or if they are concerned about changes in your behavior.

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, diarrhea, coma, nausea, vomiting, as you may be suffering from a serotonin syndrome.

In its most severe form, serotonin syndrome may resemble Neuroleptic Malignant Syndrome (NMS). The signs and symptoms of NMS may include a combination of fever, rapid heartbeat, sweating, severe muscle stiffness, confusion, increased muscle enzymes (determined by blood test).

Children and adolescents under 18 years

Duloxetina is normally not used in children and adolescents under 18 years old. You should also know that patients under 18 years old who take this class of medications have an increased risk of developing side effects such as suicidal behavior, suicidal thoughts, and hostility (predominantly aggression, oppositional behavior, and irritability). Despite this, your doctor may prescribe duloxetina to patients under 18 years old because they decide it may be beneficial for the patient. If your doctor has prescribed duloxetina to a patient under 18 years old and you want to talk about it, please go back to your doctor. You should inform your doctor if any of the symptoms above appear or worsen in patients under 18 years old who are taking duloxetina. Additionally, in this age group, the long-term safety effects of duloxetina related to growth, maturation, and cognitive and behavioral development have not yet been demonstrated.

Taking Duloxetina ratio with other medications

Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.

The active ingredient in the medication, duloxetina, is used in other medications for other treatments:

  • Diabetic neuropathic pain, depression, anxiety, and urinary incontinence.

It should be avoided to use more than one of these medications at the same time. Check with your doctor if you are already using other medications that contain duloxetina.

Your doctor will decide if you can take duloxetina with other medications.Do not start or stop using any medication, including those purchased without a prescription and herbal remedies, without first consulting your doctor.

You should also inform your doctor if you are taking any of the following medications:

Monoamine oxidase inhibitors (MAOIs):You should not take duloxetina if you are taking, or have taken in the last 14 days, another medication antidepressant known as monoamine oxidase inhibitor (MAOI). Examples of MAOIs include moclobemide (an antidepressant) and linezolid (an antibiotic). Taking an MAOI with many prescription medications, including duloxetina, may cause serious side effects, even life-threatening. You should wait at least 14 days after stopping treatment with an MAOI before taking duloxetina. Similarly, you should wait at least 5 days after stopping treatment with duloxetina before starting treatment with an MAOI.

Medications that cause drowsiness:This includes prescription medications prescribed by your doctor such as benzodiazepines, powerful analgesics, antipsychotics, phenobarbital, and antihistamines.

Medications that increase serotonin levels:Triptans, tramadol, buprenorphine, tryptophan, selective serotonin reuptake inhibitors (SSRIs, such as paroxetine and fluoxetine), serotonin-norepinephrine reuptake inhibitors (SNRIs, such as venlafaxine), tricyclic antidepressants (such as clomipramine and amitriptyline), petidin, St. John's Wort, and MAOIs (such as moclobemide and linezolid). These medications increase the risk of side effects; if you observe any unusual symptoms when using any of these medications with duloxetina, you should inform your doctor.

Oral anticoagulants or antiplatelet agents:Medications that thin the blood or prevent the formation of blood clots. These medications may increase the risk of bleeding.

Taking Duloxetina ratio with food, drinks, and alcohol

Duloxetina can be taken with or without food. You should be careful if you take alcohol while taking duloxetina.

Pregnancy, breastfeeding, and fertility

If you are pregnant or breastfeeding, or if you think you may be pregnant, consult your doctor or pharmacist before using this medication.

  • Inform your doctor if you become pregnant or if you are trying to become pregnant while taking this medication. You should only use duloxetina after discussing the potential benefits and any potential risks to the fetus with your doctor.
  • Make sure your midwife and/or doctor know that you are taking this medication. Other similar medications (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 duloxetina towards the end of your pregnancy, your baby may have some symptoms when born. These usually start at birth or within the first few days after the baby's birth. These symptoms may include weak muscles, trembling, nervousness, difficulty feeding, breathing problems, and seizures. If your baby has any of these symptoms when born or if you are concerned about your baby's health, contact your doctor or midwife for advice.
  • If you take duloxetina towards the end of your pregnancy, there is a higher risk of excessive vaginal bleeding after birth, especially if you have had bleeding problems. Your doctor or midwife should know that you are taking duloxetina so they can advise you.
  • The available data on the use of duloxetina during the first three months of pregnancy do not show a general increase in the risk of birth defects in the baby. If you take duloxetina during the second half of pregnancy, there may be a higher risk of the baby being born prematurely (six additional premature births per 100 women taking duloxetina in the second half of pregnancy), especially between weeks 35 and 36 of pregnancy.
  • Inform your doctor if you are breastfeeding. Duloxetina is not recommended during breastfeeding. Ask your doctor or pharmacist for advice.

