Package Leaflet: Information for the User
Venlabrain Retard 300 mg prolonged-release tablets
venlafaxine
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Venlabrain Retard contains the active substance venlafaxine.
Venlabrain Retard is an antidepressant that belongs to a group of medicines called serotonin and noradrenaline reuptake inhibitors (SNRIs). This group of medicines is used to treat depression and other conditions such as anxiety disorders. It is not fully understood how antidepressants work, but they may help to increase the levels of serotonin and noradrenaline in the brain.
Venlabrain Retard 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 improve or may get worse and become more difficult to treat.
Do not takeVenlabrainRetard
Warnings and precautions
Consult your doctor or pharmacist beforeyou take Venlabrain Retard
Venlabrain Retard may cause a feeling of restlessness or difficulty sitting or standing still during the first few weeks of treatment. You should consult your doctor if this happens to you.
Do not drink alcohol while taking this medicine, as it may cause extreme tiredness and unconsciousness. Taking it with certain medicines and/or alcohol may worsen symptoms of depression and other conditions, such as anxiety disorders.
Thoughts of suicide and worsening of your depression or anxiety disorder
If you are depressed and/or have an anxiety disorder, you may sometimes have thoughts of harming or killing yourself. These thoughts may increase when you first start taking antidepressants, because all these medicines take time to work, usually around 2 weeks, but sometimes longer. These thoughts may also occur when your dose is reduced or when you stop taking Venlabrain Retard.
You are more likely to have these thoughts if:
If you have thoughts of harming or killing yourself at any time, contact your doctor or go to a hospital straight away.
Dry mouth
Dry mouth has been reported in 10% of patients treated with venlafaxine. This may increase the risk of tooth decay. Therefore, you should be careful with your oral hygiene.
Diabetes
Your blood glucose levels may be altered due to Venlabrain Retard. The doses of your diabetes medicines may need to be adjusted.
Sexual problems
Some medicines of the same group as Venlabrain Retard (called SNRIs) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms have persisted after stopping treatment.
Children and adolescents
Venlabrain Retard should not normally be used in the treatment of children and adolescents under 18 years. Also, you should know that in patients under 18 years, there is an increased risk of adverse effects such as suicidal attempts, suicidal thoughts, and hostility (mainly aggression, confrontation, and irritability) when they take this type of medicine. However, your doctor may prescribe this medicine to a patient under 18 years when they decide that it is the best option for the patient. If your doctor has prescribed this medicine to a patient under 18 years and you want to discuss this, please go back to your doctor. You should tell your doctor if any of the above symptoms develop or get worse when these patients under 18 years are taking Venlabrain Retard. Also, the long-term effects of this medicine on safety, growth, maturation, and cognitive and behavioral development have not yet been demonstrated.
Taking Venlabrain Retard with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Your doctor will decide if you can take Venlabrain Retard with other medicines.
Do not start or stop taking any medicines, including those that can be bought without a prescription, herbal remedies, and supplements, before 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, overactive reflexes, diarrhea, coma, nausea, vomiting.
In its most severe form, serotonin syndrome can resemble Neuroleptic Malignant Syndrome (NMS). Signs and symptoms of NMS may include a combination of fever, rapid heartbeat, sweating, severe muscle stiffness, confusion, increased muscle enzymes (measured by a blood test).
If you think you are suffering from serotonin syndrome, inform your doctor immediately or go to the emergency department of your nearest hospital.
You must tell your doctor if you are taking medicines that may affect your heart rhythm.
These include:
The following medicines may also interact with Venlabrain Retard and should be used with caution. It is especially important to tell your doctor or pharmacist if you are taking medicines that contain:
Taking Venlabrain Retard with food, drinks, and alcohol
Venlabrain Retard should be taken with 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 tiredness and unconsciousness, and worsen symptoms of depression and other conditions, such as anxiety disorders.
Pregnancy and breastfeeding
Consult your doctor or pharmacist before taking any medicine.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before taking this medicine. You should only use Venlabrain Retard after discussing the potential benefits and risks to the unborn child with your doctor.
Make sure your doctor and/or midwife know you are taking Venlabrain Retard. When similar medicines (called selective serotonin reuptake inhibitors: SSRIs) are taken during pregnancy, there may be an increased risk that the baby will have a serious condition called persistent pulmonary hypertension of the newborn (PPHN), causing the baby to breathe faster and appear blue. These symptoms usually start during 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, you may have a higher risk of heavy vaginal bleeding after giving birth, especially if you have a history of bleeding disorders. Your doctor or midwife should know you are taking Venlabrain Retard so they can advise you.
If you are taking this medicine during pregnancy, your baby may have problems with breathing, as well as other symptoms that may occur when born, such as not feeding properly. If your baby has these symptoms when born 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, who will decide whether you should stop breastfeeding or stop taking this medicine.
Driving and using machines
Do not drive or use tools or machines until you know how Venlabrain Retard affects you.
Venlabrain Retard contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
Venlabrain Retard contains lactose
If your doctor has told you that you have an intolerance to certain sugars, consult them before taking this medicine.
Take this medicine exactly as your doctor or pharmacist has told you. If you are not sure, ask your doctor or pharmacist.
The usual recommended starting dose for treating depression, generalized anxiety disorder, and social anxiety disorder is 75 mg per day. Your doctor may gradually increase the dose, and if necessary, up to a maximum dose of 375 mg per day for depression.
Take Venlabrain Retard at approximately the same time each day, either in the morning or in the evening.
The tablets should be swallowed whole with liquids and not crushed, chewed, or dissolved.
