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Entecavir Sun 0.5 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:
0.5 mg
Contains active substance:
ATC code:

Patient leaflet - Entecavir Sun 0.5 mg film-coated tablets

1. What Entecavir is and what it is used for

Entecavir tablets are anti-viral medicines, used to treat chronic (long term) hepatitis B virus (HBV) infection in adults. Entecavir can be used in people whose liver is damaged but still functions properly (compensated liver disease) and in people whose liver is damaged and does not function properly (decompensated liver disease).

Entecavir tablets are also used to treat chronic (long term) HBV infection in children and adolescents aged 2 years to less than 18 years. Entecavir can be used in children whose liver is damaged but still functions properly (compensated liver disease).

Infection by the hepatitis B virus can lead to damage to the liver. Entecavir reduces the amount of virus in your body, and improves the condition of the liver.

2. What you need to know before you take Entecavir

Do not take Entecavir if you are allergic to entecavir or any of the other ingredients of this medicine (listed in section 6).

Warning and precautions

Talk to your doctor or pharmacist before taking Entecavir

  • if you have ever had problems with your

    kidneys, tell your doctor. This is important because Entecavir is eliminated from your body through the kidneys and your dose or dosing schedule may need to be adjusted.

  • do not stop taking Entecavir without your

    doctor's advice since your hepatitis may worsen after stopping treatment. When your treatment with Entecavir is stopped, your doctor will continue to monitor you and take blood tests for several months.

  • discuss with your doctor whether your liver

    functions properly and, if not, what the possible effects on your Entecavir treatment may be.

  • if you are also infected with HIV (human

    immunodeficiency virus) be sure to tell your doctor. You should not take Entecavir to treat your hepatitis B infection unless you are taking medicines for HIV at the same time, as the effectiveness of future HIV treatment may be reduced. Entecavir will not control your HIV infection.

  • taking Entecavir will not stop you from infecting

    other people with hepatitis B virus (HBV) through sexual contact or body fluids (including blood contamination). So, it is important to take appropriate precautions to prevent others from becoming infected with HBV. A vaccine is available to protect those at risk from becoming infected with HBV.

  • Entecavir belongs to a class of medicines that

    can cause lactic acidosis (excess of lactic acid in your blood) and enlargement of the liver. Symptoms such as nausea, vomiting and stomach pain might indicate the development of lactic acidosis. This rare but serious side effect has occasionally been fatal. Lactic acidosis occurs more often in women, particularly if they are very overweight. Your doctor will monitor you regularly while you are receiving Entecavir.

    • if you have previously received treatment for

      chronic hepatitis B, please inform your doctor.

Children and adolescents

Entecavir should not be used for children below 2 years of age or weighing less than 10 kg.

Other medicines and Entecavir

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

Entecavir with food and drink

In most cases you may take Entecavir with or without food. However, if you have had a previous treatment with a medicine containing the active substance lamivudine you should consider the following: If you were switched over to Entecavir because the treatment with lamivudine was not successful, you should take Entecavir on an empty stomach once daily. If your liver disease is very advanced, your doctor will also instruct you to take Entecavir on an empty stomach. Empty stomach means at least 2 hours after a meal and at least 2 hours before your next meal.

Children and adolescents (from 2 to less than 18 years of age) can take Entecavir with or without food.

Pregnancy, breast-feeding and fertility

Tell your doctor if you are pregnant or planning to become pregnant. It has not been demonstrated that Entecavir is safe to use during pregnancy. Entecavir must not be used during pregnancy unless specifically directed by your doctor. It is important that women of childbearing age receiving treatment with Entecavir use an effective method of contraception to avoid becoming pregnant.

You should not breast-feed during treatment with Entecavir. Tell your doctor if you are breastfeeding. It is not known whether entecavir, the active ingredient in Entecavir, is excreted in human breast milk.

Driving and using machines

Dizziness, tiredness (fatigue) and sleepiness (somnolence) are common side effects which may impair your ability to drive and use machines. If you have any concerns consult your doctor.

Entecavir contains lactose

This medicinal product 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.

3. How to take Entecavir

Not all patients need to take the same dose of Entecavir.

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

For adults the recommended dose is either 0.5 mg or 1 mg once daily orally (by mouth).

Your dose will depend on:

  • whether you have been treated for HBV infection

    before, and what medicine you received.

  • whether you have kidney problems. Your doctor

    may prescribe a lower dose for you or instruct you to take it less often than once a day.

  • the condition of your liver.

For children and adolescents (from 2 to less than 18 years of age) your child's doctor will decide the right dose based on your child's weight.

An entecavir oral solution is recommended for patients weighing from 10 kg to 32.5 kg. Children weighing at least 32.6 kg may take an entecavir oral solution or the 0.5 mg tablet or may be available. All dosing will be taken once daily orally (by mouth). There are no recommendations for entecavir in children less than 2 years of age or weighing less than 10 kg.

Your doctor will advise you on the dose that is right for you. Always take the dose recommended by your doctor to ensure that your medicine is fully effective and to reduce the development of resistance to treatment. Take Entecavir for as long as your doctor has told you. Your doctor will tell you if and when you should stop the treatment.

Some patients must take Entecavir on an empty stomach (see Entecavir with food and drink in Section 2). If your doctor instructs you to take Entecavir on an empty stomach, empty stomach means at least 2 hours after a meal and at least 2 hours before your next meal.

If you take more Entecavir than you should

Contact your doctor at once.

If you forget to take Entecavir

It is important that you do not miss any doses. If you miss a dose of Entecavir, take it as soon as possible, and then take your next scheduled dose at its regular time. If it is almost time for your next dose, do not take the missed dose. Wait and take the next dose at the regular time. Do not take a double dose to make up for a forgotten dose.

Do not stop Entecavir without your doctor's advice

Some people get very serious hepatitis symptoms when they stop taking Entecavir. Tell your doctor immediately about any changes in symptoms that you notice after stopping treatment.

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.

Patients treated with entecavir have reported the following side effects:

Entecavir can cause a rare but serious side effect called lactic acidosis (excess of lactic acid in your blood) and enlargement of the liver. Please see Section 2 under Warnings and Precautions for more information.

Adults

Common (at least 1 in 100 patients):

  • headache
  • insomnia (inability to sleep), somnolence

    (sleepiness)

  • fatigue (extreme tiredness)
  • dizziness
  • vomiting, diarrhoea, nausea, dyspepsia

    (indigestion)

  • increased blood levels of liver enzymes

Uncommon (at least 1 in 1,000 patients):

  • rash
  • hair loss

Rare (at least 1 in 10,000 patients):

  • severe allergic reaction

Children and adolescents

The side effects experienced in children and adolescents are similar to those experienced in adults as described above with the following difference: Very common (at least 1 in 10 patients): low levels of neutrophils (one type of white blood cells, which are important in fighting infection).

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 Entecavir

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 label and carton after EXP.

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

This medicinal product does not require any special storage conditions.

Bottle: Use within 30 days after the first opening of the bottle.

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 Entecavir contains

  • The active substance is entecavir.
  • Entecavir 0.5 mg: Each film-coated tablet contains

    0.5 mg entecavir.

    • Entecavir 1 mg: Each film-coated tablet contains 1 mg entecavir.
    • The other ingredients are:

      Tablet core: Lactose Monohydrate, Povidone K30, Crospovidone, Microcrystalline cellulose PH 102 and Magnesium stearate.

      Film coating:

      0.5 mg: Opadry 13B58802 White (containing HPMC 2910/Hypromellose (E464), Titanium dioxide (E171), Macrogol 400 (E1521) and Polysorbate 80 (E433)). 1 mg: Opadry 13B84610 Pink (containing HPMC 2910/Hypromellose (E464), Titanium dioxide (E171), Macrogol 400 (E1521), Polysorbate 80 (E433) and iron oxide (red) (E172)).

What Entecavir looks like and contents of the pack

Entecavir 0.5 mg film-coated tablets are white to off white, triangular shaped film coated tablets, of dimensions 8.60 X 8.30 mm, debossed with 'RL1' on one side and plain on other side.

Entecavir 1 mg film-coated tablets are light pink to pink, triangular shaped film-coated tablets, of dimensions 10.90 X 10.60 mm, debossed with 'RL2' on one side and plain on other side.

The film-coated tablets are available in HDPE bottle, in blister packs containing 30 or 90 film-coated tablets and in unit dose blister packs containing 30 x 1 or 90 x 1 film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87

2132 JH Hoofddorp

The Netherlands

Manufacturer(s)

S.C. Terapia S.A.

Str. Fabricii nr. 124,

400 632 Cluj Napoca

Romania

Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87

2132 JH Hoofddorp

The Netherlands

Alkaloida Chemical Company Zrt

Kabay János u.29, Tiszavasvári, H-4440,

Hungary

This medicinal product is authorised in the Member States of the EEA under the following names:

Germany: ENTECAVIR BASICS 0.5 mg,

Filmtabletten

ENTECAVIR BASICS 1 mg,

Filmtabletten

Italy: Entecavir SUN 0.5 mg compresse rivestite con film

Entecavir SUN 1 mg compresse rivestite con film

Poland: Entecavir Ranbaxy

Romania: Entecavir Terapia 0.5 mg comprimate filmate

Entecavir Terapia 1 mg comprimate filmate

Spain: Entecavir SUN 0.5 mg comprimidos recubiertos con película EFG Entevavir SUN 1 mg comprimidos recubiertos con película EFG United Kingdom: Entecavir 0.5 mg film coated tablets

Entecavir 1 mg film coated tablets

This leaflet was last revised in February 2023.

Entecavir 0.5 mg film-coated tablets

Entecavir 1 mg

film-coated tablets

Entecavir

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 31750/0107

Last revision stated in the text: February 2023 · 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 Entecavir Sun 0.5 mg film-coated tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Entecavir
Strength 0.5 mg
Pharmaceutical form Oral tablet
White to off white and triangular-shaped, of dimensions 8.60 X 8.30 mm, debossed with “RL1” on one side and plain on the other side.
How is it taken Oral
Excipients Lactose Monohydrate (Pharmatose 200M), Povidone K30, Crospovidone, Microcrystalline Cellulose PH 102, Magnesium stearate, HPMC 2910/Hypromellose (E464), Titanium dioxide (E171), Macrogol 400 (E1521), Polysorbate 80 (E433)
Pack sizes 30 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life Shelf life: 2 years
Shelf life after opening: 30 days
Storage This medicinal product does not require any special storage conditions.
Drug group (ATC) Antivirals for systemic use, nucleoside and nucleotide reverse transcriptase inhibitors
  1. J Antiinfectives for systemic use
    1. J05 Antivirals for systemic use
      1. J05A Direct acting antivirals
        1. J05AF Nucleoside and nucleotide reverse transcriptase inhibitors
          1. J05AF10 entecavir
Marketing authorisation PL 31750/0107 (first authorised 4 October 2018)
Marketing authorisation holder Sun Pharmaceutical Industries Europe B.V.
Codes GTIN 8718531948310 · BNF 05030301

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.