ESCITALOPRAM VISO FARMACEUTICA 10 mg FILM-COATED TABLETS

2. What you need to know before taking Escitalopram Viso Farmacéutica

Do not take Escitalopram Viso Farmacéutica

• If you are allergic to escitalopram or any of the other ingredients of this medication (listed in section 6).

• If you are taking any other medication that belongs to a group called monoamine oxidase inhibitors (MAOIs), such as selegiline (used to treat Parkinson's disease), moclobemide (used to treat depression), and linezolid (an antibiotic).
• If you were born with or have had an episode of abnormal heart rhythm (observed on an ECG; an examination to evaluate heart function).
• If you are taking medications for heart rhythm problems or that may affect it (see section 2 "Other medications and Escitalopram Viso Farmacéutica").

Warnings and Precautions

Consult your doctor or pharmacist before starting to take Escitalopram Viso Farmacéutica.

Tell your doctor if you have any other disorder or disease, as your doctor may need to take it into account. Especially tell your doctor:

• If you have epilepsy. Treatment with Escitalopram Viso Farmacéutica will be discontinued if you have seizures for the first time or if there is an increase in the frequency of these (see also section 4 "Possible side effects").
• If you have liver or kidney failure. Your doctor may need to adjust your dose.
• If you have diabetes, treatment with Escitalopram Viso Farmacéutica may alter blood sugar control (blood sugar levels). It may be necessary to adjust the dosage of insulin or oral hypoglycemic medication.
• If you have low sodium levels in the blood.
• If you are prone to developing bleeding or bruising easily.
• If you are receiving electroconvulsive therapy (shock treatment).
• If you have coronary heart disease.
• If you have or have had heart problems or have recently had a heart attack.
• If you have a low resting heart rate and/or know that you may have a decrease in salt levels due to severe and prolonged diarrhea and vomiting (due to illness) or due to the use of diuretics (pills to urinate).
• If you experience rapid or irregular heartbeats, fainting, collapse, or dizziness when standing up, which could indicate abnormal heart rhythm.
• If you have or have had eye problems, such as certain types of glaucoma (increased pressure in the eye).
• If you have a history of bleeding disorders or if you are pregnant (see Pregnancy, Breastfeeding, and Fertility).

Please note that:

Some patients with manic-depressive illness may enter a manic phase. This is characterized by strange and rapidly changing ideas, inappropriate happiness, and excessive physical activity. If you experience this, contact your doctor.

Symptoms such as restlessness or difficulty sitting or standing may also occur during the first few weeks of treatment. Tell your doctor immediately if you experience these symptoms.

Some medications in the same group as Escitalopram Viso Farmacéutica (called SSRIs/SNRIs) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms persist after treatment is discontinued.

Suicidal thoughts or worsening of your depression or anxiety disorder

If you are depressed or have anxiety disorders, you may occasionally have thoughts of harming yourself or committing suicide. This may increase when you start taking antidepressants, as these medications take time to work, usually a couple of weeks, but sometimes more. You are more likely to think this way:

• If you had previously had thoughts of committing suicide or self-harm.
• If you are a young adult. Clinical trial information has shown an increased risk of suicidal behavior in young adults under 25 years of age with psychiatric disorders who received antidepressant treatment.

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

It may be helpful to tell a relative or close friendthat you are depressed or have an anxiety disorder and ask them to read this package leaflet. You could ask them to tell you if they think your depression or anxiety is getting worse or if they are concerned about changes in your behavior.

Use in children and adolescents

Escitalopram Viso Farmacéutica is not normally used in children and adolescents under 18 years of age. Additionally, you should know that patients under 18 are at a higher risk of side effects, such as suicidal attempts, suicidal thoughts, and hostility (mainly aggression, oppositional behavior, and anger) when taking this class of medications. Nevertheless, your doctor may prescribe Escitalopram Viso Farmacéutica to patients under 18 if they decide it is best for them. If your doctor has prescribed Escitalopram Viso Farmacéutica to a patient under 18 and you want to discuss it, talk to them again. Tell your doctor if any of these symptoms appear or worsen in patients under 18 taking Escitalopram Viso Farmacéutica. Additionally, the long-term safety effects of Escitalopram Viso Farmacéutica regarding growth, maturation, and cognitive and behavioral development in this age group have not yet been demonstrated.

