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Varenicline 1 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:
1 mg
Other strengths and forms:
Contains active substance:

Patient leaflet - Varenicline 1 mg film-coated tablets

1. What Varenicline is and what it is used for

Varenicline tablets contains the active substance varenicline. Varenicline is a medicine which is used in adults to help them stop smoking.

Varenicline can help to relieve the craving and withdrawal symptoms associated with stopping smoking.

Varenicline can also reduce the enjoyment of cigarettes if you do smoke when on treatment.

2. What you need to know before you take Varenicline

Do not take Varenicline:

If you are allergic to varenicline or any of the other ingredients of this medicine (listed in section 6)

Warnings and precautions

Talk to your doctor or pharmacist before taking Varenicline.

There have been reports of depression, suicidal thoughts and behaviour and suicide attempts in patients taking Varenicline. If you are taking Varenicline and develop agitation, depressed mood, changes in behaviour that are of concern to you or your family or if you develop suicidal thoughts or behaviours stop taking Varenicline and contact your doctor immediately for treatment assessment.

The effects of stopping smoking

The effects of changes in your body resulting from stopping smoking, with or without treatment with Varenicline, may alter the way other medicines work. Therefore, in some cases an adjustment of the dose may be necessary. See below under 'Other medicines and Varenicline' for further details.

For some people, stopping smoking with or without treatment has been associated with an increased risk of experiencing changes in thinking or behaviour, feelings of depression and anxiety and can be associated with a worsening of psychiatric disorder. If you have a history of psychiatric disorder you should discuss this with your doctor.

Heart symptoms

New or worse heart or blood vessel (cardiovascular) problems have been reported primarily in people who already have cardiovascular problems. Tell your doctor if you have any changes in symptoms during treatment with Varenicline. Get emergency medical help right away if you have symptoms of a heart attack or stroke.

Seizures

Tell your doctor if you have experienced seizures or have epilepsy before your start Varenicline treatment. Some people have reported seizures while taking Varenicline.

Hypersensitivity reactions

Stop taking Varenicline and tell your doctor immediately if you experience any of the following signs and symptoms that may indicate a serious allergic reaction: swelling of the face, lips, tongue, gums, throat or body and/or difficulty breathing, wheezing.

Skin reactions

Potentially life-threatening skin rashes (Stevens-Johnson syndrome and Erythema Multiforme) have been reported with the use of Varenicline. If you develop a rash or if your skin starts to peel or blister you should stop taking Varenicline and seek emergency medical help.

Children and adolescents

This medicine is not recommended for use in children and adolescents as efficacy was not demonstrated.

Other medicines and Varenicline

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

In some cases as a result of stopping smoking, with or without Varenicline, an adjustment of the dose of other medicines may be necessary. Examples include theophylline (a medicine to treat breathing problems), warfarin (a medicine to reduce blood clotting), and insulin (a medicine to treat diabetes). If in doubt, talk to your doctor or pharmacist.

If you have severe kidney disease you should avoid taking cimetidine (a medicine used for gastric problems) at the same time as Varenicline as this may cause increased blood levels of Varenicline.

Use of Varenicline with other therapies for smoking cessation

Consult your doctor before using Varenicline in combination with other smoking cessation therapies.

Varenicline with food and drink

There have been some reports of increased intoxicating effects of alcohol in patients taking varenicline. However, it is not known if varenicline actually increases alcohol intoxication.

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Pregnancy and breast-feeding

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.

It is preferable to avoid the use of Varenicline while you are pregnant. Talk to your doctor if you are intending to become pregnant.

Although it was not studied, this medicine may pass into breast milk. You should ask your doctor or pharmacist for advice before taking this medicine.

Driving and using machines

This medicine may be linked with dizziness, sleepiness and temporary loss of consciousness. Do not drive, operate complex machinery or engage in any other potentially hazardous activities until you know whether this medicine affects your ability to perform these activities.

