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Amitriptyline Hydrochloride 10 mg film-coated tablets – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
10 mg
Contains active substance:

Patient leaflet - Amitriptyline Hydrochloride 10 mg film-coated tablets

1. What Amitriptyline hydrochloride is and what it is used for

Amitriptyline hydrochloride belongs to a group of medicines called tricyclic antidepressants.

This medicine is used to treat:

  • Depression in adults (major depressive episodes)
  • Neuropathic pain in adults
  • Chronic tension type headache prophylaxis in adults
  • Migraine prophylaxis in adults
  • Bed-wetting at night in children aged 6 years and above, only when organic

    causes, such as spina bifida and related disorders, have been excluded and no response has been achieved to all other non-drug and drug treatments, including muscle relaxants and desmopressin. This medicine should only be prescribed by doctors with expertise in treating patients with persistent bed-wetting.

2. What you need to know before you take Amitriptyline hydrochloride

Do not take Amitriptyline hydrochloride

  • if you are allergic to Amitriptyline hydrochloride or any of the other ingredients of

    this medicine (listed in section 6)

  • if you recently have had a heart attack (myocardial infarction)
  • if you have heart problems such as disturbances in heart rhythm which are seen on

    an electrocardiogram (ECG), heart block, or coronary artery disease

  • if you are taking medicines known as monoamine oxidase inhibitors (MAOIs)
  • if you have taken MAOIs within the last 14 days
  • if you have taken moclobemide the day before
  • if you have a severe liver disease.

If you are treated with Amitriptyline hydrochloride, you have to stop taking this medicine and wait for 14 days before you start treatment with a MAOI.

This medicine should not be used for children below 6 years of age.

Warning and precautions

Talk to your doctor or pharmacist before taking Amitriptyline hydrochloride.

Serious cutaneous reactions including drug reaction with eosinophilia and systemic symptoms (DRESS) have been reported in association with Amitriptyline hydrochloride treatment. Stop using Amitriptyline hydrochloride and seek medical attention immediately if you notice any of the symptoms related to these serious cutaneous reactions described in section 4.

The use of buprenorphine/opioids together with Amitriptyline hydrochloride tablets can lead to serotonin syndrome, a potentially life-threatening condition (see “Other medicines and Amitriptyline hydrochloride tablets").

Heart rhythm disorders and hypotension may occur if you receive a high dosage of Amitriptyline. This might also occur in usual doses if you have pre-existing heart disease.

Prolonged QT interval

A heart problem called “prolonged QT interval” (which is shown on your electrocardiogram, ECG) and heart rhythm disorders (rapid or irregular heart beat) have been reported with Amitriptyline hydrochloride. Tell your doctor if you: · have slow heart rate,

  • have or had a problem where your heart cannot pump the blood round your body

    as well as it should (a condition called heart failure),

  • are taking any other medication that may cause heart problems, or · have a problem that gives you a low level of potassium or magnesium, or a high

    level of potassium in your blood,

  • have a surgery planned as it might be necessary to stop the treatment with

    Amitriptyline hydrochloride before you are given anaesthetics. In the case of acute surgery, the anaesthetist should be informed about the treatment of Amitriptyline hydrochloride,

  • have an over active thyroid gland or receive thyroid medication.

Thoughts of suicide and worsening of your depression

If you are depressed, you can sometimes have thoughts of harming or killing yourself. These may be increased when first starting antidepressant, since these medicines all take time to work, usually about two week 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 young 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, 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.

Episodes of mania

Some patients with manic-depressive illness may enter into a manic phase. This is characterized by profuse and rapidly changing ideas, exaggerated gaiety and excessive physical activity. In such cases, it is important to contact your doctor who probably will change your medication.

