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Amlodipine/Valsartan 5 mg/160 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:
5 mg / 160 mg
Contains active substances:

Patient leaflet - Amlodipine/valsartan 5 mg / 160 mg film-coated tablets

1. What Amlodipine/Valsartan is and what it is used for

Amlodipine/Valsartan tablets contain two substances called amlodipine and valsartan. Both of these substances help to control high blood pressure.

  • Amlodipine belongs to a group of substances called “calcium channel blockers”. Amlodipine stops calcium from moving into the blood vessel wall which stops the blood vessels from tightening.
  • Valsartan belongs to a group of substances called “angiotensin-II receptor antagonists”.

    Angiotensin II is produced by the body and makes the blood vessels tighten, thus increasing the blood pressure. Valsartan works by blocking the effect of angiotensin II. This means that both of these substances help to stop the blood vessels tightening. As a result, the blood vessels relax and blood pressure is lowered.

Amlodipine/Valsartan is used to treat high blood pressure in adults whose blood pressure is not controlled enough with either amlodipine or valsartan on its own.

2. What you need to know before you take Amlodipine/Valsartan

DO NOT take Amlodipine/Valsartan

  • if you are allergic to amlodipine or to any other calcium channel blockers. This may involve itching, reddening of the skin or difficulty in breathing
  • if you are allergic to valsartan or any of the other ingredients of this medicine (listed in section 6). If you think you may be allergic, talk to your doctor before taking Amlodipine/Valsartan
  • if you have severe liver problems or bile problems such as biliary cirrhosis or cholestasis
  • if you are more than 3 months pregnant. (It is also better to avoid Amlodipine/Valsartan in early pregnancy, see Pregnancy section)
  • if you have severe low blood pressure (hypotension)
  • if you have narrowing of the aortic valve (aortic stenosis) or cardiogenic shock (a condition where your heart is unable to supply enough blood to the body)

    if you suffer from heart failure after a heart attack

  • if you have diabetes or impaired kidney function and you are treated with a blood pressure lowering medicine containing aliskiren

If any of the above applies to you, do not take Amlodipine/Valsartan and talk to your doctor.

Warnings and precautions

Talk to your doctor before taking Amlodipine/Valsartan:

  • if you have been sick (vomiting or diarrhoea)
  • if you have liver or kidney problems
  • if you have had a kidney transplant or if you had been told that you have a narrowing of your kidney arteries
  • if you have a condition affecting the renal glands called “primary hyperaldosteronism”
  • if you have had heart failure or have experienced a heart attack. Follow your doctor’s instructions for the starting dose carefully. Your doctor may also check your kidney function
  • if your doctor has told you that you have a narrowing of the valves in your heart (called

    “aortic or mitral stenosis”) or that the thickness of your heart muscle is abnormally increased (called “obstructive hypertrophic cardiomyopathy”)

  • if you have experienced swelling, particularly of the face and throat, while taking other medicines (including angiotensin converting enzyme inhibitors). If you get these symptoms, stop taking Amlodipine/Valsartan and contact your doctor straight away. You should never take Amlodipine/Valsartan again
  • if you are taking any of the following medicines used to treat high blood pressure: o an

    ACE inhibitor (for example enalapril, lisinopril, ramipril), in particular if you have diabetes-related kidney problems

    • aliskiren

Your doctor may check your kidney function, blood pressure, and the amount of electrolytes (e.g. potassium) in your blood at regular intervals.

See also information under the heading “DO NOT take Amlodipine/Valsartan”.

If any of these apply to you, tell your doctor before taking Amlodipine/Valsartan.

Talk to your doctor if you experience abdominal pain, nausea, vomiting or diarrhoea after taking Amlodipine/Valsartan. Your doctor will decide on further treatment. Do not stop taking Amlodipine/Valsartan on your own.

Children and adolescents

The use of Amlodipine/Valsartan in children and adolescents is not recommended (aged below 18 years old).

