Product Information for the User
Venlabrain Retard 150 mg prolonged-release tablets
venlafaxine
Read this entire product information carefully before starting to take this medicine, as it contains important information for you.
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Venlabrain Retard contains the active ingredient venlafaxine.
VenlabrainRetardis an antidepressant that belongs to a group of medications called serotonin and noradrenaline reuptake inhibitors (SNRIs). This group of medications is used to treat depression and other conditions such as anxiety disorders.The exact mechanism of action of antidepressants is not fully understood, but they may help increase levels of serotonin and noradrenaline in the brain.
VenlabrainRetard is a treatment for adults with depression. It is also a treatment for adults with the following anxiety disorders: generalized anxiety disorder, social anxiety disorder (fear or avoidance of social situations), panic disorder (panic attacks). Treating depressive and anxiety disorders properly is important to help you feel better. If left untreated, your condition may not go away or may worsen and become harder to treat.
-If you are allergic to venlafaxine or any of the other ingredients in this medicine (see section 6).
-If you are also taking or have taken in the last 14 days, any medicine known as an irreversible monoamine oxidase inhibitor (IMAO) used to treat depression or Parkinson's disease. Taking an IMAO irreversible withVenlabrainRetard may cause serious or potentially life-threatening side effects. You should also wait at least 7 days after stoppingVenlabrainRetard before taking any IMAO irreversible (see also the section “Taking Venlabrain Retard with other medicines” and the information in this section on Serotonin Syndrome).
Warnings and precautions
Consult your doctor or pharmacistbeforestarting to take Venlabrain Retard
VenlabrainRetard may cause restlessness or difficulty sitting or staying still during the first few weeks of treatment. You should consult your doctor if this happens.
Do not drink alcohol during treatment with this medicine, as it may cause extreme drowsiness and loss of consciousness. Taking it with certain medicines and/or alcohol may worsen the symptoms of depression and other conditions, such as anxiety disorders.
Thoughts of suicide and worsening of depression or anxiety disorder
If you are depressed and/or have an anxiety disorder, you may sometimes have thoughts of harming yourself or suicide. These thoughts may also increase when you start taking antidepressants, as all these medicines take time to work, usually two weeks, but sometimes longer. These thoughts may occur when your dose is reduced or during the interruption of treatment with Venlabrain Retard.
It is more likely that you will have these thoughts in the following situations:
-If you have had thoughts of suicide or self-harm before.
-If you are a young adult. Clinical trial information has shown an increased risk of suicidal behaviour in young adults (less than 25 years old) with psychiatric illnesses treated with antidepressants.
If you have thoughts of harming yourself or suicide at any time, contact your doctor or go to the hospital immediately.
You may find it helpful to tell a close relative or friend that you are depressed or have an anxiety disorder, and ask them to read this leaflet. You may 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 behaviour.
Dry mouth
Dry mouth has been reported in 10% of patients treated with venlafaxine. This may
increase the risk of tooth decay. You should take good care of your oral hygiene.
Diabetes
Your blood glucose levels may be affected byVenlabrainRetard, and you may need to adjust your diabetes medicines.
Sexual problems:
Medicines like Venlabrain Retard (also known as SSRIs) may cause sexual side effects (see section 4). In some cases, these side effects may continue even after you have stopped taking the medicine.
Children and adolescents
Venlabrain Retard should not normally be used to treat children and adolescents under 18 years old.Also, you should know that inpatients under 18 years old, there is a higher risk of side effects such as suicidal thoughts, suicidal behaviour, and hostility (mainly aggression, confrontational behaviour, and irritability) when taking this type of medicine.Your doctor may prescribe this medicine to a patient under 18 years old if they decide it is the best option for the patient.If your doctor has prescribed this medicine to a patient under 18 years old and you want to discuss this decision, please go back to your doctor. You should tell your doctor if any of the symptoms listed above develop or worsen in these patients under 18 years old who are taking Venlabrain Retard. Also, the long-term effects of this medicine on growth, maturation, and cognitive and behavioural development have not yet been demonstrated.
Taking Venlabrain Retard with other medicines
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medicine.
Your doctor will decide if you can take Venlabrain Retard with other medicines.
Do not start or stop taking any medicine, including those available over the counter, natural remedies, and herbal products, without checking with your doctor or pharmacist.
Examples of these medicines include:
The signs and symptoms of Serotonin Syndrome may include a combination of the following:restlessness, hallucinations, loss of coordination, rapid heartbeat, increased body temperature, rapid changes in blood pressure, hyperactive reflexes, diarrhoea, coma, nausea, and vomiting.
In its most severe form, Serotonin Syndrome may resemble Neuroleptic Malignant Syndrome (NMS). Signs and symptoms of NMS may include a combination of fever, rapid heartbeat, sweating, severe muscle stiffness, confusion, and increased muscle enzymes (detected by a blood test).