Venlabrain Retard should be taken with food.
If you have liver or kidney problems, talk to your doctor, as you may need a different dose of this medicine.
Do not stop taking Venlabrain Retard without talking to your doctor (see the section "If you stop taking Venlabrain Retard").
If you have taken more Venlabrain Retard than you should, contact your doctor or pharmacist immediately or go to the emergency department of your nearest hospital. Quote the medicine and the amount taken.
Overdose can be life-threatening, especially when taken with certain other medicines and/or alcohol (see "Taking Venlabrain Retard with other medicines").
Symptoms of a possible overdose may include: palpitations, changes in the level of consciousness (ranging from drowsiness to coma), blurred vision, seizures or fits, and vomiting.
If you miss a dose, take it as soon as you remember. However, if it is already time for your next dose, skip the missed dose and take only a single dose as usual. Do not take a double dose to make up for a forgotten dose. Do not take more than the prescribed daily dose of Venlabrain Retard in one day.
Do not stop taking your treatment or reduce the dose without the advice of your doctor, even if you feel better. If your doctor thinks you no longer need Venlabrain Retard, they may ask you to reduce the dose gradually before stopping treatment completely. It is known that side effects can occur when people stop using this medicine, especially when it is stopped suddenly or the dose is reduced too quickly.
Some patients may experience symptoms such as suicidal thoughts, aggression, tiredness, dizziness, unsteadiness, headache, insomnia, nightmares, dry mouth, loss of appetite, nausea, diarrhea, nervousness, agitation, anxiety, confusion, ringing in the ears, tingling or electric shock-like sensations, weakness, sweating, seizures, or flu-like symptoms, and increased blood pressure (which can cause headache, dizziness, ringing in the ears, sweating, etc.).
Your doctor will advise you on how to gradually stop taking Venlabrain Retard. This may take several weeks or months. In some patients, stopping may need to be done very gradually over several months or longer. If you experience any of these or other symptoms that are troublesome, talk to your doctor for further advice.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
If any of the following effects occur, do not take more Venlabrain Retard. Inform your doctor immediately or go to the nearest hospital:
Uncommon (may affect up to 1 in 100 people)
Rare (may affect up to 1 in 1,000 people)
In its most severe form, serotonin syndrome can resemble Neuroleptic Malignant Syndrome (NMS). Signs and symptoms of NMS may include a combination of fever, tachycardia, sweating, severe muscle stiffness, confusion, increased muscle enzymes (analyzed through a blood test).
Frequency not known (cannot be estimated from available data)
Other adverse effects that you should report to your doctor(the frequency of these adverse effects is included in the list below "other adverse effects that may occur"):
Do not worry if you see a tablet in your stool after taking this medicine. As the tablet passes through the entire gastrointestinal tract, the venlafaxine is released slowly. The structure of the tablet does not dissolve and is eliminated through the stool. Therefore, even if you see a tablet in your stool, the venlafaxine dose has been absorbed.
Other adverse effects that may occur:
Very common (may affect more than 1 in 10 people)
Common (may affect up to 1 in 10 people)
Uncommon (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)
Frequency not known (cannot be estimated from available data)
Venlabrain Retard sometimes produces unwanted effects that you may not be aware of, such as increased blood pressure or an abnormal heartbeat; mild changes in blood levels of liver enzymes, sodium, or cholesterol. Less frequently, Venlabrain Retard may reduce the function of blood platelets, leading to an increased risk of bruising or bleeding. Therefore, your doctor may consider it appropriate to perform occasional blood tests, especially if you have been taking Venlabrain Retard for a long time.
Reporting adverse effects:
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that is not listed in this prospectus. You can also report them directly through the Spanish Pharmacovigilance System for human use medicines: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
This medicine does not require any special storage temperature.
Blister packs: store in the original packaging to protect from moisture.
Plastic bottle: keep the container perfectly closed to protect from moisture.
Medicines should not be thrown down the drain or into the trash. Deposit the packaging and medicines that you no longer need at the Sigre collection point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medicines that you no longer need. This will help protect the environment.
Composition of Venlabrain Retard
The active ingredient is venlafaxine.
Each prolonged-release tablet contains 300 mg of venlafaxine (as hydrochloride).
The other ingredients (excipients) are:
Mannitol (E421), povidone, macrogol, microcrystalline cellulose (E 460(i)), colloidal anhydrous silica, magnesium stearate (E 470b), cellulose acetate, hypromellose, lactose monohydrate, titanium dioxide (E171), and triacetin.
Appearance of the product and packaging content
Prolonged-release tablets 300 mg: white/white tablets, round.
Venlabrain Retard is available in blister packs of 10, 14, 20, 28, 30, 42, 50, 56, 60, 98, 100, and 500 tablets.
Only some pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder:
Exeltis Healthcare, S.L.
Avenida de Miralcampo, 7.
Polígono Industrial Miralcampo.
19200 Azuqueca de Henares. Guadalajara.
Spain.
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 medicine is authorized in the Member States of the European Economic Area under the following names:
Sweden: Venlafaxin Medical Valley 300 mg depottabletter
Denmark: Venlafaxin Medical Valley
Spain: Venlabrain Retard 300 mg prolonged-release tablets
Iceland: Venlafaxin Medical Valley 300 mg forðatöflur
Norway: Venlazid 300 mg
This prospectus was approved in:July 2024
Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
The average price of VENLABRAIN RETARD 300 mg PROLONGED-RELEASE TABLETS in October, 2025 is around 38.31 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.