Varenicline 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 Varenicline

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

You are more likely to stop smoking if you are motivated to stop. Ask your doctor or pharmacist for advice, support and sources of further information to help ensure your attempt to stop smoking is successful.

Before starting your course of Varenicline you should usually decide on a date in the second week of treatment (between day 8 and day 14) when you will stop smoking. If you are not willing or able to set a target quit date within 2 weeks, you may choose your own target quit date within 5 weeks after starting treatment. You should write this date on the pack as a reminder.

Varenicline comes as a white round tablet (0.5 mg) and a white capsule-shaped tablet (1 mg). You start with the white round tablet and then usually go to the white capsule-shaped tablet. See the chart below for the usual dosing instructions which you should follow from Day 1.

Week 1 Dose

Day 1-3 From day 1 to day 3, take one white round (Varenicline 0.5 mg film-coated tablet) once a day.

Day 4-7 From day 4 to day 7, take one white round (Varenicline 0.5 mg film-coated tablet) twice daily, once in the morning and once in the evening, at about the same time each day.

Week 2 Dose

Day 8-14 From day 8 to day 14, take one white capsule-shaped (Varenicline 1 mg film-coated tablet) twice daily, once in the morning and once in the evening, at about the same time each day.

Week 3-12 Dose

Day 15 - end of treatment

From day 15 until the end of treatment, take one white capsule-shaped (Varenicline 1 mg film-coated tablet) twice daily, once in the morning and once in the evening, at about the same time each day.

After 12 weeks of treatment, if you have stopped smoking, your doctor may recommend an additional 12 weeks of treatment with Varenicline 1 mg film-coated tablets twice daily to help avoid returning back to smoking.

If you are not able or willing to quit smoking straight away, reduce smoking during the first 12 weeks of treatment and quit by the end of that treatment period. Then continue to take Varenicline 1 mg film-coated tablets twice daily for a further 12 weeks resulting in a total of 24 weeks of treatment.

If you experience side effects that you cannot tolerate your doctor may decide to reduce your dose temporarily or permanently to 0.5 mg twice daily.

If you have problems with your kidneys, talk to your doctor before taking Varenicline. You may need a lower dose.

Varenicline is for oral use.

Swallow the tablets whole with water.

This medicine can be taken with or without food.

If you take more Varenicline than you should

If you accidentally take more Varenicline than your doctor prescribed, you must seek medical advice or go to the nearest hospital casualty department immediately. Take your box of tablets with you.

If you forget to take Varenicline

Do not take a double dose to make up for a forgotten tablet. It is important that you take Varenicline regularly at the same time each day. If you forget to take a dose, take it as soon as you remember. If, it is within 3-4 hours before your next dose, do not take the tablet that you have missed.

If you stop taking Varenicline

It has been shown in clinical trials that taking all doses of your medicine at the appropriate times and for the recommended duration of treatment described above will increase your chances of stopping smoking. Therefore, unless your doctor instructs you to stop treatment, it is important to keep taking Varenicline, according to the instructions described in the table above.

In smoking cessation therapy, risk of returning to smoking may be elevated in the period immediately following the end of treatment. You may temporarily experience increased irritability, urge to smoke, depression and/or sleep disturbances when you stop taking this medicine. Your doctor may decide to gradually lower your dose of Varenicline at the end of treatment.

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

Description
MA No.
Supplier SAP No.
New Supplier Code

Notes

Sign-offs

4. Possible side effects

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

Giving up smoking with or without treatment can cause various symptoms. These could include changes of mood (like feeling depressed, irritable, frustrated or anxious), sleeplessness, difficulty concentrating, decreased heart rate and increased appetite or weight gain.

Be aware of the possible emergence of serious neuropsychiatric symptoms, such as agitation, depressed mood, or changes in behaviour during a quit attempt with or without varenicline, tell your doctor or pharmacist if you experience such symptoms.