If you think you are suffering from Serotonin Syndrome, inform your doctor immediately or go to the hospital emergency department.
You should inform your doctor if you are taking medicines that may affect your heart rhythm.
Examples of these medicines include:
The following medicines may interact withVenlabrainRetard and should be used with caution. It is especially important to inform your doctor or pharmacist if you are taking medicines that contain:
Taking Venlabrain Retard with food, drinks, and alcohol
VenlabrainRetard should be takenwith food (see section 4.3 “How to take Venlabrain Retard”).Do not drink alcohol during treatment with this medicine. Taking it with alcohol may cause extreme drowsiness and loss of consciousness, and may worsen the symptoms of depression and other conditions, such as anxiety disorders.
Pregnancy and breastfeeding
Consult your doctor or pharmacist before using any medicine.
If you are pregnant or breastfeeding, or think you may be pregnant, or are planning to become pregnant, consult your doctor or pharmacist before using this medicine.You should only useVenlabrainRetard after discussing the possible benefits and risks for the unborn baby with your doctor.
Make sure your doctor and/or midwife know that you are takingVenlabrainRetard. When taking similar medicines (called selective serotonin reuptake inhibitors: SSRIs) during pregnancy, there may be an increased risk of a serious condition called persistent pulmonary hypertension of the newborn (PPHN), causing 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, you should contact your doctor and/or midwife immediately.
If you take Venlabrain Retard in the final stages of pregnancy, there may be an increased risk of heavy vaginal bleeding after delivery, especially if you have a history of bleeding disorders. Your doctor or midwife should know that you are taking Venlabrain Retard so they can advise you.
If you are taking this medicine during pregnancy, your baby may have problems breathing, as well as another symptom that may occur at birth, such as not feeding properly. If your baby has these symptoms at birth and you are concerned, contact your doctor and/or midwife, who will be able to advise you.
Venlabrain Retard passes into breast milk.There is a risk of an effect on the baby, so you should discuss this with your doctor and they will decide whether you should stop breastfeeding or stop taking this medicine.
Driving and using machines
Do not drive or operate machinery until you know how Venlabrain Retard affects you.
Venlabrain Retard contains lactose
If your doctor has told you that you have a rare hereditary problem of galactose intolerance, consult your doctor before taking this medicine.
The normal initial recommended dose for the treatment of depression, generalized anxiety disorder, and social anxiety disorder is 75 mg per day. Your doctor may gradually increase the dose and, if necessary, further to a maximum dose of 375 mg per day for depression. If you are being treated for panic disorder, your doctor will start with a lower dose (37.5 mg) and then gradually increase the dose. The maximum dose for generalized anxiety disorder, social anxiety disorder, and panic disorder is 225 mg/day.
Take Venlabrain Retard approximately at the same time every day, either in the morning or at night.
The tablets should be swallowed whole with liquids and should not be crushed, chewed, or dissolved.
Venlabrain Retard should be taken with food.
If you have liver or kidney problems, talk to your doctor as your dose of this medication may need to be different.
Do not stop taking Venlabrain Retard without consulting your doctor (see section “If you interrupt treatment with Venlabrain Retard”).
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.
Overdose can put your life at risk, especially with the simultaneous intake of certain medications and/or alcohol (see Taking Venlabrain Retard with other medications).
The symptoms of a possible overdose may include: palpitations, changes in level of alertness (ranging from drowsiness to coma), blurred vision, convulsions or seizures, and vomiting.
If a dose has not been taken, take it as soon as you remember. However, if it is already time for your next dose, skip the missed dose and take only one dose as usual.Do not take a double dose to compensate for the missed doses.Do not take more than the daily dose of Venlabrain Retard that has been prescribed for you in a day.
Do not stop taking your treatment or reduce the dose without consulting your doctor, even if you feel better. If your doctor believes that you no longer need Venlabrain Retard, they may ask you to gradually reduce the dose before stopping treatment completely. It is known that adverse effects occur when people stop using this medication, especially when it is stopped suddenly or if the dose is reduced very quickly.
Some patients may experience symptoms such as suicidal thoughts, aggression, fatigue, dizziness, lack of stability, headaches, insomnia, nightmares, dry mouth, loss of appetite, nausea, diarrhea, nervousness, agitation, anxiety, confusion, tinnitus, tingling or electric shock sensations in rare cases, weakness, sweating, convulsions, or symptoms similar to the flu, vision problems, and increased blood pressure (which can cause headaches, dizziness, ringing in the ears, sweating, etc.).
