Escitalopram 15 mg Orodispersible Tablets – patient leaflet, side effects, dosage

What Escitalopram is and what it is used for

Escitalopram 10 mg, 15 mg and 20 mg Orodispersible Tablets contains the active substance Escitalopram. Escitalopram belongs to a group of antidepressants called selective serotonin reuptake inhibitors (SSRIs).

Escitalopram is used to treat depression (major depressive episodes) and anxiety disorders (such as panic disorder with or without agoraphobia, social anxiety disorder, generalised anxiety disorder and obsessive-compulsive disorder).

It may take a couple of weeks before you start to feel better. Continue to take Escitalopram, even if it takes some time before you feel any improvement in your condition.

You must talk to a doctor if you do not feel better or if you feel worse.

2.

What you need to know before you use Escitalopram

Do not take Escitalopram if:

• if you are allergic to Escitalopram or any of the other ingredients of this medicine

  • (listed in section 6).

• If you take other medicines which belong to a group called MAO inhibitors,

  • including selegiline (used in the treatment of Parkinson’s disease), moclobemide (used in the treatment of depression) and linezolid (an antibiotic).

• If you are born with or have had an episode of abnormal heart rhythm (seen at

  • ECG; an examination to evaluate how the heart is functioning).

• If you take medicines for heart rhythm problems or that may affect the heart’s

  • rhythm (see section 2 “other medicines and Escitalopram”).

Warnings and precautions

Tell your doctor or pharmacist before taking Escitalopram. Please tell your doctor if you have any other condition or illness, as your doctor may need to take this into consideration. In particular, tell your doctor:

• if you have epilepsy. Treatment with Escitalopram should be stopped if seizures

  • occur for the same time or if there is an increase in the seizure frequency (see also section 4 “Possible side effects”).

• if you suffer from impaired liver or kidney function. Your doctor may need to adjust

  • your dosage.

• if you have diabetes. Treatment with Escitalopram may alter glycaemic control.

  • Insulin and/or oral hypoglycaemic dosage may need to be adjusted.
• If you have a decreased level of sodium in the blood.

• if you have a tendency to easily develop bleedings or bruises, or if you are pregnant

  • (see ‘Pregnancy, breastfeeding and fertility’).
• if you are receiving electroconvulsive treatment.
• If you have coronary heart disease.

• If you suffer or have suffered from heart problems or have recently had a heart

  • attack.

• If you have a low resting heart rate and/or you know that you may have salt

  • depletion as a result of prolonged severe diarrhoea and vomiting (Being sick) or usage of diuretics (water tablets).

• If you experience a fast or irregular heartbeat, fainting, collapse or dizziness on

  • standing up, which may indicate abnormal functioning of the heart rate.

• If you have or have previously had eye problems, such as certain kinds of

  • glaucoma (increased pressure in the eye).

Please note

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

Symptoms such as restlessness or difficulty to sit or stand still can also occur during the first weeks of the treatment. Tell your doctor immediately if you experience these symptoms.

Medicines like Escitalopram (so called SSRIs/SNRIs) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms have continued after stopping treatment.

Thoughts of suicide and worsening of your depression or anxiety disorder

If you are depressed and/or have anxiety disorders you can sometimes have thoughts of harming or killing yourself. These may be increased when first starting antidepressants, since these medicines all take time to work, usually about two weeks but sometimes longer.

You may be more likely to think like this:

• If you have previously had thoughts about killing or harming yourself.

• If you are a young adult. Information from clinical trials has shown an increased risk

  • of suicidal behaviour in adults aged less than 25 years with psychiatric conditions who were treated with an antidepressant.

If you have thoughts of harming or killing yourself at any time, contact your doctor or go to a hospital straight away.

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 might ask them to tell you if they think your depression or anxiety is getting worse, or if they are worried about changes in your behaviour.

