Dobupal 75 mg tablets
venlafaxine
Dobupal is an antidepressant that belongs to a group of medicines called serotonin and norepinephrine 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 norepinephrine in the brain.
Dobupal is a treatment for adults with depression. Treating depressive disorders adequately is important to help you feel better. If left untreated, your condition may not disappear or may worsen and become more difficult to treat.
Consult your doctor or pharmacist before starting to take Dobupal:
Dobupal 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.
Some medicines in the same group as Dobupal (called SSRIs/SNRIs) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms persist after stopping treatment.
Do not drink alcohol during treatment with Dobupal, as it may cause extreme fatigue and unconsciousness. Taking it with certain medicines and/or alcohol may worsen the symptoms of depression and other conditions, such as anxiety disorders.
If you are depressed and/or have an anxiety disorder, you may sometimes have thoughts of harming yourself or suicide. These thoughts may increase when you first start taking antidepressants, as all these medicines take time to work, usually about two weeks, but sometimes longer. These thoughts may also occur when your dose is reduced or during the interruption of treatment with Dobupal.
It is more likely to happen to you:
If you have thoughts of self-harm or suicide at any time, contact your doctor or go to the hospital directly.
You may find it helpful to tell a relative or close 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 worried about changes in your behavior.
Dry mouth
Dry mouth has been reported in 10% of patients treated with venlafaxine. This may increase the risk of tooth decay (caries). Therefore, you should be careful with your dental hygiene.
Diabetes
Your blood glucose levels may be altered by Dobupal. Therefore, the doses of your diabetes medicines may need to be adjusted.
Dobupal should not normally be used in the treatment of children and adolescents under 18 years of age. Additionally, you should know that in patients under 18 years of age, there is a greater risk of side effects such as suicidal attempts, suicidal ideas, and hostility (mainly aggression, confrontational behavior, and irritation) when taking this class of medicines. Despite this, your doctor may prescribe this medicine to patients under 18 years of age when they decide what is best for the patient. If your doctor has prescribed this medicine to a patient under 18 years of age and you wish to discuss this decision, please go back to your doctor. You should inform your doctor if any of the above symptoms develop or worsen when these patients under 18 years of age are taking Dobupal. Additionally, long-term safety in relation to growth, maturity, and cognitive and behavioral development has not been established.
Tell your doctor or pharmacist if you are using or have recently used or might use any other medicines. Your doctor must decide if you can take Dobupal with other medicines.
Do not start or stop taking any medicines, including those that can be bought without a prescription, herbal remedies, and plant-based products, before checking with your doctor or pharmacist.
A potentially life-threatening condition, or reactions similar to Neuroleptic Malignant Syndrome (NMS) (see section “Possible side effects”) may occur with treatment with venlafaxine, particularly when taken with other medicines. 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). The signs and symptoms of NMS can include a combination of fever, rapid heartbeat, sweating, severe muscle stiffness, confusion, increased muscle enzymes (determined by a blood test).
Tell your doctor immediately or go to the emergency department of the nearest hospital if you think you are experiencing serotonin syndrome.
Tell your doctor if you are taking medicines that may affect your heart rhythm.
Some examples of these medicines include:
The following medicines may also interact with Dobupal and should be used with caution. It is especially important to mention to your doctor or pharmacist if you are taking medicines containing:
Dobupal should be taken with food (see section 3 “How to take Dobupal”)
Do not drink alcohol during treatment with Dobupal. Taking it with alcohol may cause extreme fatigue and unconsciousness, and worsen the symptoms of depression and other conditions, such as anxiety disorders.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. You should only take Dobupal after discussing with your doctor the possible benefits and risks to the unborn child.
If you take Dobupal in the final stages of pregnancy, there may be an increased risk of heavy vaginal bleeding shortly after delivery, especially if you have a history of bleeding disorders. Your doctor or midwife should know that you are taking Dobupal so they can advise you. When similar medicines (SSRIs) are taken during pregnancy, they may increase the risk of a serious condition in babies called persistent pulmonary hypertension of the newborn (PPHN), making the baby breathe faster and turn blue. These symptoms usually start during the first 24 hours after the baby is born. If this happens to your baby, you should contact your midwife and/or doctor immediately.
If you are taking this medicine during pregnancy, in addition to breathing problems, other symptoms your baby may have when born are feeding problems. If your baby has these symptoms when born and you are concerned, contact your doctor and/or midwife who can advise you.