Other medications and Escitalopram Viso Farmacéutica

Use of Escitalopram Viso Farmacéutica with other medications. Tell your doctor or pharmacist if you are using, have recently used, or may need to take any other medication.

Tell your doctor if you are taking any of the following medications:

• Non-selective monoamine oxidase inhibitors (MAOIs) that contain phenelzine, iproniazid, isocarboxazid, nialamide, and tranylcypromine as active ingredients. If you have taken any of these medications, you will need to wait 14 days before starting to take Escitalopram Viso Farmacéutica. When you stop taking Escitalopram Viso Farmacéutica, you should wait 7 days before taking any of these medications.

• Reversible inhibitors of monoamine oxidase A (RIMAs) that contain moclobemide (used to treat depression).
• Irreversible inhibitors of monoamine oxidase B (MAO-B) that contain selegiline (used to treat Parkinson's disease). These increase the risk of side effects.
• The antibiotic linezolid.
• Lithium (used to treat manic-depressive disorder) and tryptophan.
• Imipramine and desipramine (both used to treat depression).
• Sumatriptan and similar medications (used to treat migraines) and tramadol (used to treat severe pain). These increase the risk of side effects.
• Opioids such as buprenorphine. These medications may interact with Escitalopram Viso Farmacéutica and may cause symptoms such as involuntary and rhythmic muscle contractions, including muscles that control eye movements, agitation, hallucinations, coma, excessive sweating, tremors, exaggerated reflexes, increased muscle tension, and body temperature above 38°C. Contact your doctor if you experience these symptoms.
• Cimetidine, lansoprazole, and omeprazole (used to treat stomach ulcers), fluconazole (used to treat fungal infections), fluvoxamine (antidepressant), and ticlopidine (used to reduce the risk of stroke). These may cause an increase in blood levels.
• St. John's Wort (Hypericum perforatum) – a medicinal plant used for depression.
• Acetylsalicylic acid (aspirin) and non-steroidal anti-inflammatory drugs (medications used for pain relief or to thin the blood, known as anticoagulants). This may increase the tendency to bleed.
• Warfarin, dipyridamole, and fenprocoumon (medications used to thin the blood, known as anticoagulants).

Your doctor will likely check your blood coagulation time when starting and stopping Escitalopram to verify that the anticoagulant dose is adequate.

• Mefloquine (used to treat malaria), bupropion (used to treat depression), and tramadol (used to treat intense pain) due to the possible risk of reducing the seizure threshold.
• Neuroleptics (medications for treating schizophrenia, psychosis) and antidepressants (tricyclic antidepressants and SSRIs) due to a possible risk of reducing the seizure threshold.
• Flecainide, propafenone, and metoprolol (used in cardiovascular diseases), clomipramine and nortriptyline (antidepressants), and risperidone, thioridazine, and haloperidol (antipsychotics). It may be necessary to adjust the dosage of Escitalopram Viso Farmacéutica.
• Medications that decrease potassium or magnesium levels in the blood, as this increases the risk of heart rhythm disorders, which pose a risk to life.

DO NOT TAKE Escitalopram Viso Farmacéuticaif you are taking medications for heart rhythm problems or medications that may affect it, such as antiarrhythmics of classes IA and III, antipsychotics (e.g., phenothiazine derivatives, pimozide, haloperidol), tricyclic antidepressants, certain antimicrobials (e.g., sparfloxacin, moxifloxacin, erythromycin IV, pentamidine, halofantrine, particularly in antimalarial treatment), certain antihistamines (e.g., astemizole, hydroxyzine, mizolastine). If you have any further questions, consult your doctor.

Taking Escitalopram Viso Farmacéutica with food, drinks, and alcohol.

Escitalopram Viso Farmacéutica can be taken with or without food (see section 3 "How to take Escitalopram Viso Farmacéutica").

As with many medications, it is not recommended to combine Escitalopram Viso Farmacéutica with alcohol, although it is not expected that Escitalopram Viso Farmacéutica will interact with alcohol.

Pregnancy, Breastfeeding, and Fertility

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication. Do not take Escitalopram Viso Farmacéutica if you are pregnant or breastfeeding, unless you and your doctor have discussed the relevant risks and benefits.