Tell your doctor if you have, or have had in the past, any medical problems, especially if you have

  • narrow angle glaucoma (loss of vision due to abnormally high pressure in the eye) · epilepsy, a history of convulsions or fits
  • difficulty in passing urine
  • enlarged prostate
  • thyroid disease
  • bipolar disorder
  • schizophrenia
  • severe liver disease
  • severe heart disease
  • pylorus stenosis (narrowing of the gastric outlet) and paralytic ileus (blocked

    intestine)

  • diabetes as you might need and adjustment of your antidiabetic medicine. If you use antidepressants such as SSRIs, your doctor might consider changing the dose of your medicine (see also section 2 Other medicines and Amitriptyline hydrochloride and section 3)

Elderly are more likely to suffer from certain side effects, such as dizziness when you stand up due to low blood pressure (see also section 4 Possible side effects).

Children and adolescents

Depression, neuropathic pain, chronic tension type headache and migraine prophylaxis

Do not give this medicine to children and adolescents aged below 18 years for these treatments as safety and efficacy have not been established in this age group. Bed-wetting at night

  • An ECG should be performed prior to initiating therapy with amitriptyline to

    exclude long QT syndrome

    • This medicines should not be taking at the same time as an anticholinergic drug

      (see also section 2 Other medicines and Amitriptyline hydrochloride) · Suicidal thoughts and behaviours may also develop during early treatment with antidepressants for disorders other than depression; the same precautions observed when treating patients with depression should therefore be followed when treating patients with enuresis

Other medicines and Amitriptyline hydrochloride

Some medicines may affect the action of other medicines and this can sometimes cause serious side effects.

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

  • monoamine oxidase inhibitors (MAOIs) e.g. phenelzine, iproniazid, isocarboxazid, nialamide or tranylcypromine (used to treat depression) or selegiline (used to treat Parkinson's disease). These should not be taken at the same time as Amitriptyline hydrochloride (see section 2 Do not take Amitriptyline hydrochloride)
  • adrenaline, ephedrine, isoprenaline, noradrenaline, phenylephrine and phenylpropanolamine (these may be present in cough or cold medicine, and in some anaesthetics)
  • medicine to treat high blood pressure for example calcium-channel blockers (e.g.

    diltiazem and verapamil), guanethidine, betanidine, clonidine reserpine and methyldopa

  • Anticholinergic drugs such as certain medicines to treat Parkinsons disease and gastrointerstinal disorders (e.g. atropine, hyoscyamine)
  • thioridazine (used to treat schizophrenia)
  • tramadol (painkiller)
  • medicines to treat fungal infections (e.g. fluconazole, terbinafine, ketoconazole, and itraconazole)
  • sedatives (e.g. babiturates)
  • antidepressants (e.g SSRIs (fluoxetine, paroxetine, fluvoxamine), duloxetine and bupropion)
  • buprenorphine/opioids may interact with Amitriptyline and you may experience symptoms such as involuntary, rhythmic contractions of muscles, including the muscles that control movement of the eye, agitation, hallucinations, coma, excessive sweating, tremor, exaggeration of reflexes, increased muscle tension, body temperature above 38°C. Contact your doctor when experiencing such symptoms.
  • medicines for certain heart conditions (e.g. beta blockers and antiarrhythmics) · cimetidine (used to treat stomach ulcers)
  • methylphenidate (used to treat ADHD)
  • ritonavir (used to treat HIV)
  • Oral contraceptives
  • rifampicin (to treat infections)
  • phenytoin and carbamazepine (used to treat epilepsy)
  • St. John´s Wort (hypericum perforatum) – a herbal remedy used for depression · thyroid medication.
  • Valproic acid

You should also tell your doctor if you take or have recently taken medicine that may affect the heart´s rhythm. e.g.:

  • medicines to treat irregular heartbeats (e.g. quinidine and sotalol) · astemizole and terfenadine (used to treat allergies and hayfever) · medicines used to treat some mental illnesses (e.g. pimozide and sertindole) · cisapride (used to treat certain types of indigestion)
  • halofantrine (used to treat malaria)
  • methadone (used to treat pain and for detoxification)
  • diuretics (“water tablets” e.g. furosemide)

If you are going to have an operation and receive general or local anaesthetics, you should tell your doctor that you are taking this medicine.

Likewise, you should tell your dentist that you take this medicine if you are to receive a local anaesthetic.

Amitriptyline hydrochloride with food, drink and alcohol

It is not advised to drink alcohol during treatment with this medicine as it might increase the sedative effect.

