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ELONTRIL 150 mg MODIFIED-RELEASE TABLETS

ELONTRIL 150 mg MODIFIED-RELEASE TABLETS

Ask a doctor about a prescription for ELONTRIL 150 mg MODIFIED-RELEASE TABLETS

This page is for general information. Consult a doctor for personal advice. Call emergency services if symptoms are severe.
About the medicine

How to use ELONTRIL 150 mg MODIFIED-RELEASE TABLETS

Introduction

Package Leaflet:information for the user

Elontril 150 mg modified-release tablets

bupropion hydrochloride

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

  • Keep this leaflet, you may need to read it again.
  • If you have any further questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
  • If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

Contents of the pack

  1. What is Elontril and what is it used for
  2. What you need to know before you take Elontril
  3. How to take Elontril
  4. Possible side effects
  5. Storing Elontril
  6. Contents of the pack and other information

1. What is Elontril and what is it used for

Elontril is a medicine prescribed by your doctor for the treatment of depression. It is thought to work on certain substances in the brain called noradrenalineand dopamine.

2. What you need to know before you take Elontril

Do not take Elontril

  • to bupropion or any of the other ingredients of this medicine (listed in section 6)
  • (for example, bulimia or anorexia nervosa)
  • and have started, or are about to start, alcohol withdrawal
  • , or are going to stop taking them while taking Elontril
  • other medicines for depressioncalled monoamine oxidase inhibitors(MAOIs).

If you are in any of these situations, tell your doctor immediately and do not takeElontril.

Warnings and precautions

Talk to your doctor or pharmacist before you start taking Elontril.

Brugada syndrome

  • (a rare inherited condition that affects the heart rhythm) or if there has been a cardiac arrest or sudden death in your family.

Children and adolescents

Elontril is not recommended for the treatment of children under 18 years of age.

In patients under 18 years, there is an increased risk of suicidal thoughts and attempts when taking antidepressants.

Adults

Tell your doctor before you start takingElontril:

  • that is being treated with insulin or oral tablets

It has been observed that Elontril can cause epileptic seizures (convulsions) in approximately 1 in 1,000 people. This side effect is more likely to occur in people who are in the situations mentioned above. If you have a seizure while taking Elontril, stop taking Elontril. Do not take it again and see your doctor.

  • (severe mood swings), Elontril may cause episodes of this illness
  • the use of these medicines with Elontril may cause serotonin syndrome, a potentially life-threatening condition (see "Other medicines and Elontril" in this section)
  • , the likelihood of side effects is higher.

If you are in any of the situations mentioned above, talk to your doctor before taking Elontril, who may decide to monitor you more closely or recommend another treatment.

Suicidal thoughts and worsening of your depression

If you are depressed, you may sometimes have thoughts of harming or killing yourself. These thoughts may increase at the start of treatment with antidepressants, as all these medicines take time to work, usually about two weeks, but sometimes longer.

This is more likely to happen:

  • . There is information from clinical trials that shows an increased risk of suicidal behavior in young adults under 25 years of age with psychiatric disorders who are being treated with an antidepressant.

If you have thoughts of killing or harming yourself at any time, talk to your doctor or go to the hospital immediately.

It may be helpful for you to tell a relative or close friendthat 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.

Other medicines and Elontril

Stop taking Elontril and tell your doctor if you are taking or have taken in the last two weeksantidepressant medicines calledmonoamine oxidase inhibitors(MAOIs) (see also section 2 "Do not take Elontril").

Tell your doctor or pharmacist that you are taking, have recently taken, or might take any other medicines, vitamins, or herbal products, including those bought without a prescription. Your doctor may change your dose of Elontril or recommend a change in the other medicines.

Some medicines interact with Elontril. Some of them may increase the likelihood of having seizures or convulsions, and others may increase the risk of having other side effects. The following are some examples, although the list is not complete.

May increase the possibility of having seizures

  • , used to treat asthma or other lung diseases
  • , a strong pain reliever
  • , or if you are going to stop taking them while taking Elontril (see also section 2 "Do not take Elontril")
  • (such as mefloquine or chloroquine)
  • .

If you are in any of these situations, tell your doctor immediately before taking Elontril. Your doctor will assess the risks and benefits of taking Elontril.

May increase the possibility of having other side effects

  • (amitriptyline, fluoxetine, paroxetine, citalopram, escitalopram, venlafaxine, dosulepin, desipramine, or imipramine) or other mental illnesses (clozapine, risperidone, thioridazine, or olanzapine). Elontril may interact with some medicines used to treat depression and may experience changes in mental status (such as agitation, hallucinations, coma) and other side effects such as body temperature above 38°C, increased heart rate, unstable blood pressure, exaggerated reflexes, muscle stiffness, lack of coordination, and/or gastrointestinal symptoms (such as nausea, vomiting, diarrhea)
  • (levodopa, amantadine, or orphenadrine)
  • Elontril(carbamazepine, phenytoin, valproate)
  • (such as cyclophosphamide or ifosfamide)
  • (metoprolol)
  • (propafenone, flecainide)
  • .

If you are in any of these situations, tell your doctor immediately before taking Elontril.

Elontril may be less effective

  • or efavirenz, medicines for treating HIV (AIDS) infection.

Tell your doctor if you are taking any of these medicines. Your doctor will check if Elontril is working properly in you. You may need to increase the dose or change to another treatment for your depression. Do not increasethe dose of Elontril unless your doctor advises you to, as this may increase the risk of having side effects, including seizures.

Elontril may make other medicines less effective

  • .

Tell your doctor if you are in this situation. You may need to change your treatment for depression.

  • .

Tell your doctor if you are in this situation. Your doctor may consider adjusting the dose of digoxin.

Using Elontril and alcohol

Alcohol may affect how Elontril works and, when taken together, may rarely affect your nerves or mental state. Some people have noticed that they are more sensitive to alcohol during treatment with Elontril. Your doctor may recommend that you do not drink alcohol (beer, wine, spirits) or that you drink very small amounts while taking Elontril. If you currently drink a lot of alcohol, do not stop suddenly, as you may be at risk of having a seizure.

Ask your doctor about drinking alcoholbefore starting treatment with Elontril.

Effect on urine tests

Elontril may interfere with some urine tests used to detect other medicines or substances. If you need a urine test, tell your doctor or hospital that you are taking Elontril.

Pregnancy and breastfeeding

Do not take Elontril if you are pregnant, think you may be pregnant, or are planning to become pregnant unless your doctor has prescribed it for you. Talk to your doctor or pharmacist before using this medicine. Some studies, but not all, have reported an increased risk of birth defects, particularly heart defects, in babies whose mothers were taking Elontril. It is not known if this is due to the use of Elontril.

The components of Elontril may pass into breast milk. Talk to your doctor or pharmacist before taking Elontril.

Driving and using machines

Do not drive or use tools or machines if Elontril makes you feel dizzy or drowsy.

3. How to take Elontril

Follow exactly the administration instructions of this medicine given by your doctor or pharmacist. The recommended doses are included below, but your doctor will advise you on the dose that is right for you. If you are unsure, talk to your doctor or pharmacist again.

It may take some time before you start to feel better. The medicine takes time to work fully, which can be weeks or months. When you start to feel better, your doctor may advise you to continue taking Elontril to prevent your depression from coming back.

What dose to take

The usual recommended dose in adults is one150 mg tablet per day.

If after several weeks you do not start to feel better, your doctor may increase the dose to 300 mg per day.

Take the Elontril tablets in the morning. Do not take Elontril more than once a day.

The tablet is covered by a film that slowly releases the medicine in your body. Sometimes you may notice that a kind of tablet appears in your stool. This is the empty film coating that has passed through your intestine.

Prohibition sign with a large purple cross on a white background indicating do not use or avoidSwallow the tablets whole. Do not chew, crush, or divide them, as this can lead to an overdose due to the rapid release of the medicine in your body, increasing the likelihood of side effects, including seizures.

Some people may maintain a dose of one 150 mg tablet per daythroughout treatment. Your doctor may prescribe this dose in patients with liver or kidney problems.

Duration of treatment

Talk to your doctor, who will indicate the duration of treatment withElontril. It may take several weeks or months before you notice any improvement. Keep your doctor informed about your symptoms so that they can decide on the duration of treatment. Although you may start to feel better, your doctor may recommend continuing treatment with Elontril to prevent the symptoms of depression from coming back.

If you take more Elontril than you should

In case of overdose or accidental ingestion, talk to your doctor or pharmacist immediately, or go to the emergency department or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medicine and the amount taken.

If you take more tablets than your doctor prescribed, you may increase the risk of having seizures or convulsions.

If you forget to take Elontril

If you miss a dose, wait and take the next dose at the usual time.

Do not take a double dose to make up forforgotten doses.

If you stop taking Elontril

Do not stop taking Elontril or reduce the dose without talking to your doctor first.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. Possible Adverse Effects

Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.

Severe Adverse Effects

Epileptic Seizures or Convulsions

Approximately 1 in every 1,000 people taking Elontril are at risk of suffering an epileptic seizure (a seizure or convulsion). This risk is higher if you take more tablets than you should, if you are taking certain medications, or if you have a higher than usual risk of suffering seizures. If you have any doubts, ask your doctor.

  • Consult your doctor if you suffer an epileptic seizureand do not take any more tablets.

Allergic Reactions

Some people may have allergic reactions to Elontril, including:

  • Redness or skin rash (urticaria), blisters, or hives on the skin. Some skin rashes may require hospitalization, especially if they are accompanied by swelling of the mouth and eyes.
  • Abnormal appearance of "wheezing" in the chest or difficulty breathing.
  • Swelling of eyelids, lips, or tongue.
  • Pain in muscles or joints.
  • Fainting or loss of consciousness.
  • Consult your doctor if you suffer an allergic reactionand do not take any more tablets.

Allergic reactions can last for a long time.If your doctor prescribes any medication for this, make sure to complete the treatment.

Cutaneous Lupus Erythematosus or Worsening of Lupus Symptoms

Unknown frequency: the frequency cannot be estimated with the available data from people taking Elontril. Lupus is a disorder of the immune system that affects the skin and other organs.

  • If you experience aworsening of lupus, skin rash, or lesions (particularly in sun-exposed areas) while taking Elontril, contact your doctor immediately, as it may be necessary to interrupt treatment.

Acute Generalized Exanthematous Pustulosis (AGEP)

Unknown frequency: the frequency cannot be estimated with the available data from people taking Elontril.

The symptoms of AGEP include a rash with pus-filled blisters/grains.

  • If you experience a rash with pus-filled blisters/grains, contact your doctor immediately, as it may be necessary to interrupt treatment.

Other Adverse Effects

Very Common Adverse Effects

These may affect more than 1 in every 10 people:

  • Difficulty sleeping. Make sure to take Elontril in the morning.
  • Headache
  • Dry mouth
  • Nausea, vomiting.

Common Adverse Effects

These may affect up to 1 in every 10 people:

  • Fever, dizziness, itching, sweating, and skin rash (sometimes due to allergic reactions)
  • Instability, tremors, weakness, fatigue, chest pain
  • Feeling anxious or agitated
  • Stomach pain or digestive discomfort (constipation), alterations in taste, loss of appetite (anorexia)
  • Increased blood pressure (sometimes severe), flushing
  • Feeling of ringing in the ears, vision disturbances.

Uncommon Adverse Effects

These may affect up to 1 in every 100 people:

  • Feeling depressed (see also section 2 "Special warnings and precautions for use", in "Suicidal thoughts and worsening of depression")
  • Confusion
  • Difficulty concentrating
  • Accelerated heart rate
  • Weight loss.

Rare Adverse Effects

These may affect up to 1 in every 1,000 people:

  • Seizures.

Very Rare Adverse Effects

These may affect up to 1 in every 10,000 people:

  • Palpitations, fainting
  • Muscle spasms, muscle stiffness, lack of coordination, walking difficulties, or coordination problems
  • Feeling of restlessness, irritability, hostility, aggression, nightmares, tingling, or numbness, memory loss
  • Yellowing of the skin or whites of the eyes (jaundice) that may be associated with an increase in liver enzymes, hepatitis
  • Severe allergic reactions; skin rash accompanied by joint and muscle pain
  • Changes in blood sugar levels
  • Increased or decreased frequency of urination
  • Urinary incontinence (involuntary urination, loss of urine)
  • Severe skin rashes that can affect the mouth or other parts of the body and can be life-threatening
  • Worsening of psoriasis (thickened or reddened skin plaques)
  • Loss or unusual thinning of hair (alopecia)
  • Feelings of unreality or strangeness (depersonalization); seeing or hearing things that do not exist (hallucinations); feeling or believing unrealistic things (delusional ideas); severe distrust (paranoia).

Unknown Frequency

Other adverse effects have occurred in a small number of people, but their exact frequency is unknown:

  • Thoughts of self-harm or suicide during treatment with Elontril or shortly after stopping treatment (see section 2, "What you need to know before taking Elontril"). If you have these thoughts, contact your doctor or go to the hospital immediately
  • Loss of contact with reality and inability to think or judge clearly (psychosis); other symptoms may include hallucinations and/or illusions
  • Sudden feeling of intense fear (panic attack)
  • Stuttering
  • Decreased number of red blood cells (anemia), white blood cells (leukopenia), and platelets (thrombocytopenia)
  • Decreased sodium levels in the blood (hyponatremia)
  • Changes in mental state (e.g., agitation, hallucinations, coma) and other adverse effects such as body temperature above 38°C, increased heart rate, unstable blood pressure, exaggerated reflexes, muscle stiffness, lack of coordination, and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea) while taking Elontril with other medications used to treat depression (such as paroxetine, citalopram, escitalopram, fluoxetine, and venlafaxine).

Reporting Adverse Effects

If you experience any adverse effects, consult your doctor or pharmacist, even if they are possible adverse effects that are not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.

5. Storage of Elontril

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiration date stated on the packaging. The expiration date is the last day of the month indicated.

Store in the original packaging to protect it from moisture and light. The bottle contains a small sealed container containing activated carbon and silica gel to keep the tablets dry. Keep the container inside the bottle. Do not swallow.

Medicines should not be disposed of via wastewater or household waste. Deposit the packaging and any unused medicines in the pharmacy's SIGRE point. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.

6. Package Contents and Additional Information

Composition ofElontril

The active ingredient is bupropion hydrochloride. Each tablet contains 150 mg of bupropion hydrochloride.

The other ingredients are:

Core of the tablet:Poly(vinyl alcohol), dibehenate of glycerol.

Coating:Ethylcellulose, povidone K-90, macrogol 1450, dispersion of methacrylic acid and ethyl acrylate copolymer, silicon dioxide, triethyl citrate.

Printing ink:Shellac Glaze, iron oxide black (E172), and ammonium hydroxide.

Appearance of the Product and Package Contents

Elontril 150 mg tablets are white-cream to light yellow, round tablets, with one face marked with "GS 5FV 150" in black ink and the other smooth. They are available in white polyethylene bottles containing 7, 30, 90, or 90 (3 x 30) tablets.

Not all pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder

GlaxoSmithKline, S.A.

P.T.M. C/ Severo Ochoa, 2

28760 Tres Cantos (Madrid)

Tel: +34 900 202 700

[email protected]

Manufacturer

Glaxo Wellcome S.A.

Avenida de Extremadura, 3

09400 Aranda de Duero, Burgos

Spain

This medicine is authorized in the Member States of the European Economic Area under the following names:

Wellbutrin XR: Austria, Belgium, Cyprus, Greece, Luxembourg, Malta, Poland, Portugal, Slovenia, Netherlands.

Wellbutrin: Italy.

Elontril: Czech Republic, Estonia, Germany, Hungary, Italy, Lithuania, Portugal, Romania, Slovakia, Spain, Netherlands.

Wellbutrin Retard: Iceland, Norway.

Voxra: Finland, Sweden.

Date of the last revision of thisleaflet:March 2024

Detailed and up-to-date information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/

About the medicine

How much does ELONTRIL 150 mg MODIFIED-RELEASE TABLETS cost in Spain ( 2025)?

The average price of ELONTRIL 150 mg MODIFIED-RELEASE TABLETS in November, 2025 is around 13 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.

Alternatives to ELONTRIL 150 mg MODIFIED-RELEASE TABLETS in other countries

The best alternatives with the same active ingredient and therapeutic effect.

Alternative to ELONTRIL 150 mg MODIFIED-RELEASE TABLETS in Poland

Dosage form: Tablets, 150 mg
Active substance: bupropion
Marketing authorisation holder (MAH): neuraxpharm Arzneimittel GmbH
Prescription required
Dosage form: Tablets, 150 mg
Active substance: bupropion
Marketing authorisation holder (MAH): neuraxpharm Arzneimittel GmbH
Prescription required
Dosage form: Tablets, 300 mg
Active substance: bupropion
Marketing authorisation holder (MAH): neuraxpharm Arzneimittel GmbH
Prescription required
Dosage form: Tablets, 150 mg
Active substance: bupropion
Marketing authorisation holder (MAH): Neuraxpharm Bohemia s.r.o.
Prescription required
Dosage form: Tablets, 300 mg
Active substance: bupropion
Marketing authorisation holder (MAH): GlaxoSmithKline, S.A.
Prescription required
Dosage form: Tablets, 150 mg
Active substance: bupropion
Marketing authorisation holder (MAH): GlaxoSmithKline, S.A.
Prescription required

Alternative to ELONTRIL 150 mg MODIFIED-RELEASE TABLETS in Ukraine

Dosage form: tablets, modified-release tablets, 150mg
Active substance: bupropion
Manufacturer: BALKANFARMA-DUPNICA AD
Prescription required
Dosage form: tablets, 60 mg
Prescription not required

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