Use in children and adolescents

Escitalopram should normally not be used for children and adolescents under 18 years. Also, you should know that patients under 18 have an increased risk of side effects such as suicide attempts, suicidal thoughts and hostility (predominately aggression, oppositional behaviour and anger) when they take this class of medicines. Despite this, your doctor may prescribe Escitalopram for patients under 18 because he/she decides that this is in their best interest. If your doctor has prescribed Escitalopram for a patient under 18 and you want to discuss this, please go back to your doctor. You should inform your doctor if any symptoms listed above develop or worsen when patients under 18 are taking Escitalopram. Also, the long-term safety effects concerning growth, maturation and cognitive and behavioural development of Escitalopram in this age group have not yet been demonstrated.

Other medicines and Escitalopram

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

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

• “Non-selective monoamine oxidase inhibitors (MAOIs)”, containing phenelzine,

  • iproniazid, isocarboxazid, nialamide, and tranylcypromine as active ingredients. If you have taken any of these medicines, you will need to wait 14 days before you start taking Escitalopram. After stopping Escitalopram, you must allow 7 days before taking any of these medicines.

• “Reversible, selective MAO-A inhibitors”, containing moclobemide (used to treat

  • depression).

• “Irreversible MAO-B inhibitors”, containing selegiline (used to treat Parkinson’s

  • disease). These increase the risk of side effects.
• The antibiotic linezolid.
• Lithium (used in the treatment of manic-depressive disorder) and tryptophan.
• Imipramine and desipramine (both used to treat depression).

• Sumatriptan and similar medicines (used to treat migraine) and tramadol and

  • similar medicines (opioids, used against severe pain). These increase the risk of side effects.

• 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 increased blood levels of Escitalopram.
• St. John’s Wort (Hypericum perforatum) - a herbal remedy used for depression.

• Acetylsalicylic acid and non-steroidal anti-inflammatory drugs (medicines used

  • for pain relief or to thin the blood, so called anti-coagulant). These may increase bleeding-tendency.

• Warfarin, dipyridamole, and phenprocoumon (medicines used to thin the blood, so

  • called anticoagulant). Your doctor will probably check the coagulation time of your blood when starting and discontinuing Escitalopram in order to verify that your dose of anti-coagulant is still adequate.

• Mefloquine (used to treat Malaria), bupropion (used to treat depression) and

  • tramadol (used to treat severe pain) due to a possible risk of a lowered threshold for seizures.

• Neuroleptics (medicines to treat schizophrenia, psychosis) and antidepressants

  • (tricyclic antidepressants and SSRIs) due to a possible risk of a lowered threshold for seizures.

• Flecainide, propafenone, and metoprolol (used in cardiovascular diseases)

  • clomipramine, and nortriptyline (antidepressants) and risperidone, thioridazine, and haloperidol (antipsychotics). The dosage of Escitalopram may need to be adjusted.

• Medicines that decrease blood levels of potassium or magnesium, as these

  • conditions increase the risk of life-threatening heart rhythm disorder.

Do not take Escitalopram if you take medicines for heart rhythm problems or medicines that may affect the heart’s rhythm, such as Class IA and III antiarrhythmics, antipsychotics (e.g. phenothiazine derivatives, pimozide, haloperidol), tricyclic antidepressants, certain antimicrobial agents (e.g. sparfloxacin, moxifloxacin, erythromycin IV, pentamidine, anti-malarial treatment particularly halofantrine), certain antihistamines (e.g. astemizole, hydroxyzine, mizolastine). If you have any further questions about this you should speak to your doctor.

Escitalopram with food, drink and alcohol

Escitalopram can be taken with or without food (see section 3 “How to take Escitalopram”).

As with many medicines, combining Escitalopram with alcohol is not advisable, although Escitalopram is not expected to interact with alcohol.

Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. Do not take Escitalopram if you are pregnant or breast-feeding, unless you and your doctor have discussed the risks and benefits involved.