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.

Amitriptyline is not recommended during pregnancy unless your doctor considers it clearly necessary and only after careful consideration of the benefit and risk. If you have taken this medicine during the last part of the pregnancy, the newborn may have withdrawal symptoms such as irritability, increased muscle tension, tremor, irregular breathing, poor drinking, loud crying, urinary retention, and constipation Your doctor will advise you whether to start/continue/stop breast-feeding, or stop using this medicine taking into account the benefit of breast-feeding for your child and the benefit of therapy for you.

Driving and using machines

This medicine may cause drowsiness and dizziness, especially in the beginning of the treatment. Do not drive or work with tools or machinery if you are affected.

Amitriptyline hydrochloride contains Lactose

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

Amitriptyline hydrochloride 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 Amitriptyline hydrochloride

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

Not all dosage regimens can be achieved with all dosage forms/strengths. The appropriate dosage form/strength should be selected for initial doses and for any increases in subsequent doses.

Depression

Adults

The recommended initial dose is 25 mg two times daily.

Depending on the response to the medicine, your doctor may gradually increase the dose to 150 mg per day divided in two doses.

Elderly (above 65 years of age) and patients with cardiovascular disease

The recommended initial dose is 10 mg – 25 mg daily.

Depending on your response to the medicine, your doctor may gradually increase the dose to a total daily dose of 100 mg divided in two doses. If you receive doses in the range of 100 mg – 150 mg, your doctor may need to do more frequent follow-up with you.

Use in children and adolescents

This medicine should not be given to children or adolescents for treatment of depression. For further information please see section 2.

Neuropathic pain, chronic tension type headache and migraine prophylaxis

Your doctor will adjust the medication according to your symptoms and your response to the treatment.

Adults

The recommended initial dose is 10 mg - 25 mg in the evening.

The recommended daily dose is 25 mg - 75 mg.

Depending on your response to the medicine, your doctor may gradually increase the dose. If you receive doses above 100 mg daily, your doctor may need to do more frequent follow-up with you. Your doctor will instruct you whether to take the doses once daily or divide into two doses.

Elderly (above 65 years of age) and patients with cardiovascular disease The recommended initial dose is 10 mg – 25 mg in the evening.

Depending on your response to the medicine, your doctor may gradually increase the dose. If you receive doses above 75 mg daily, your doctor may need to do more frequent follow-up with you.

Use in children and adolescents

This medicine should not be given to children or adolescents for treatments of neuropathic pain, chronic tension type headache prophylaxis and migraine prophylaxis. For further information please see section 2.

UK (Unit-V) Amitriptyline hydrochloride Leaflet

Version: 00

Dimension: 240 x 580 mm

1025 1026

Supersede: 2086013

Bed-wetting at night

Use in children and adolescents

The recommended doses for children:

  • aged below 6 years: see section 2 Do not take Amitriptyline hydrochloride · aged 6 to 10 years: 10 mg – 20 mg daily. A suitable dosage form should be used

    for this age group.

  • aged 11 years and above: 25 mg – 50 mg.

The dose should be increased gradually.

Take this medicine 1-1½ hours before bedtime.

Before starting treatment, your doctor will conduct an ECG of your heart to check for sign of unusual heartbeat.

Your doctor will re-evaluate your treatment after 3 months and if needed perform a new ECG

Do not stop the treatment without consulting your doctor first.

Patients with special risks

Patients with liver diseases or people known as “poor metabolisers” usually receive lower doses.

Your doctor may take blood samples to determine the level of Amitriptyline hydrochloride in the blood (see also section 2).

How and when to take Amitriptyline hydrochloride

This medicine can be taken with or without food.

Swallow the tablets with a drink of water. Do not chew them.

Duration of treatment

Do not change the dose of the medicine or stop taking the medicine without consulting your doctor first.

Depression

As with other medicines for the treatment of depression it may take a few weeks before you feel any improvement.

In treating depression the duration of treatment is individual, and is usually at least 6 months. The duration of treatment is decided by your doctor.