Driving and operating machines

During treatment with duloxetina, you may feel drowsy or dizzy. Do not drive or operate tools or machines until you know how duloxetina affects you.

Duloxetina ratio contains saccharose

If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.

3. How to take Duloxetine ratio

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.

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 usual starting 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.

Duloxetine should be taken orally. You should swallow the capsule whole with water. You can take it with or without food.

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 more Duloxetine ratio than 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 take Duloxetine ratio

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 treatment with Duloxetine ratio

DO NOT stop taking your capsules without your doctor's advice, 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 treatment with duloxetine abruptly have presented symptoms such as:

  • dizziness, feeling of pins and needles or electric shock sensation (especially in the head), sleep disturbances (intense dreams, nightmares, inability to sleep), fatigue, drowsiness, feeling of restlessness or agitation, feeling of anxiety, nausea or vomiting, tremors, headaches, muscle pain, feeling of irritability, diarrhea, and excessive sweating or vertigo.

These symptoms are usually not important 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.

4. Possible Adverse Effects

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)

  • headache, drowsiness.
  • unpleasant feeling (nausea), dry mouth.

Common side effects (may affect up to 1 in 10 patients)

  • loss of appetite.
  • difficulty sleeping, feeling agitated, decreased sex drive, anxiety, difficulty or inability to have an orgasm, unusual dreams.
  • dizziness, feeling slow, tremors, numbness, including numbness, itching, or tingling in the skin.
  • blurred vision.
  • ringing in the ears (perception of sounds in the ear when there is no sound outside).
  • feeling palpitations in the chest.
  • increased blood pressure, flushing.
  • increased yawning.
  • constipation, diarrhea, stomach pain, vomiting, heartburn, or indigestion, gas.
  • increased sweating, rash.
  • muscle pain, muscle spasms.
  • painful urination, urinating frequently.
  • difficulty achieving an erection, changes in ejaculation.
  • falls (mainly in older people), fatigue.
  • weight loss.

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, the weight increased to similar levels as other children and adolescents of the same age and sex.

Uncommon side effects (may affect up to 1 in 100 patients)

  • inflammation of the throat that causes hoarseness.
  • suicidal thoughts, difficulty sleeping, bruxism, feeling disoriented, lack of motivation.
  • muscle spasms and involuntary movements, feeling restless or inability to remain seated or still, nervousness, difficulty concentrating, changes in taste, difficulty controlling movements, e.g., lack of coordination or involuntary muscle movements, restless legs syndrome, poor-quality sleep.
  • pupil dilation (the black center of the eye), vision problems.
  • feeling dizzy or vertigo, ear pain.
  • rapid or irregular heartbeat.
  • loss of consciousness, dizziness, feeling dizzy or loss of consciousness when standing up, cold hands and/or feet.
  • throat spasms, nosebleeds.
  • vomiting blood, or black stools, gastroenteritis, belching, difficulty swallowing.
  • inflammation of the liver that can cause abdominal pain and yellowing of the skin or the white part of the eyes.
  • night sweats, rashes, cold sweats, sensitivity to sunlight, increased tendency to bruise.
  • muscle stiffness, muscle spasms.
  • difficulty or inability to urinate, difficulty starting urination, need to urinate at night, need to urinate more than usual, decreased urine flow.
  • abnormal vaginal bleeding, abnormal menstrual periods, including heavy, painful, irregular, or prolonged periods, occasionally light or absent periods, testicular or scrotal pain.
  • chest pain, feeling cold, thirst, chills, feeling hot, gait disturbance.
  • weight gain.
  • duloxetine may cause effects that you may not be aware of, such as increased liver enzymes or blood levels of potassium, creatine phosphokinase, sugar, or cholesterol.