If you take Escitalopram during the last 3 months of your pregnancy you should be aware that the following effects may be seen in your newborn baby: trouble with breathing, bluish skin, fits, body temperature changes, feeding difficulties, vomiting, low blood sugar, stiff or floppy muscles, vivid reflexes, tremor, jitteriness, irritability, lethargy, constant crying, sleepiness and sleeping difficulties. If your newborn baby has any of these symptoms, please contact your doctor immediately.

Make sure your midwife and/or doctor know you are on Escitalopram. When taken during pregnancy, particularly in the last 3 months of pregnancy, medicines like Escitalopram may increase the risk of a serious condition in babies, called persistent pulmonary hypertension of the newborn (PPHN), making the baby breathe faster and appear bluish. These symptoms usually begin 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 take Escitalopram near the end of your pregnancy there may be an increased risk of heavy vaginal bleeding shortly after birth, especially if you have a history of bleeding disorders. Your doctor or midwife should be aware that you are taking Escitalopram so they can advise you.

If used during pregnancy Escitalopram should never be stopped abruptly.

It is expected that Escitalopram will be excreted into breast milk.

Citalopram, a medicine like Escitalopram, has been shown to reduce the quality of sperm in animal studies. Theoretically, this could affect fertility, but impact on human fertility has not been observed as yet.

Driving and using machines

You are advised not to drive a car or operate machinery until you know how Escitalopram affects you.

Escitalopram contains sodium

This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.

3.

How to take Escitalopram

Always take Escitalopram exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

Adults

Depression

The normally recommended dose of Escitalopram is 10 mg taken as one daily dose. The dose may be increased by your doctor to a maximum of 20 mg per day.

Panic disorder

The starting dose of Escitalopram is 5 mg as one daily dose for the first week before increasing the dose to 10 mg per day. The dose may be further increased by your doctor to a maximum of 20 mg per day.

Social anxiety disorder

The normally recommended dose of Escitalopram is 10 mg taken as one daily dose. Your doctor can either decrease your dose to 5 mg per day or increase the dose to a maximum of 20 mg per day, depending on how you respond to the medicine.

Generalised anxiety disorder

The normally recommended dose of Escitalopram is 10 mg taken as one daily dose. The dose may be increased by your doctor to a maximum of 20 mg per day.

Back Side

Obsessive-compulsive disorder

The normally recommended dose of Escitalopram is 10 mg taken as one daily dose. The dose may be increased by your doctor to a maximum of 20 mg per day.

Elderly patients (above 65 years of age)

The recommended starting dose of Escitalopram is 5 mg taken as one daily dose. The dose may be increased by your doctor to 10 mg per day.

Use in children and adolescents

Escitalopram should not normally be given to children and adolescents. For further information please see section 2 “Warnings and precautions”.

Reduced kidney function

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

Reduced liver function

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

Patients known to be poor metabolisers of the enzyme CYP2C19

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

How to take the tablets

You can take Escitalopram with or without food.

Escitalopram Orodispersible tablets should be handled with care. Do not handle the tablets with wet hands because they may fall apart.

Carefully remove the tablet. Put the tablet on your tongue. The tablet will disintegrate quickly and can be swallowed without water.

The score line is not intended for breaking the tablet.

Duration of treatment

It may take a couple of weeks before you start to feel better. Continue to take Escitalopram even if it takes some time before you feel any improvement in your condition.

Do not change the dose of your medicine without talking to your doctor first.

Continue to take Escitalopram for as long as your doctor recommends. If you stop your treatment too soon, your symptoms may return. It is recommended that treatment should be continued for at least 6 months after you feel well again.

If you take more Escitalopram than you should

If you take more than the prescribed dose of Escitalopram, contact your doctor or nearest hospital emergency department immediately. Do this even if there are no signs of discomfort. Some of the signs of an overdose could be dizziness, tremor, agitation, convulsion, coma, nausea, vomiting, change in heart rhythm, decreased blood pressure and change in body fluid/salt balance. Take the Escitalopram box/ container with you when you go to the doctor or hospital.

If you forget to take Escitalopram

Do not take a double dose to make up for forgotten doses. If you do forget to take a dose, and you remember before you go to bed, take it straight away. Carry on as usual the next day. If you only remember during the night, or the next day, leave out the missed dose and carry on as usual.

If you stop taking Escitalopram

Do not stop taking Escitalopram until your doctor tells you to do so. When you have completed your course of treatment, it is generally advised that the dose of Escitalopram is gradually reduced over a number of weeks.

When you stop taking Escitalopram, especially if it is abruptly, you may feel discontinuation symptoms. These are common when treatment with Escitalopram is stopped. The risk is higher, when Escitalopram has been used for a long time or in high doses or when the dose is reduced too quickly. Most people find that the symptoms are mild and go away on their own within two weeks. However, in some patients they may be severe in intensity or they may be prolonged (2-3 months or more). If you get severe discontinuation symptoms when you stop taking Escitalopram, please contact your doctor. He or she may ask you to start taking your tablets again and come off them more slowly.

Discontinuation symptoms include: Feeling dizzy (unsteady or off-balance), feelings like pins and needles, burning sensations and (less commonly) electric shock sensations, including in the head, sleep disturbances (vivid dreams, nightmares, inability to sleep), feeling anxious, headaches, feeling sick (nausea), sweating (including night sweats), feeling restless or agitated, tremor (shakiness), feeling confused or disorientated, feeling emotional or irritable, diarrhoea (loose stools), visual disturbances, fluttering or pounding heartbeat (palpitations).

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

4.

Possible side effects

Like all medicines, Escitalopram can cause side effects, although not everybody gets them.

The side effects usually disappear after a few weeks of treatment. Please be aware that many of the effects may also be symptoms of your illness and therefore will improve when you start to get better.

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

Uncommon (may affect up to 1 in 100 people):

• Unusual bleeds, including gastrointestinal bleeds Rare (may affect up to 1 in 1000

  • people):

• Swelling of skin, tongue, lips, pharynx or face, hives or have difficulties breathing

  • or swallowing (serious allergic reaction).

• High fever, agitation, confusion, trembling and abrupt contractions of muscles

  • these may be signs of a rare condition called serotonin syndrome.

Not known (frequency cannot be estimated from the available data):

• Difficulties urinating
• Seizures (fits), see also section 2 “Warnings and precautions”

• Yellowing of the skin and the white in the eyes are signs of liver function impairment/

  • hepatitis

• Fast, irregular heartbeat, fainting which could be symptoms of a life-threatening

  • condition known as Torsade de Pointes

• Thoughts of harming yourself or killing yourself, see also section 2 “Warnings and

  • precautions”
• Sudden swelling of skin or mucosa (angioedemas)

In addition to above the following side effects have been reported:

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

• Feeling sick (nausea)
• Headache

Common (may affect up to 1 in 10 people):

• Blocked or runny nose (sinusitis)
• Decreased or increased appetite

• Anxiety, restlessness, abnormal dreams, difficulties falling asleep, feeling sleepy,

  • dizziness, yawning, tremors, prickling of the skin
• Diarrhoea, constipation, vomiting, dry mouth
• Increased sweating
• Pain in muscle and joints (arthralgia and myalgia)

• Sexual disturbances (delayed ejaculation, problems with erection, decreased

  • sexual drive and women may experience difficulties achieving orgasm)

    • Fatigue, fever
    • Increased weight

Uncommon (may affect up to 1 in 100 people):

• Nettle rash (urticaria), rash, itching (pruritus)
• Grinding one’s teeth, agitation, nervousness, panic attack, confusion
• Disturbed sleep, taste disturbance, fainting (syncope)
• Enlarged pupils (mydriasis), visual disturbance, ringing in the ears (tinnitus)
• Loss of hair
• Excessive menstrual bleeding
• Irregular menstrual period
• Decreased weight
• Fast heart beat
• Swelling of the arms or legs
• Nosebleeds

Rare (may affect up to 1 in 1000 people):

• Aggression, depersonalisation, hallucination
• Slow heart beat

Not known (frequency cannot be estimated from the available data):

• Decreased levels of sodium in the blood (the symptoms are feeling sick and unwell

  • with weak muscles or confused)
• Dizziness when you stand up due to low blood pressure (orthostatic hypotension)
• Abnormal liver function test (increased amounts of liver enzymes in the blood)
• Movement disorders (involuntary movements of the muscles)
• Painful erections (priapism)

• Signs of abnormal bleeding e.g. from skin and mucous (ecchymosis) and low level

  • of blood platelets (thrombocytopenia)

• Increased secretion of a hormone called ADH, causing the body to retain water

  • and dilute the blood, reducing the amount of sodium (inappropriate ADH secretion)
• Increased blood levels of the hormone prolactin
• Flow of milk in men and in women that are not nursing
• Mania

• An increased risk of bone fractures has been observed in patients taking this type

  • of medicines.

• Alteration of the heart rhythm (called “prolongation of QT interval”, seen on ECG,

  • measuring electrical activity of the heart).

• Heavy vaginal bleeding shortly after birth (postpartum haemorrhage), see

  • ‘Pregnancy, breast-feeding and fertility’ in section 2 for more information.

In addition, a number of side effects are known to occur with drugs that work in a similar way to Escitalopram (the active ingredient of Escitalopram).

These are:

• Motor restlessness (akathisia)
• Loss of appetite

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.

You can help to make sure that medicines remain as safe as possible by reporting any unwanted side effects via the internet at www.mhra.gov.uk/yellowcard. Alternatively, you can call Freephone 0808 100 3352 (available from 10 a.m. to 2 p.m. Mondays to Fridays) or fill in a paper form available from your local pharmacy.

You can also search for MHRA Yellow Card in the Google Play and Apple App store. By reporting side effects, you can help provide more information on the safety of this medicine.

5.

How to store Escitalopram

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

Do not use Escitalopram after the expiry date, which is stated on the label or carton after EXP.

The expiry date refers to the last day of that month.

Store in the original package to protect from moisture.

This medicine does not require any special temperature storage conditions.

Do not throw away any medicine via wastewater or household waste. Ask your pharmacist how to throw away any medicines you no longer use. These measures will help to protect the environment.

6.

Contents of the pack and other information

What Escitalopram contains

The active substance is Escitalopram.

Each Escitalopram 10 mg Orodispersible Tablets tablet contains 10 mg Escitalopram (as oxalate).

Each Escitalopram 15 mg Orodispersible Tablets tablet contains 15 mg Escitalopram (as oxalate).

Each Escitalopram 20 mg Orodispersible Tablets tablet contains 20 mg Escitalopram (as oxalate).

The other ingredients are: Microcrystalline cellulose; Silicified Microcrystalline Cellulose; Croscarmellose Sodium; Colloidal Anhydrous Silica; Sucralose; Peppermint Flavour; Orange Flavour; Talc Micronized and Magnesium stearate.

What Escitalopram looks like and contents of the pack

10 mg: White to off white, capsule shaped, biconvex, uncoated tablets, debossed "4" on one side with score line on both sides.

15 mg: White to off white, capsule shaped, biconvex, uncoated tablets, debossed "5" on one side with score line on both sides.

20 mg: White to off white, capsule shaped, biconvex, uncoated tablets, debossed "6" on one side with score line on both sides.

Escitalopram 10 mg, 15 mg and 20 mg Orodispersible Tablets are available in aluminium-aluminium blister packs with containing 28 or 56 Orodispersible tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Zydus Pharmaceuticals UK Ltd

Sandretto Building Weedon

Northampton NN7 4PP UK

This leaflet was last revised in Dec-2025.

To request a copy of this leaflet in Braille, large print or audio format, contact the licence holder at the above address or telephone: 0800 9956034 / email: DrugSafety@ZydusUK.com

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