Serious side effects of either an uncommon or rare frequency have occurred in people attempting to quit smoking with varenicline: seizure, stroke, heart attack, suicidal thoughts, loss of contact with reality and unable to think or judge clearly (psychosis), changes in thinking or behaviour (such as aggression and abnormal behaviour). There have also been reports of severe skin reactions including Erythema Multiforme (a type of rash) and Stevens-Johnson Syndrome (a serious illness with blistering of the skin, mouth, around the eyes or genitals) and serious allergic reactions including angioedema (swelling of the face, mouth, or throat).

Very common: may affect more than 1 in 10 people

  • inflammation of the nose and throat, abnormal dreams, difficulty sleeping, headache,
  • nausea

Common: may affect up to 1 in 10 people

  • chest infection, inflammation of the sinuses
  • increased weight, decreased appetite, increased appetite
  • sleepiness, dizziness, changes in the way things taste
  • shortness of breath, cough
  • heartburn, vomiting, constipation, diarrhoea, feeling bloated, abdominal pain, toothache, indigestion, flatulence, dry mouth
  • skin rash, itching
  • joint ache, muscle ache, back pain
  • chest pain, tiredness
  • abnormal liver function test

Uncommon: may affect up to 1 in 100 people

  • fungal infection, viral infection
  • feeling of panic, difficulty thinking, restlessness, mood swings, depression, anxiety, hallucinations, changes in sex drive
  • seizure, tremor, feeling sluggish, less sensitive to touch
  • conjunctivitis, eye pain
  • ringing in the ears
  • angina, rapid heart rate, palpitations, increased heart rate
  • increased blood pressure, hot flush
  • inflammation of nose, sinuses and throat, congestion of nose, throat and chest, hoarseness, hay fever, throat irritation, congested sinuses, excess mucous from nose causing cough, runny nose
  • red blood in stools, irritated stomach, change of bowel habit, belching, mouth ulcers, pain in the gums
  • reddening of the skin, acne, increased sweating, night sweats
  • muscle spasms, chest wall pain
  • abnormally frequent urination, urination at night
  • increased menstrual flow
  • chest discomfort, flu like illness, fever, feeling weak or unwell
  • high blood sugar
  • heart attack
  • suicidal thoughts
  • changes in thinking or behaviour (such as aggression)

Rare: may affect up to 1 in 1 000 people

  • excessive thirst
  • feeling unwell or unhappy, slow thinking
  • stroke
  • increased muscle tension, difficulty with speech, difficulty with coordination, reduced sense of taste, altered sleep pattern
  • disturbed vision, eyeball discolouration, dilated pupils, sensitivity to light, short-sightedness, watery eyes
  • irregular heart beat or heart rhythm disturbances
  • throat pain, snoring
  • blood in vomit, abnormal stools, coated tongue
  • stiff joints, rib pain
  • glucose in urine, increased urine volume and frequency
  • vaginal discharge, changes in sexual ability
  • feeling cold, cyst
  • diabetes
  • sleep walking
  • loss of contact with reality and unable to think or judge clearly (psychosis)
  • abnormal behaviour
  • severe skin reactions including erythema multiforme (a type of rash) and Stevens-

    Johnson syndrome (a serious illness with blistering of the skin, mouth, around the eyes or genitals)

  • serious allergic reactions including angioedema (swelling of the face, mouth, or throat)
  • abnormal semen analysis
  • increase of C-reactive protein (a marker of inflammation)
  • decreased blood calcium levels (hypocalcaemia)

Not known: frequency cannot be estimated from the available data

  • temporary loss of consciousness

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 also report side effects directly via the Yellow Card Scheme at: 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.

Varenicline_0.5mg_1mg_28_56_11_14

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LeafletSite Barcode/ DataMatrix41096 miniNo. of colours1Page Count2 of 2
4079100Viatris SAP No.400570195;400570198; 400570199;400570200
3846505122944315/0020
40791001

PL 04569/1889, PL

04569/1887, PL 04569/1888

United Kingdomwith
N/AN/A
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PM04339011GTIN/PCN/A335 x 450 mm10.5 pt
Macleods Pharmaceuticals Ltd (Daman - IN)Keyline/Drawing No.Leaflet 335 x 450 mm
N/A
N/A
V6 APR 2025

5. How to store Varenicline

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 blister and carton 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 medicines you no longer use. These measures will help protect the environment.