Other medicines and Amlodipine/Valsartan

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Your doctor may need to change your dose and/or to take other precautions. In some cases you may have to stop taking one of the medicines. This applies especially to the medicines listed below:

  • ACE inhibitors or aliskiren (see also information under the headings “DO NOT take

    Amlodipine/Valsartan” and “Warnings and precautions”)

  • diuretics (a type of medicine also called “water tablets” which increases the amount of urine you produce)
  • lithium (a medicine used to treat some types of depression)
  • potassium-sparing diuretics, potassium supplements, salt substitutes containing potassium and other substances that may increase potassium levels
  • certain types of painkillers called non-steroidal anti-inflammatory medicines (NSAIDs) or selective cyclooxygenase-2 inhibitors (COX-2 inhibitors). Your doctor may also check your kidney function

    anticonvulsant agents (e.g. carbamazepine, phenobarbital, phenytoin, fosphenytoin, primidone)

  • St. John’s wort
  • nitroglycerin and other nitrates, or other substances called “vasodilators”
  • medicines used for HIV/AIDS (e.g. ritonavir, indinavir, nelfinavir)
  • medicines used to treat fungal infections (e.g. ketoconazole, itraconazole)
  • medicines used to treat bacterial infections (antibiotics - such as rifampicin, erythromycin, clarithromycin, telithromycin)
  • verapamil, diltiazem (heart medicines)
  • simvastatin (a medicine used to control high cholesterol levels)
  • dantrolene (infusion for severe body temperature abnormalities)
  • medicines used to protect against transplant rejection (ciclosporin)

Amlodipine/Valsartan with food and drink

Grapefruit and grapefruit juice should not be consumed by people who are taking Amlodipine/Valsartan. This is because grapefruit and grapefruit juice can lead to an increase in the blood levels of the active substance amlodipine, which can cause an unpredictable increase in the blood pressure lowering effect of Amlodipine/Valsartan.

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 for advice before taking this medicine.

Pregnancy

You must tell your doctor if you think you are (or might become) pregnant. Your doctor will normally advise you to stop taking Amlodipine/Valsartan before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine instead of Amlodipine/Valsartan. Amlodipine/Valsartan is not recommended in early pregnancy (first 3 months), and must not be taken when more than 3 months pregnant, as it may cause serious harm to your baby if used after the third month of pregnancy.

Breast-feeding

Amlodipine, one of the two active ingredients of Amlodipine/Valsartan, has been shown to pass into breast milk in small amounts. Tell your doctor if you are breast-feeding or about to start breast-feeding. Amlodipine/Valsartan is not recommended for mothers who are breastfeeding, and your doctor may choose another treatment for you if you wish to breast-feed, especially if your baby is newborn, or was born prematurely.

Driving and using machines

This medicine may make you feel dizzy. This can affect how well you can concentrate. So, if you are not sure how this medicine will affect you do not drive, use machinery, or do other activities that you need to concentrate on.

Amlodipine/Valsartan 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 Amlodipine/Valsartan

Always take this medicine exactly as your doctor has told you. Check with your doctor if you are not sure. This will help you get the best results and lower the risk of side effects.

The recommended dose of Amlodipine/Valsartan is one tablet per day. It is preferable to take your medicine at the same time each day. Swallow the tablets with a glass of water.

You can take Amlodipine/Valsartan with or without food. Do not take Amlodipine/Valsartan with grapefruit or grapefruit juice.

Depending on how you respond to the treatment, your doctor may suggest a higher or lower dose.

Do not exceed the prescribed dose.

Amlodipine/Valsartan and elderly (age 65 years or over)

Your doctor should exercise caution when increasing your dose.

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

If you take more Amlodipine/Valsartan than you should

If you have taken too many tablets of Amlodipine/Valsartan, or if someone else has taken your tablets, consult a doctor immediately.

Excess fluid may accumulate in your lungs (pulmonary oedema) causing shortness of breath that may develop up to 24-48 hours after intake.

If you forget to take Amlodipine/Valsartan

If you forget to take this medicine, take it as soon as you remember. Then take your next dose at its usual time. However, if it is almost time for your next dose, skip the dose you missed. Do not take a double dose to make up for a forgotten tablet.

If you stop taking Amlodipine/Valsartan

Stopping your treatment with Amlodipine/Valsartan may cause your disease to get worse. Do not stop taking your medicine unless your doctor tells you to.

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.

Some side effects can be serious and need immediate medical attention: A few patients have experienced these serious side effects (may affect up to 1 in 1,000 people). If any of the following happen, tell your doctor straight away:

Allergic reaction with symptoms such as rash, itching, swelling of face or lips or tongue, difficulty breathing, low blood pressure (feeling of faintness, light-headedness). Other possible side effects of Amlodipine/Valsartan

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

  • influenza (flu)
  • blocked nose, sore throat and discomfort when swallowing
  • headache
  • swelling of arms, hands, legs, ankles or feet
  • tiredness
  • asthenia (weakness)
  • redness and warm feeling of the face and/or neck

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

  • dizziness
  • nausea and abdominal pain
  • dry mouth
  • drowsiness, tingling or numbness of the hands or feet
  • vertigo
  • fast heartbeat including palpitations

    dizziness on standing up

  • cough
  • diarrhoea
  • constipation
  • skin rash, redness of the skin
  • joint swelling, back pain pain in joints

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

  • feeling anxious
  • ringing in the ears (tinnitus)
  • fainting
  • passing more urine than normal or feeling more of an urge to pass urine
  • inability to get or maintain an erection
  • sensation of heaviness
  • low blood pressure with symptoms such as dizziness, light-headedness
  • excessive sweating
  • skin rash all over your body; itching; muscle spasm

If any of these affect you severely, tell your doctor.

Side effects reported with amlodipine or valsartan alone and either not observed with Amlodipine/Valsartan or observed with a higher frequency than with Amlodipine/Valsartan:

Amlodipine

Consult a doctor immediately if you experience any of the following very rare, severe side effects after taking this medicine:

  • sudden wheeziness, chest pain, shortness of breath or difficulty in breathing
  • swelling of eyelids, face or lips
  • swelling of the tongue and throat which causes great difficulty breathing
  • severe skin reactions including intense skin rash, hives, reddening of the skin over your whole body, severe itching, blistering, peeling and swelling of the skin, inflammation of the mucous membranes (Stevens-Johnson Syndrome, toxic epidermal necrolysis) or other allergic reactions
  • heart attack, abnormal heartbeat
  • inflamed pancreas, which may cause severe abdominal and back pain accompanied with feeling of being very unwell

The following side effects have been reported. If any of these cause you problems or if they last for more than one week, you should contact your doctor.

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

  • dizziness, sleepiness
  • palpitations (awareness of your heartbeat)
  • flushing, ankle swelling (oedema)
  • abdominal pain, feeling sick (nausea)

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

  • mood changes, anxiety, depression, sleeplessness, trembling, taste abnormalities, fainting, loss of pain sensation
  • visual disturbances, visual impairment, ringing in the ears
  • low blood pressure
  • sneezing/runny nose caused by inflammation of the lining of the nose (rhinitis) indigestion,

    vomiting (being sick)

    hair loss, increased sweating, itchy skin, skin discolouration

  • disorder in passing urine, increased need to urinate at night, increased number of times of passing urine
  • inability to obtain an erection, discomfort or enlargement of the breasts in men, pain, feeling unwell, muscle pain, muscle cramps; weight increase or decrease

Rare (may affect up to 1 in 1,000 people): confusion

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

  • decreased number of white blood cells, decrease in blood platelets which may result in unusual bruising or easy bleeding (red blood cell damage)
  • excess sugar in blood (hyperglycaemia)
  • swelling of the gums, abdominal bloating (gastritis)
  • abnormal liver function, inflammation of the liver (hepatitis), yellowing of the skin

    (jaundice), liver enzyme increase which may have an effect on some medical tests

  • increased muscle tension
  • inflammation of blood vessels often with skin rash, sensitivity to light; disorders combining rigidity, tremor and/or movement disorders

Valsartan

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

  • intestinal angioedema: a swelling in the gut presenting with symptoms like abdominal pain, nausea, vomiting and diarrhoea

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

  • decrease in red blood cells, fever, sore throat or mouth sores due to infections
  • spontaneous bleeding or bruising
  • high level of potassium in the blood
  • abnormal liver test results
  • decreased renal functions and severely decreased renal functions
  • swelling mainly of the face and the throat
  • muscle pain
  • rash, purplish-red spots
  • fever
  • itching
  • allergic reaction, blistering skin (sign of a condition called dermatitis bullous)

If you experience any of these, tell your doctor straight away.

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.

5. How to store Amlodipine/Valsartan

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 box and on the blister strip (“EXP or country-specific”). The expiry date refers to the last day of that month.

Do not store above 30 °C. Store in the original container in order to protect from moisture.

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 Amlodipine/Valsartan contains

The active substances of Amlodipine/Valsartan are amlodipine (as amlodipine besilate) and valsartan.

Amlodipine/Valsartan 5mg/80mg film-coated tablets

Each film-coated tablet contains 5 mg amlodipine (as amlodipine besilate) and 80 mg valsartan.

Amlodipine/Valsartan 5mg/160mg film-coated tablets

Each film-coated tablet contains 5 mg amlodipine (as amlodipine besilate) and 160 mg valsartan.

Amlodipine/Valsartan 10mg/160mg film-coated tablets

Each film-coated tablet contains 10 mg amlodipine (as amlodipine besilate) and 160 mg valsartan.

The other ingredients are:

Tablet core:

cellulose microcrystalline; povidone; starch, pregelatinised (Maize); silica colloidal anhydrous, crospovidone; sodium starch glycolate; magnesium stearate

Film-coat:

Amlodipine/Valsartan 5mg/80mg film-coated tablets

hypromellose; titanium dioxide (E171); iron oxide yellow (E172); talc; macrogol; iron oxide black (E172)

Amlodipine/Valsartan 5mg/160mg film-coated tablets

hypromellose; titanium dioxide (E171); iron oxide yellow (E172); talc; macrogol; iron oxide black (E172)

Amlodipine/Valsartan 10mg/160mg film-coated tablets hypromellose; titanium dioxide (E171); iron oxide yellow (E172); talc; macrogol

What Amlodipine/Valsartan looks like and contents of the pack

Amlodipine/Valsartan 5 mg/80 mg film-coated tablets are dark yellow, round, biconvex filmcoated tablets.

Amlodipine/Valsartan 5 mg/160 mg film-coated tablets are dark yellow, oval, biconvex filmcoated tablets.

Amlodipine/Valsartan 10 mg/160 mg film-coated tablets are pale yellow, oval, biconvex filmcoated tablets.

The film-coated tablets are available in blister packs of 7, 10,

14, 28, 30, 56, 60, 84, 90, 98, 100 film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

STADA

Linthwaite, Huddersfield, HD7 5QH, UK

Manufacturer

STADA Azneimittel AG,

Stadastrasse 2-18,

61118 Bad Vilbel,

Germany

This leaflet was last revised in July 2025

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 06831/0316

Last revision stated in the text: July 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 Amlodipine/valsartan 5 mg / 160 mg film-coated tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substances Amlodipine, Valsartan
Strength 5 mg / 160 mg
Pharmaceutical form Oral tablet
Dark yellow, oval, biconvex film-coated tablets with length of 14.6 ± 0.2 mm and width 6.8 ± 0.2 mm
How is it taken Oral
Excipients Cellulose microcrystalline, Povidone, Starch, pregelatinised (Maize), Silica colloidal anhydrous, Crospovidone, Sodium starch glycolate, Magnesium stearate, Hypromellose, Titanium dioxide (E171), Iron oxide yellow (E172), Talc, Macrogol, Iron oxide black (E172)
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years
Storage Do not store above 30 °C. Store in the original container in order to protect from moisture.
Drug group (ATC) Agents acting on the renin-angiotensin system; angiotensin II antagonists, combinations; angiotensin II antagonists and calcium channel blockers
  1. C Cardiovascular system drugs
    1. C09 Agents acting on the renin-angiotensin system
      1. C09D Angiotensin II receptor blockers (ARBs), combinations
        1. C09DB Angiotensin II receptor blockers (ARBs) and calcium channel blockers
          1. C09DB01 valsartan and amlodipine
Marketing authorisation PL 06831/0316 (first authorised 20 February 2025)
Marketing authorisation holder Genus Pharmaceuticals Ltd. (trading as ‘STADA’)
Codes BNF 02060200

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.1.0 of 12 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.