Epivir 150 mg film-coated tablets

Spain
Brand name Epivir 150 mg film-coated tablets
Form tablets, film-coated
Active substance / Dosage
LAMIVUDINE · 150 mg
Prescription type Hospital Diagnosis
Registration number 96015001
Epivir 150 mg film-coated tablets tablets, film-coated

Package leaflet: Information for the user

Introduction

Package leaflet: Information for the user

Epivir 150 mg film-coated tablets

lamivudine

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

  • Keep this leaflet. You may need to read it again.
  • If you have any further questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for you only. Do not give it to anyone else, even if they have the same symptoms as yours, because it may harm them.
  • If you experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.

Contents of the leaflet

  1. What Epivir is and what it is used for
  2. What you need to know before taking Epivir
  3. How to take Epivir
  4. Possible side effects
  5. How to store Epivir
  6. Contents of the pack and other information

1. What Epivir is and what it is used for

Epivir is used in the treatment of HIV (human immunodeficiency virus) infection in adults and children.

The active substance in Epivir is lamivudine. Epivir is a type of medicine known as an antiretroviral. It belongs to a group of medicines called nucleoside reverse transcriptase inhibitors (NRTIs).

Epivir does not completely cure HIV infection; it reduces the amount of virus in the body and keeps it at a low level. It also increases the number of CD4 cells in the blood. CD4 cells are a type of white blood cell that play an important role in helping your body fight infection.

Not everyone responds to treatment with Epivir in the same way. Your doctor will monitor the effectiveness of your treatment.

2. What you need to know before taking Epivir

Do not take Epivir

  • if you are allergic to lamivudine or to any of the other ingredients of this medicine (listed in section 6).

Consult your doctor if you think this applies to you.

Take special care with Epivir

Some people who take Epivir or other combination treatments for HIV infection are at increased risk of developing serious adverse effects. You should be aware that the risk is higher:

  • if you have ever had liver disease, including hepatitis B or C (if you have hepatitis B, do not stop taking Epivir without consulting your doctor, as your condition could worsen)
  • if you are significantly overweight (especially if you are female)
  • if you or your child has kidney disease, your dose may need to be adjusted.

Consult your doctor if any of these situations apply to you. You may need additional tests, including blood tests, while taking this medicine. For more information, see section 4.

Be alert to important symptoms

Some people taking medicines for HIV infection develop other disorders, which may be serious. You need to know which important signs and symptoms to watch for while taking Epivir.

Read the information on “Other possible adverse effects of combination HIV treatment” in section 4 of this leaflet.

Other medicines and Epivir

Tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including herbal medicines and those obtained without a prescription.

Remember to inform your doctor or pharmacist if you start taking a new medicine while on Epivir.

The following medicines should not be used together with Epivir:

  • medicines (usually liquids) containing sorbitol and other polyols (such as xylitol, mannitol, lactitol, or maltitol), if taken regularly
  • other medicines containing lamivudine (used to treat HIV infection or hepatitis B virus infection)
  • emtricitabine (used to treat HIV infection)
  • high doses of cotrimoxazole (a combination of trimethoprim and sulfamethoxazole), an antibiotic
  • cladribine (used to treat hairy cell leukemia).

Tell your doctor if you are being treated with any of these medicines.

Pregnancy

If you are pregnant, become pregnant, or are planning to become pregnant, talk to your doctor about the risks and benefits of taking Epivir for both you and your baby.

Epivir and similar medicines may cause adverse effects in babies during pregnancy.

If you have taken Epivir during pregnancy, your doctor may recommend periodic blood tests and other diagnostic tests to monitor your child's development. In children whose mothers took NRTIs during pregnancy, the benefit of protection against HIV was greater than the risk of adverse effects occurring.

Breast-feeding

Breast-feeding is not recommended for women living with HIV because HIV infection can be transmitted to the baby through breast milk.

A small amount of the components of Epivir may also pass into breast milk.

If you are breast-feeding or considering breast-feeding, you should consult your doctor as soon as possible.

Driving and using machines

It is unlikely that Epivir will affect your ability to drive or use machines.

Epivir contains sodium

This medicine contains less than 1 mmol of sodium (23 mg) per dose unit; that is, essentially “sodium-free”.

3. How to take Epivir

Follow exactly the instructions for using this medicine given by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

Swallow the Epivir tablets with a little water. Epivir may be taken with or without food.

If you cannot swallow the tablets whole, you may break them and mix them with a small amount of food or drink; take the entire dose immediately.

Keep regular contact with your doctor

Epivir helps control your condition. You will need to take it every day to prevent your condition from worsening. You may develop other infections and illnesses associated with HIV infection.

Stay in contact with your doctor and do not stop taking Epivir without first talking to your doctor.