6. Contents of the pack and other information

What Varenicline tablets contains

  • The active substances is varenicline tartrate. Each film-coated tablet contains 0.5 mg of varenicline (as tartrate).
  • The active substances is varenicline tartrate. Each film-coated tablet contains 1 mg of varenicline (as tartrate).
  • The other ingredients in the tablet are microcrystalline cellulose, calcium hydrogen phosphate, magnesium stearate, with a film-coating containing HPMC 2910/ hypromellose 6 mPas, hydroxypropyl cellulose and titanium dioxide.

What Varenicline looks like and contents of the pack

Varenicline 0.5 mg film-coated tablets are white to off-white coloured, round shaped, biconvex, film-coated tablets, approximately 6.1 mm in diameter, debossed with “M 33” on one side and plain on other side.

Varenicline 1 mg film-coated tablets are white to off-white coloured, capsule shaped, biconvex, film-coated tablets, approximately 10.2 mm x 5.2 mm in diameter, debossed with “M 34” on one side and plain on other side.

Varenicline 0.5 mg film-coated tablets are available in blister packs containing 28 and 56 film-coated tablets.

Varenicline 1 mg film-coated tablets are available in blister packs containing 28, 56, 112 and 140 film-coated tablets.

Varenicline tablets are available in the following pack presentations:

  • Treatment initiation pack in an outer carton containing:

    • One blister of 11 x 0.5 mg film-coated tablets in an inner carton and one blister of 14 x 1 mg film-coated tablets in an inner carton, or
    • One blister of 11 x 0.5 mg film-coated tablets in an inner carton and three blisters of 14 x 1 mg film-coated tablets in an inner carton, or
    • One blister of 11 x 0.5 mg film-coated tablets in an inner carton and 11 blisters of 14 x 1 mg film-coated tablets in an inner carton.
  • Follow-on (maintenance) blister packs containing:

    • 28 or 56 Varenicline 0.5 mg film-coated tablets, or
    • 28, 56, 112 or 140 Varenicline 1 mg film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Viatris,

Station Close,

Potters Bar,

EN6 1TL,

United Kingdom.

Manufacturer

Mylan Hungary Kft

Mylan utca 1

Komarom

2900

Hungary

Mylan Germany GmbH

Benzstrasse 1

Bad Homburg

61352

Germany

Viatris UK Healthcare Limited

Building 20

Station Close

Potters Bar

EN6 1TL

United Kingdom

This leaflet was last revised in 05/2026.

4079100

PM04342224

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 04569/1888

Last revision stated in the text: May 2026 · 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 Varenicline 1 mg film-coated tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Varenicline
Strength 1 mg
Pharmaceutical form Oral tablet
Varenicline 1 mg film-coated tablets are white to off-white coloured, capsule shaped, biconvex, film-coated tablets, approximately 10.2 mm x 5.2 mm in diameter, debossed with “M 34” on one side and plain on other side.
How is it taken Oral
Excipients Microcrystalline cellulose, Calcium hydrogen phosphate, Magnesium stearate, HPMC 2910/Hypromellose 6 mPas, Hydroxypropyl cellulose, Titanium dioxide
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 2 years
Storage This medicinal product does not require any special storage conditions.
Drug group (ATC) Other nervous system drugs; Drugs used in addictive disorders; Drugs used in nicotine dependence
  1. N Nervous system drugs
    1. N07 Other nervous system drugs
      1. N07B Drugs used in addictive disorders
        1. N07BA Drugs used in nicotine dependence
          1. N07BA03 varenicline
Marketing authorisation PL 04569/1888 (first authorised 5 December 2025)
Marketing authorisation holder Generics (U.K.) Limited T/A Viatris
Codes BNF 04100200

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.