If you take Escitalopram Viso Farmacéutica during the last 3 months of pregnancy, you should know that the following effects may be observed in your newborn: respiratory difficulties, blue skin color, seizures, changes in body temperature, feeding difficulties, vomiting, low blood sugar, stiff or soft muscles, intense reflexes, tremors, nervousness, irritability, lethargy, constant crying, and sleep disturbances. If your newborn has any of these symptoms, contact your doctor immediately.

Make sure the midwife or your doctor knows that you are taking Escitalopram Viso Farmacéutica. When taken during pregnancy, especially in the last 3 months, medications like Escitalopram Viso Farmacéutica may increase the risk of a serious disorder in children called persistent pulmonary hypertension of the newborn (PPHN), which causes the baby to breathe faster and turn blue. These symptoms usually start within the first 24 hours after the baby's birth. If this happens to your child, contact your midwife or doctor immediately.

If you take Escitalopram Viso Farmacéutica 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 Escitalopram Viso Farmacéutica to advise you accordingly.

If Escitalopram Viso Farmacéutica is used during pregnancy, it should never be stopped abruptly.

Escitalopram/metabolites are excreted in breast milk.

It has been observed that citalopram, a medication similar to escitalopram, reduces sperm quality in animal studies. In theory, this could affect fertility, but to date, no impact on human fertility has been observed.

Driving and Using Machines

You are advised not to drive or use machines until you know how Escitalopram Viso Farmacéutica affects you.

Escitalopram Viso Farmacéutica contains sodium

This medication contains less than 1 mmol of sodium (23 mg) per tablet; it is essentially "sodium-free".

3. How to Take Escitalopram Viso Farmacéutica

Follow the administration instructions for this medication exactly as indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.

Adults

Depression

The recommended dose is 10 mg taken once a day. Your doctor may increase the dose up to a maximum of 20 mg per day.

Panic Disorder

The initial dose is 5 mg in a single daily dose for the first week, before increasing the dose to 10 mg per day. Your doctor may increase the dose further up to a maximum of 20 mg per day.

Social Anxiety Disorder

The recommended dose is 10 mg taken once a day. Your doctor may reduce the dose to 5 mg per day or increase the dose up to a maximum of 20 mg per day, depending on how you respond to the medication.

Generalized Anxiety Disorder

The recommended dose is 10 mg taken once a day. Your doctor may increase the dose up to a maximum of 20 mg per day.

Obsessive-Compulsive Disorder

The recommended dose is 10 mg taken once a day. Your doctor may increase the dose up to a maximum of 20 mg per day.

Elderly Patients (over 65 years):

The initial dose is 5 mg, taken in a single daily dose. The doctor may increase the dose to 10 mg per day.

Use in Children and Adolescents

Escitalopram Viso Farmacéutica is not normally administered to children or adolescents. For more information, consult section 2 "Warnings and Precautions".

Renal Insufficiency

Caution is advised in patients with severely decreased renal function. Take it as prescribed by your doctor.

Hepatic Insufficiency

Patients with liver problems should not receive more than 10 mg per day. Take it as prescribed by your doctor.

Patients Considered as Slow Metabolizers of CYP2C19

Patients with this known genotype should not receive more than 10 mg per day. Take it as prescribed by your doctor.

How to Take Escitalopram Viso Farmacéutica

You can take Escitalopram Viso Farmacéutica with or without food. Swallow the tablet with a little water. Do not chew it, as it has a bitter taste.

If necessary, you can divide the tablets by placing the tablet on a flat surface, with the score line facing up. The tablets can be broken by pressing on each end of the tablet, using both index fingers.

Duration of Treatment

It may take a couple of weeks to start feeling better. Continue taking Escitalopram Viso Farmacéutica even if it takes some time before you notice an improvement in your condition.

Do not change the dose of your medication without discussing it with your doctor first.

Continue taking Escitalopram Viso Farmacéutica for the time advised by your doctor.

If you stop treatment too early, your symptoms may reappear. It is recommended to continue treatment for at least 6 months after you feel better.

If You Take More Escitalopram Viso Farmacéutica Than You Should

If you take more doses of Escitalopram Viso Farmacéutica than prescribed, contact your doctor or the nearest emergency service immediately. Do this even if you do not feel any discomfort. Some signs of overdose could be dizziness, tremors, agitation, convulsion, coma, nausea, vomiting, changes in heart rhythm, reduction of blood pressure, and changes in fluid/salt balance in the body. Bring the box/packaging of Escitalopram Viso Farmacéutica with you when you go to the doctor or hospital.

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.

If You Forget to Take Escitalopram Viso Farmacéutica

Do not take a double dose to make up for missed doses. If you forget to take a dose and remember before bedtime, take it immediately. Continue as usual the next day. If you remember in the evening or the next day, skip the missed dose and continue as usual.

If You Interrupt Treatment with Escitalopram Viso Farmacéutica

Do not stop taking Escitalopram Viso Farmacéutica until your doctor tells you to do so. When you have finished your treatment cycle, it is generally recommended to gradually reduce the dose of Escitalopram Viso Farmacéutica.

When you stop taking Escitalopram Viso Farmacéutica, especially if it is sudden, you may notice withdrawal symptoms. These are common when treatment with Escitalopram Viso Farmacéutica is discontinued. The risk is greater when Escitalopram Viso Farmacéutica has been used for a long time or at high doses or when the dose is reduced too quickly. Most people notice that the symptoms are mild and disappear on their own within a couple of weeks. However, in some patients, they can be severe or prolonged (2-3 months or more). If you suffer from severe withdrawal symptoms when you stop taking Escitalopram Viso Farmacéutica, contact your doctor. They may ask you to start taking the tablets again and withdraw them more slowly.

Withdrawal symptoms include: Dizziness (instability or imbalance), feeling of muscle aches, feeling of burning, and (less frequently) feeling of electric shock (including the head), sleep disorders (vivid dreams, nightmares, inability to stay asleep), feeling of anxiety, headache, nausea (dizziness), sweating (with night sweats), restlessness or agitation, tremors (shivering), feeling of confusion or disorientation, feeling sensitive or irritable, diarrhea (loose stools), visual disturbances, fluttering or strong heartbeats (palpitations).

If you have any other doubts about the use of this medication, ask your doctor or pharmacist.

4. Possible Adverse Effects

Like all medications, this medication can cause adverse effects, although not all people experience them.

Adverse effects usually disappear after a few weeks of treatment. Note that many effects can also be symptoms of your illness and, therefore, will improve as you start to feel better.

If you experience any of the following symptoms, you should contact your doctor or go to the hospital immediately:

Uncommon (may affect 1 in 100 people):

• Unusual bleeding, such as gastrointestinal bleeding

Rare (may affect 1 in 1,000 people):

• Inflammation of the skin, tongue, lips, pharynx, or face, hives, or difficulty breathing or swallowing (severe allergic reaction), contact your doctor or go to the hospital immediately.
• High fever, agitation, confusion, tremors, and sudden muscle contractions can be signs of a rare disorder called serotonin syndrome. If you experience this, contact your doctor.

Unknown frequency (frequency cannot be estimated from available data):

• Difficulty urinating
• Seizures (attacks), see also the "Warnings and Precautions" section.
• Yellowing of the skin and whites of the eyes are signs of liver function alteration/hepatitis
• Fast or irregular heartbeats, fainting, which could be symptoms of a life-threatening disorder known as Torsades de Pointes
• Thoughts of self-harm or thoughts of suicide (cases of suicidal ideas and behaviors), see also "Warnings and Precautions" section
• Sudden inflammation of the skin mucosa (angioedema)
• Abundant vaginal bleeding shortly after childbirth (postpartum hemorrhage), see "Pregnancy" in section 2 for more information.

In addition to these, the following side effects have been reported

Very common (may affect more than 1 in 10 people):

• Feeling of dizziness (nausea)
• Headache

Common (may affect 1 in 10 people):

• Nasal congestion (sinusitis)
• Increased or decreased appetite
• Anxiety, restlessness, abnormal dreams, difficulty staying asleep, somnolence, dizziness, yawning, tremors, skin itching.
• Diarrhea, constipation, vomiting, dry mouth
• Increased sweating.
• Pain in muscles and joints (arthralgia and myalgia)
• Sexual disorders (delayed ejaculation, erection problems, reduced sexual desire, and women may have difficulty achieving orgasm).
• Fatigue, fever
• Weight gain

Uncommon (may affect 1 in 100 people):

• Hives, eczema, itching (pruritus)
• Teeth grinding, agitation, nervousness, panic attack, state of confusion
• Sleep disorder, taste perversion, fainting (syncope)
• Pupil dilation (mydriasis), visual disturbance, ringing in the ears (tinnitus)
• Hair loss
• Excessive menstrual bleeding
• Irregular menstrual period
• Weight loss
• Fast heartbeats
• Inflammation of the arms or legs
• Nosebleeds

Rare (may affect 1 in 1,000 people):

• Aggression, depersonalization, hallucinations
• Slow heartbeat

Unknown frequency (frequency cannot be estimated from available data):

• Cases of suicidal ideas and behaviors, see also "Warnings and Precautions" section
• Decrease in sodium levels in the blood (symptoms are dizziness and malaise with muscle weakness or confusion)
• Dizziness when standing up due to low blood pressure (orthostatic hypotension)
• Alterations in liver function tests (increase in liver enzyme levels in the blood)
• Movement disorders (involuntary muscle movements).
• Painful erections (priapism)
• Signs of abnormal bleeding, for example, from the skin or mucous membranes (ecchymosis).
• Increased secretion of a hormone called ADH, causing the body to retain water and dilute the blood, reducing sodium levels (inappropriate ADH secretion)
• Milk flow in women who are not breastfeeding
• Mania
• An increased risk of bone fractures has been observed in patients treated with this type of medication.
• Alteration of heart rhythm (called "prolongation of the QT interval", observed in the ECG, heart electrical activity).

In addition, it is known that a series of side effects occur with drugs that work similarly to Escitalopram Viso Farmacéutica. These are:

• Motor restlessness (akathisia)
• Lack of appetite

Reporting of Adverse Effects

If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that does not appear in this prospectus. You can also report them directly through the national reporting system: Spanish Medication Pharmacovigilance System Website: www.notificaRAM.es.

By reporting adverse effects, you can contribute to providing more information on the safety of this medication.

5. Conservation of Escitalopram Viso Farmacéutica

Keep this medication out of sight and reach of children.

Do not use this medication after the expiration date that appears on the blister pack and the box after "CAD". The expiration date is the last day of the month indicated.

This medication does not require special storage conditions.

Medications should not be thrown away through the sewers or in the trash. Deposit the packaging and medications you no longer need in the SIGRE Point of the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This way, you will help protect the environment.

6. Package Contents and Additional Information

Composition of Escitalopram Viso Farmacéutica

The active ingredient is escitalopram. Each Escitalopram Viso Farmacéutica tablet contains 10 mg of escitalopram (in the form of oxalate).

The other components are:

Core of the tablet:

Microcrystalline cellulose (E460), sodium croscarmellose (E468), magnesium stearate (E572), anhydrous colloidal silica, and talc

Coating of the tablets:

Hypromellose (E464), titanium dioxide (E171), Macrogol 400.

Appearance of the Product and Package Contents

Escitalopram Viso Farmacéutica is presented in 10 mg film-coated tablets. They are described below:

Film-coated tablets are white to off-white, oval, biconvex, with 'E 2' engraved on one face and scored on the other face. The tablet can be divided into two equal halves.

The tablets are packaged in smooth aluminum/aluminum blisters or PVC-Aclar/aluminum blisters.

Escitalopram Viso Farmacéutica is available in the following package sizes:

Blisters: 14, 20, 28, 50, 56, 100, and 200 tablets

It is possible that only some package sizes are marketed.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder:

Glenmark Arzneimittel GmbH

Industriestr. 31

82194 Gröbenzell

Germany

Manufacturer:

Glenmark Pharmaceuticals s.r.o.

Fibichova 143

566 17 Vysoké Mýto

Czech Republic

You can request more information about this medication by contacting the local representative of the Marketing Authorization Holder:

Glenmark Farmacéutica, S.L.U.

C/ Retama 7, 7th floor

28045 Madrid

Spain

This medication is authorized in the Member States of the European Economic Area with the following names:

Germany: Escitalopram Glenmark 10 mg Filmtabletten

Austria: Escitalopram Tillomed 10 mg Filmtabletten

Spain: Escitalopram Viso Farmacéutica 10 mg film-coated tablets EFG

Ireland: Escitalopram Glenmark 10 mg Film-coated tablets

Sweden: Escitalopram Glenmark 10 mg film-coated tablets

Date of the Last Revision of this Prospectus:June 2021.

Detailed information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/