Rare side effects (may affect up to 1 in 1,000 patients)

  • severe allergic reactions, which cause difficulty breathing or dizziness with swelling of the tongue or lips, allergic reactions.
  • decreased activity of the thyroid gland, which can cause fatigue or weight gain.
  • dehydration, low sodium levels in the blood (mainly in older people; symptoms may include dizziness, weakness, confusion, sleepiness, or excessive fatigue, nausea, or vomiting, more serious symptoms are loss of consciousness, seizures, or falls), syndrome of inappropriate antidiuretic hormone secretion (SIADH).
  • suicidal behavior, mania (hyperactivity, accelerated thinking, and decreased need for sleep), hallucinations, aggression, and anger.
  • "Serotonin syndrome" (a rare reaction that can cause a feeling of intense happiness, drowsiness, clumsiness, restlessness, feeling drunk, fever, sweating, or muscle stiffness), seizures.
  • increased pressure in the eye (glaucoma).
  • cough, wheezing, and shortness of breath, which may be accompanied by high fever.
  • inflammation of the mouth, bright red blood in the stool, bad breath, inflammation of the large intestine (leading to diarrhea)
  • liver failure, yellowing of the skin or the white part of the eyes (jaundice).
  • Stevens-Johnson syndrome (a severe disease with blistering of the skin, mouth, eyes, and genitals), severe allergic reactions that cause swelling of the face or throat (angioedema).
  • jaw muscle contractions.
  • unusual odor of urine.
  • menopausal symptoms, abnormal milk production in men or women.
  • excessive vaginal bleeding shortly after birth (postpartum hemorrhage).

Very rare side effects (may affect up to 1 in 10,000 patients)

  • inflammation of the skin blood vessels (cutaneous vasculitis).

Frequency not known (cannot be estimated from available data)

  • signs and symptoms of a condition called "stress cardiomyopathy," which may include chest pain, difficulty breathing, dizziness, loss of consciousness, and irregular heartbeat.

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 leaflet. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use:www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.

5. Conservation of Duloxetina ratio

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.

Do not store at a temperature above 25°C.

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.

6. Contents of the packaging and additional information

Duloxetina ratio Composition

The active ingredient is duloxetine.

Each capsule contains 30 mg or 60 mg of duloxetine (as hydrochloride).

Theothercomponents are:

Caplet content:sugar spheres (cornstarch and sucrose), hypromellose phthalate, hypromellose, triethyl citrate, hydroxypropyl cellulose, and talc.

30 mg capsule:Hypromellose (E-464), titanium dioxide (E-171), brilliant blue FCF (E-172), iron oxide black (E-172), printing ink.

60 mg capsule:Hypromellose (E-464), titanium dioxide (E-171), iron oxide black (E-172), printing ink.

Printing ink content:shellac, propylene glycol, strong ammonia solution, iron oxide black (E-172), potassium hydroxide.

Product appearance and packaging content

This medicine is a hard, gastro-resistant capsule. Each capsule contains pellets of duloxetine hydrochloride with a coating to protect them from stomach acid.

Duloxetina ratio is available in two doses: 30 mg and 60 mg.

The 30 mg capsules have a grey opaque body with "DLX 30" printed and a blue opaque cap with "DLX 30" printed, length 18 mm.

The 60 mg capsules have a grey opaque body with "DLX 60" printed and a white opaque cap with "DLX 60" printed, length 20 mm.

Duloxetina ratio 30 mg is available in:

  • Plastic bottle (HDPE) with a screw cap with integrated silica gel desiccant of 100 capsules
  • Blister pack (OPA/Al/PVC-Al) in packs of 7, 14, 28, 30, 56, 98, and 100 capsules.

Duloxetina ratio 60 mg is available in:

  • Plastic bottle (HDPE) with a screw cap with a silica gel desiccant integrated of 100 capsules
  • Blister pack (OPA/Al/PVC-Al) in packs of 14, 28, 30, 56, 98, and 100 capsules.

Only some package sizes may be marketed.

Marketing authorization holder and responsible manufacturer

Marketing authorization holder:

Teva Pharma, S.L.U.

C/ Anabel Segura, 11

Edificio Albatros B, 1st floor

28108 Alcobendas, Madrid (Spain)

Responsible manufacturer:

Balkanpharma-Dupnitsa AD

3 Samokovsko Shosse Str.,

Dupnitsa 2600

Bulgaria

Last review date of this leaflet: September 2024

For detailed and updated information on this medicine, please visit the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/.

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Azucar , esferas de (218.76 mg mg), Propilenglicol (1-3 Porcentaje peso/peso mg), Potasio, hidroxido de (e-525) (0.05-0.1 Porcentaje peso/peso mg)
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