Your doctor will advise you on how to gradually stop treatment with Venlabrain Retard. This may take several weeks or months. In some patients, the interruption may need to be produced very gradually over months or more.If you experience any of these or other symptoms that bother you, consult your doctor for further advice.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
If any of the following side effects occur, do not take moreVenlabrainRetard. Inform your doctor immediately or go to the nearest hospital:
Rare (may affect up to 1 in 100 people)
Uncommon (may affect up to 1 in 1,000 people)
In its most severe form, serotonin syndrome may resemble Malignant Neuroleptic Syndrome (MNS). Signs and symptoms of MNS may include a combination of fever, rapid heart rate, sweating, severe muscle rigidity, confusion, and increased muscle enzymes (detected through blood tests).
-Signs of infection, such as fever, chills, shivering, headache, sweating, or symptoms similar to the flu. This may be due to a blood disorder that can increase the risk of infection.
-Severe rash, which may lead to the formation of severe blisters and skin peeling.
-Mysterious muscle pain, discomfort, or weakness. This may be a sign of rhabdomyolysis.
Unknown frequency (cannot be estimated from available data)
Other side effects that you shouldinform your doctor(the frequency of these side effects are included in the list below "other side effects that may occur"):
Do not worry if you see a tablet in your stool after taking this medication. As the tablet passes through the entire gastrointestinal tract, the venlafaxine is released slowly. The tablet structure does not dissolve and is eliminated through the stool. Therefore, although you may observe a tablet in the stool, the venlafaxine dose has been absorbed.
Other side effects that may occur:
Very common (may affect more than 1 in 10 people)
Common (may affect up to 1 in 10 people)
Rare (may affect up to 1 in 100 people).
Rare (may affect up to 1 in 1,000 people).
Very rare (may affect up to 1 in 10,000 people)
Unknown frequency (cannot be estimated from available data)
VenlabrainRetardmay sometimes cause unwanted effects that you may not be aware of, such as increased blood pressure or abnormal heart rhythm; mild changes in liver enzyme levels, sodium, or cholesterol. Less frequently, VenlabrainRetardmay reduce blood platelet function, leading to an increased risk of petechiae or bleeding. Therefore, your doctor may consider it appropriate to perform occasional blood tests, particularly if you have been taking VenlabrainRetardfor a long time.
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 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 medication.
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.
This medication does not require any special temperature for conservation.
Blister packs: store in the original packaging to protect from moisture.
Plastic bottle: keep the packaging perfectly closed to protect from moisture.
Medications should not be disposed of through drains or trash.Deposit the packaging and medications you no longer need at the pharmacy's Sigre Point. In case of doubtask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition ofVenlabrainRetard
The active ingredient is venlafaxine.
Each prolonged-release tablet contains 150 mg of venlafaxine (as hydrochloride).
The other components (excipients) are:
Core: mannitol (E421), povidone K-90, macrogol 400, microcrystalline cellulose(E 460(i)), anhydrous colloidal silica, magnesium stearate(E 470b).
Coating: cellulose acetate, macrogol 400, hypromellose, lactose monohydrate, titanium dioxide (E171) and triacetin.
Appearance of the product and contents of the package
Prolonged-release tablets 150 mg: white to off-white colored, round, biconvex tablets with a diameter of 9.5 mm and a small mark on one side.
Venlabrainretard 150 mg is available in blisters of10, 14, 20, 28, 30,42, 50, 56, 60, 100 and 500 tablets and in plastic bottles of 10, 14, 20, 28, 30, 50, 56, 60, 100, 105, 106, 110 and 500 tablets.
Only some package sizes may be marketed.
Marketing authorization holder and responsible manufacturer
Marketing authorization holder:
Exeltis Healthcare, S.L.
Avenida de Miralcampo, 7.
Polígono Industrial Miralcampo.
19200 Azuqueca de Henares. Guadalajara.
Spain.
Responsible manufacturer:
Laboratorios LICONSA, S.A.
Avda.Miralcampo, Nº 7, Polígono Industrial Miralcampo
19200 Azuqueca de Henares (Guadalajara), Spain
or
Winthrop Arzeinmittel GmbH
Brüningstraße 50
65926 Frankfurt am Main
Germany
This medicinal product is authorized in the Member States of the European Economic Area with the following names:
Sweden: Venlafaxin Medical Valley 75/150/225 mg depot tablets
Germany: Venlafaxin Winthrop® osmo 75/150/225 mg Retard tablets
Denmark: Venlafaxin Medical Valley
Spain:VenlabrainRetard 75/150/225 mg prolonged-release tablets
Iceland: Venlafaxin Medical Valley 75/150/225 mg forðatöflur
Norway: Venlazid 75/150/225 mg
Last review date of this leaflet:July 2024
Detailed information about this medicinal product is available on the website of the Spanish Agency of Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/
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