Continue to take this medicine for as long as your doctor recommends.

The underlying illness may persist for a long time. If you stop your treatment too soon, your symptoms may return.

Neuropathic pain, chronic tension type headache and migraine prophylaxis

It might take a few weeks before your feel any improvement of your pain.

Talk to your doctor about the duration of your treatment and continue to take this medicine for as long as your doctor recommends.

Bed-wetting at night

Your doctor will evaluate if the treatment should be continued after 3 months.

If you take more Amitriptyline hydrochloride than you should

Contact your doctor or nearest hospital casualty department immediately. Do this even if there are no signs of discomfort or poisoning. Take the container of this medicine with you if you go to a doctor or hospital.

Symptoms of overdose include:

  • dilated pupils
  • fast or irregular heartbeats
  • difficulties passing water
  • dry mouth and tongue
  • intestinal blockage
  • fits
  • fever
  • agitation
  • confusion
  • hallucinations
  • uncontrolled movements
  • low blood pressure, weak pulse, pallor
  • difficulty breathing
  • blue discolouration of the skin
  • decreased heart rate
  • drowsiness
  • loss of consciousness
  • coma
  • various cardiac symptoms such as heart block, heart failure, hypotension,

    cardiogenic shock, metabolic acidosis, hypokalemia.

Overdose with Amitriptyline hydrochloride in children could have serious consequences. Children are especially susceptible to coma, cardiac symptoms, difficulty in breathing, seizures, low blood sodium level, lethargy, drowsiness, nausea, vomiting and high blood sugar level.

If you forget to take Amitriptyline hydrochloride

Take the next dose at the usual time. Do not take a double dose to make up for a forgotten dose.

If you stop taking Amitriptyline hydrochloride

Your doctor will decide when and how to stop your treatment to avoid any unpleasant symptoms that might occur if it is stopped abruptly (e.g. headache, feeling unwell, sleeplessness and irritability).

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

4. Possible side effects

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

If you get any of the following symptoms you should see your doctor immediately:

  • Attacks of intermittent blurring of vision, rainbow vision, and eye pain. You should immediately have an eye examination before the treatment with this

    medicine can be continued. This condition may be signs of acute glaucoma. Very rare side effect, may affect up to 1 in 10,000 people.

  • A heart problem called "prolonged QT interval" (which is shown on your

    electrocardiogram, ECG). Common side effect, may affect up to 1 in 10 people.

  • Bad constipation, a swollen stomach, fever and vomiting.

    These symptoms may be due to parts of the intestine becoming paralysed. Rare

    side effect, may affect up to 1 in 1,000 people.

  • Any yellowing of the skin and the white in the eyes (jaundice). Your liver may be affected. Rare side effect, may affect up to 1 in 1,000 people.
  • Bruising, bleeding, pallor or persistent sore throat and fever. These symptoms can be the first signs that your blood or bone marrow may be

    affected.

    Effects on the blood could be a decrease in the number of red cells (which carry

    oxygen around the body), white cells (which help to fight infection) and platelets (which help with clotting). Rare side effect, may affect up to 1 in 1,000 people.

  • Suicidal thoughts or behaviour. Rare side effect, may affect up to 1 in 1,000

    people.

  • Signs of a severe allergic reaction (anaphylaxis) such as swelling of your tongue

    or face, or difficulty breathing.

Side effects listed below have been reported in the following frequencies:

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

  • sleepiness/drowsiness
  • shakiness of hands or other body parts
  • dizziness
  • headache
  • irregular, hard, or rapid heartbeat
  • dizziness when you stand up due to low blood pressure (orthostatic hypotension) · dry mouth
  • constipation
  • nausea
  • excessive sweating
  • weight gain
  • slurred or slow speech

    • aggression
    • congested nose.

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

  • confusion
  • sexual disturbances (decreased sex-drive, problems with erection) · disturbance in attention
  • changes in taste
  • numbness or tingling in the arms or legs
  • disturbed coordination
  • dilated pupils
  • heart block
  • fatigue
  • low sodium concentration in the blood
  • agitation
  • urination disorders
  • feeling thirsty.

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

  • excitement, anxiety, difficulties sleeping, nightmares
  • convulsions
  • tinnitus
  • increased blood pressure
  • diarrhoea, vomiting
  • skin rash, nettle rash (urticarial), swelling of the face and tongue · difficulties passing urine
  • increased production of breast milk or breast milk outflow without breast feeding · increased pressure in the eye ball
  • collapse conditions
  • worsening of cardiac failure
  • liver function impairment (e.g. cholestatic liver disease).

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

  • decreased appetite
  • delirium (especially in elderly patients), hallucinations
  • abnormality in the heart's rhythm, or heartbeat pattern
  • swelling of the salivary glands
  • hair loss
  • increased sensitivity to sunlight
  • breast enlargement in men
  • fever
  • weight loss
  • abnormal results of liver function tests.

Very rare: (may affect up to 1 in 10,000 people)

  • heart muscle disease
  • feeling of inner restlessness and a compelling need to be in constant motion · disorder of the peripheral nerves
  • acute increase of pressure in the eye
  • particular forms of abnormal heart rhythm (so called torsades de pointes) · allergic inflammation of the lung alveoli and of the lung tissue.

Not known (frequency cannot be estimated from available data): · absent sensation of appetite

  • elevation or lowering of blood sugar levels
  • paranoia
  • movement disorders (involuntary movements or decreased movements) · hypersensitivity inflammation of heart muscle
  • hepatitis
  • hot flush
  • Dry eyes
  • Stop using amitriptyline hydrochloride and seek medical attention immediately if you notice any of the following symptoms:
  • Widespread rash, high body temperature and enlarged lymph nodes (DRESS or drug hypersensitivity syndrome).

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

Reporting of side effects

If you get any side effects talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via Yellow Card Scheme website www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

By reporting side effects, you can help provide more information on the safety of this medicine.

5. How to store Amitriptyline hydrochloride

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

Do not use this medicine after the expiry date which is stated on the outer carton and blister after EXP. The expiry date refers to the last day of that month.

This medicine does not require any special storage conditions.

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

6. Contents of the pack and other information

What Amitriptyline hydrochloride contains

The active substance is amitriptyline hydrochloride.

Each film-coated tablet contains 10 mg amitriptyline hydrochloride. Each film-coated tablet contains 25 mg amitriptyline hydrochloride. Each film-coated tablet contains 50 mg amitriptyline hydrochloride.

The other ingredients are:

Tablet core: Lactose monohydrate, cellulose microcrystalline, sodium starch glycolate, silica, colloidal anhydrous & magnesium stearate.

Tablet coating: Hypromellose (E464), polyethylene glycol (E1521), talc (E553b), titanium dioxide (E171).

What Amitriptyline hydrochloride looks like and contents of the pack

Amitriptyline hydrochloride 10 mg film-coated tablets White to off-white, round shaped, biconvex film coated tablets, debossed with “H1” on one side and “TL” on the other side.

Amitriptyline hydrochloride 25 mg film-coated tablets

White to off-white, round shaped, biconvex film coated tablets debossed with “H2” on one side and “TL” on the other side.

Amitriptyline hydrochloride 50 mg film-coated tablets

White to off-white, round shaped, biconvex film coated tablets debossed with “H3” on one side and “TL” on the other side.

Blister pack containing 28 and 100 film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Amarox Limited

Congress House, 14 Lyon Road

Harrow, HA1 2EN

United Kingdom

This leaflet was last revised in 05/2025.

2087864

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 49445/0217

Last revision stated in the text: May 2025 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Amitriptyline Hydrochloride 10 mg film-coated tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Amitriptyline
Strength 10 mg
Pharmaceutical form Oral tablet
How is it taken Oral
Pack sizes 28 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Drug group (ATC)
  1. N Nervous system drugs
    1. N06 Psychoanaleptics
      1. N06A Antidepressants
        1. N06AA Non-selective monoamine reuptake inhibitors
          1. N06AA09 amitriptyline
Marketing authorisation PL 49445/0217
Codes GTIN 5060608564729 · BNF 04030100

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.