How much to take

Adults, adolescents, and children weighing at least 25 kg:

The usual dose of Epivir is 300 mg daily. This may be taken as one 150 mg tablet twice daily (approximately 12 hours apart), or as two 150 mg tablets once daily, as directed by your doctor.

Children weighing at least 20 kg but less than 25 kg:

The usual dose of Epivir is 225 mg daily. This may be given as 75 mg (half a 150 mg tablet) in the morning and 150 mg (one whole tablet) in the evening, or as 225 mg (one and a half 150 mg tablets) once daily, as directed by your doctor.

Children weighing at least 14 kg but less than 20 kg:

The usual dose of Epivir is 150 mg daily. This may be taken as 75 mg (half a 150 mg tablet) twice daily (approximately 12 hours apart), or as 150 mg (one 150 mg tablet) once daily, as directed by your doctor.

Epivir is also available as an oral solution for the treatment of children over three months of age and for patients who cannot swallow tablets or who require a lower than usual dose.

If you or your child has a kidney problem, your dose may need to be adjusted.

Consult your doctor if this applies to you or your child.

If you take more Epivir than you should

If you take more Epivir than you should, inform your doctor or pharmacist, or contact the nearest hospital emergency department for further advice. If possible, show them the Epivir packaging.

If you forget to take Epivir

If you forget to take a dose, take it as soon as you remember, then continue with your regular dosing schedule.

Do not take a double dose to make up for forgotten doses.

4. Possible adverse effects

During HIV treatment, there may be an increase in weight and in blood glucose and lipid levels. This may be partly related to the recovery of health and lifestyle, and in the case of blood lipids, sometimes to the HIV medicines themselves. Your doctor will monitor you for these changes.

Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.

When undergoing HIV treatment, it may be difficult to determine whether a symptom is an adverse effect of Epivir or of other medicines you are taking, or whether it is due to the HIV disease itself. Therefore, it is very important that you inform your doctor about any changes in your health.

In addition to the adverse effects listed below for Epivir, other disorders may develop during combination HIV treatment.

It is important that you read the information under the section "Other possible adverse effects of combination HIV treatment."

Frequent adverse effects

May affect up to 1 in 10 people:

  • headache
  • discomfort (nausea)
  • vomiting
  • diarrhea
  • stomach pain
  • fatigue, lack of energy
  • fever (high temperature)
  • general feeling of being unwell
  • muscle pain and discomfort
  • joint pain
  • difficulty sleeping (insomnia)
  • cough
  • irritated nose or excessive nasal discharge
  • skin rash
  • hair loss (alopecia).

Uncommon adverse effects

May affect up to 1 in 100 people:

Uncommon adverse effects that may appear in blood tests include:

  • a decrease in the number of cells involved in blood clotting (thrombocytopenia)
  • low red blood cell count (anemia) or low white blood cell count (neutropenia)
  • increased levels of liver-produced enzymes.

Rare adverse effects

May affect up to 1 in 1,000 people:

  • severe allergic reaction causing swelling of the face, tongue, or throat, which may cause difficulty swallowing or breathing
  • inflammation of the pancreas (pancreatitis)
  • muscle tissue breakdown
  • inflammation (hepatitis).

A rare adverse effect that may appear in blood tests is:

  • increase in an enzyme called amylase.

Very rare adverse effects

May affect up to 1 in 10,000 people:

  • lactic acidosis (excess lactic acid in the blood)
  • tingling or numbness in the arms, legs, hands, or feet.

A very rare adverse effect that may appear in blood tests is:

  • failure of the bone marrow to produce new red blood cells (pure red cell aplasia).

If you experience adverse effects

Inform your doctor or pharmacist if you consider any of the adverse effects you experience to be severe, or if you notice any adverse effects not listed in this leaflet.

Other possible adverse effects of combination HIV treatment

Combination treatments, such as Epivir, may cause other disorders to develop during HIV treatment.

Exacerbation of previous infections

People with advanced HIV infection (AIDS) have weakened immune systems and are more likely to develop serious infections (opportunistic infections). When these people start treatment, they may find that previous, hidden infections flare up again, causing signs and symptoms of inflammation. These symptoms are likely due to an improved immune response, which enables the body to fight these infections.

In addition to these opportunistic infections, autoimmune disorders (a condition in which the immune system attacks healthy body tissue) may also occur after you have started taking medicines for your HIV infection. Autoimmune disorders may occur many months after starting treatment. If you notice any symptoms of infection or other symptoms such as muscle weakness, weakness in the hands and feet spreading toward the trunk, palpitations, tremors, or hyperactivity, please inform your doctor immediately to receive the necessary treatment.

If you notice any symptoms of infection while taking Epivir:

Inform your doctor immediately. Do not take any other medicine for the infection unless advised by your doctor.