Dobupal passes into breast milk. There is a risk of an effect on the baby. Therefore, you should discuss this with your doctor, and they will decide whether you should stop breastfeeding or stop taking this medicine.
Do not drive or use tools or machines until you know how this medicine affects you.
Important information about some of the ingredients of Dobupal
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, contact them before taking this medicine.
This medicine contains less than 23 mg of sodium (1mmol) per tablet; this is, essentially, “sodium-free”.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
The usual recommended initial dose is 75 mg per day in divided doses, two or three times a day. Your doctor may gradually increase the dose, and if necessary, even up to a maximum dose of 375 mg per day for depression.
Take Dobupal at approximately the same time each day, either in the morning or in the evening.
Dobupal 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 this medicine without talking to your doctor (see section “If you stop taking Dobupal”).
In case of overdose or accidental ingestion, contact your doctor, pharmacist, or call the Toxicology Information Service, phone 91 562 04 20, stating the medicine and the amount taken.
Overdose can put your life in danger, especially when taken with certain medicines and/or alcohol (see section “Taking Dobupal with other medicines”).
The symptoms of a possible overdose may include rapid heartbeat, 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 missed doses. Do not take more than the daily dose of Dobupal that has been prescribed for you in one day.
Do not stop taking your treatment or reduce the dose without your doctor's advice, even if you feel better. If your doctor thinks you no longer need Dobupal, they may ask you to reduce the dose gradually before stopping treatment completely. It is known that side effects occur when people stop using this medicine, especially when it is stopped suddenly or if the dose is reduced too quickly. Some patients may experience symptoms such as suicidal thoughts, aggression, fatigue, dizziness, instability, headache, insomnia, nightmares, dry mouth, loss of appetite, nausea, diarrhea, nervousness, agitation, confusion, ringing in the ears, tingling, or, in rare cases, sensations of electric shock, weakness, sweating, seizures, or symptoms similar to flu, vision problems, 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 Dobupal. This may take several weeks or months. In some patients, the discontinuation may need to be very gradual over months or more. If you experience any of these or other symptoms that bother you, consult your doctor for advice.
If you have any further questions on 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 Dobupal. Tell your doctor immediately, or go to the emergency room of 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). The signs and symptoms of NMS may include a combination of fever, rapid heartbeat, sweating, severe muscle stiffness, confusion, increased muscle enzymes (determined by a blood test).
Frequency not known (cannot be estimated from available data)
Other adverse effects that you should report to your doctorare (the frequency of these adverse effects is included in the list below "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)
Unexpected bleeding, for example, bleeding gums, blood in urine or vomit, or the appearance of unexpected bruises or broken blood vessels (broken veins).
Frequency not known (cannot be estimated from available data)
Dobupal 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, Dobupal may reduce the function of blood platelets, leading to an increased risk of bruising or bleeding. Therefore, your doctor may want to perform occasional blood tests, especially if you have been taking Dobupal for a long time.
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, 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, Website: 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 sight and reach of children.
Do not use this medicine after the expiration date shown on the packaging. The expiration date is the last day of the month indicated.
No special storage conditions are required. Store in a dry place.
Medicines should not be thrown down the drain or into the trash. Deposit the packaging and unused medicines in the SIGRE point of the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and unused medicines. This will help protect the environment.
The active ingredient is venlafaxine. Each tablet contains 84.84 mg of venlafaxine hydrochloride, equivalent to 75 mg of venlafaxine base.
The other components (excipients) are: lactose, microcrystalline cellulose, sodium starch glycolate, magnesium stearate, yellow iron oxide (E-172), and brown iron oxide (E-172).
Dobupal 75 mg is presented in the form of tablets. The tablets are circular, biplanar, with beveled edges, salmon-colored, and scored on one side.
Dobupal 75 mg is presented in packages containing 60 tablets for oral administration.
Marketing Authorization Holder
Almirall, S.A.
General Mitre, 151
08022 – Barcelona
Manufacturer
Industrias Farmacéuticas Almirall, S.A.
Ctra. de Martorell, 41-61
08740 Sant Andreu de la Barca – Barcelona (Spain)
This medicine was authorized in the EEA Member States with the following names:
Spain: Dobupal 75 mg tablets
Date of the last revision of this prospectus: May 2023
Detailed and updated information on 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 DOBUPAL 75 mg TABLETS in October, 2025 is around 19.15 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.