You may have problems with your bones

Some people receiving combination HIV treatment may develop a bone disease called osteonecrosis. In this disease, part of the bone tissue dies due to reduced blood supply to the bone. People are more likely to develop this condition:

  • if they have been on combination treatment for a long time
  • if they also take anti-inflammatory medicines called corticosteroids
  • if they drink alcohol
  • if their immune system is severely weakened
  • if they are overweight.

Signs of osteonecrosis include:

  • joint stiffness
  • pain and discomfort (especially in the hip, knee, or shoulder)
  • difficulty moving.

If you notice any of these symptoms:

Inform your doctor.

Reporting of adverse effects

If you experience any type of adverse effect, consult your doctor or pharmacist, even if they are possible adverse effects not listed in this leaflet. You can also report them directly through the national reporting system detailed in Appendix V. By reporting adverse effects, you can help provide more information on the safety of this medicine.

5. Storage of Epivir

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

Do not use this medicine after the expiry date stated on the carton.

Do not store Epivir above 30 °C.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines and containers you no longer need. This will help protect the environment.

6. Contents of the pack and other information

Composition of Epivir

The active substance is lamivudine.

The other components are:

  • Tablet core: microcrystalline cellulose, sodium carboxymethyl starch (gluten-free), magnesium stearate
    • Film coating: hypromellose, titanium dioxide, macrogol, and polysorbate 80.

Appearance of Epivir and contents of the pack

Epivir 150 mg film-coated tablets are supplied in white polyethylene bottles or blisters containing 60 tablets. The tablets are white, scored, diamond-shaped, and engraved with the code “GXCJ7” on both sides.

Marketing Authorization Holder and Manufacturer

Manufacturer

Marketing Authorization Holder

Delpharm Poznan Spólka Akcyjna

ul. Grunwaldzka 189

60-322 Poznan

Poland

ViiV Healthcare BV

Van Asch van Wijckstraat 55H

3811 LP Amersfoort

Netherlands

You can request further information about this medicinal product by contacting the local representative of the marketing authorization holder:

Belgium/Belgium/Belgium

ViiV Healthcare srl/bv

Tel/Tel: + 32 (0)10 85 65 00

Lithuania

ViiV Healthcare BV

Tel: + 370 80000334

Bulgaria

ViiV Healthcare BV

Tel: + 359 80018205

Luxembourg/Luxembourg

ViiV Healthcare srl/bv

Belgium/Belgium

Tel/Tel: + 32 (0)10 85 65 00

Czech Republic

GlaxoSmithKline s.r.o.

Tel: + 420 222 001 111

[email protected]

Hungary

ViiV Healthcare BV

Tel.: + 36 80088309

Denmark

GlaxoSmithKline Pharma A/S

Tlf: + 45 36 35 91 00

[email protected]

Malta

ViiV Healthcare BV

Tel: + 356 80065004

Germany

ViiV Healthcare GmbH

Tel.: + 49 (0)89 203 0038-10

[email protected]

Netherlands

ViiV Healthcare BV

Tel: + 31 (0) 33 2081199

Estonia

ViiV Healthcare BV

Tel: + 372 8002640

[email protected]

Norway

GlaxoSmithKline AS

Tlf: + 47 22 70 20 00

Greece

GlaxoSmithKline Monoypoxei A.E.B.E.

Tel: + 30 210 68 82 100

Austria

GlaxoSmithKline Pharma GmbH

Tel: + 43 (0)1 97075 0

[email protected]

Spain

Laboratorios ViiV Healthcare, S.L.

Tel: + 34 900 923 501

[email protected]

Poland

GSK Services Sp. z o.o.

Tel.: + 48 (0)22 576 9000

France

ViiV Healthcare SAS

Tél.: + 33 (0)1 39 17 6969

[email protected]

Portugal

VIIVHIV HEALTHCARE, UNIPESSOAL, LDA.

Tel: + 351 21 094 08 01

[email protected]

Croatia

ViiV Healthcare BV

Tel: +385 800787089

Romania

ViiV Healthcare BV

Tel: + 40 800672524

Ireland

GlaxoSmithKline (Ireland) Limited

Tel: + 353 (0)1 4955000

Slovenia

ViiV Healthcare BV

Tel: + 386 80688869

Iceland

Vistor hf.

Tel: +354 535 7000

Slovakia

ViiV Healthcare BV

Tel: + 421 800500589

Italy

ViiV Healthcare S.r.l.

Tel: + 39 (0)45 7741600

Finland

GlaxoSmithKline Oy

Tel/Tel: + 358 (0)10 30 30 30

Cyprus

ViiV Healthcare BV

Tel: + 357 80070017

Sweden

GlaxoSmithKline AB

Tel: + 46 (0)8 638 93 00

[email protected]

Latvia

ViiV Healthcare BV

Tel: + 371 80205045

United Kingdom (Northern Ireland)

ViiV Healthcare BV Limited

Tel: + 44 (0)800 221441

[email protected]

Date of the most recent review of this summary: {MM/YYYY}.

Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu