Epivir

lamivudine

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This is a summary of the European Public Assessment Report (EPAR) for Epivir. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Epivir.

What is Epivir?

Epivir is a medicine containing the active substance lamivudine. It is available as tablets (150 and 300 mg) and as an oral solution (10 mg/ml).

What is Epivir used for?

Epivir is used in combination with other antiviral medicines to treat patients infected with human immunodeficiency virus (HIV), the virus that causes acquired immune deficiency syndrome (AIDS).

The medicine can only be obtained with a prescription.

How is Epivir used?

Treatment with Epivir should be started by a doctor who has experience in the management of HIV infection.

The recommended dose of Epivir for adults and children weighing at least 25 kg is 300 mg a day. This can be taken either as a single daily dose or divided into 150 mg twice a day. In children weighing less than 25 kg the recommended dose depends on their weight.

Patients who cannot swallow tablets should use the oral solution, or alternatively they may crush the tablets and add them to a small amount of food or drink immediately before swallowing it.

The dose of Epivir needs to be adjusted in patients who have severe kidney problems. The oral solution can be used to achieve the appropriate dose. For further information, see the package leaflet.

How does Epivir work?

The active substance in Epivir, lamivudine, is a nucleoside reverse transcriptase inhibitor (NRTI).It works by blocking the activity of reverse transcriptase, an enzyme needed by HIV to produce the genetic instructions for making more viruses once it has infected the cell. Epivir, taken in combination with other antiviral medicines, reduces the amount of HIV in the blood and keeps it at a low level. It does not cure HIV infection or AIDS, but it can hold off damage to the immune system and avoid the development of infections and diseases associated with AIDS.

How has Epivir been studied?

Epivir has been studied in five main studies involving almost 3,000 adults (aged 18 years or over).

Four of these studies compared Epivir in combination with zidovudine (another antiviral medicine) to either Epivir or zidovudine alone, or to the combination of Epivir and zalcitabine (another antiviral medicine). The studies examined the effects of Epivir on the levels of HIV in the blood (viral load) and the number of CD4 T‑cells in the blood (CD4 cell count). CD4 T‑cells are white blood cells that are important in helping to fight infections, but which are killed by HIV.

The fifth study compared the effects of adding Epivir or placebo (a dummy treatment) to existing treatment for HIV infection in 1,895 adults who had been taking antiviral medicines for at least four weeks. This study looked at how many patients had developed an illness associated with AIDS or had died after a year’s treatment.

Epivir has also been studied in 615 patients aged between nine months and 15 years. The study compared the effects of Epivir taken with zidovudine to didanosine (another antiviral medicine) taken alone. The study measured how long the patients lived without their disease getting worse.

What benefit has Epivir shown during the studies?

All of the studies found that combinations including Epivir were more effective than the comparator medicines.

In the first four studies in adults, Epivir, taken in combination with zidovudine, increased CD4 cell counts more than the comparator medicines after 24 weeks of treatment. The combination also reduced viral loads in all studies after two to four weeks of treatment, but this effect was temporary.

In the fifth adult study, adding Epivir to existing treatment reduced the risk of disease progression or death: after a year, 9% of the patients taking Epivir had developed an AIDS-related illness or died (128 out of 1,369), compared with 20% of those taking placebo (95 out of 471).

Similar results were seen in HIV-infected patients aged under 15 years.

What is the risk associated with Epivir?

The most common side effects with Epivir (seen in between 1 and 10 patients in 100) are diarrhoea, nausea (feeling sick), vomiting, headache, insomnia (difficulty sleeping), cough, nasal symptoms, rash, muscle disorders, arthralgia (joint pain), alopecia (hair loss), fever, abdominal pain (stomach ache) or cramps, malaise (feeling unwell) and fatigue (tiredness). For the full list of all side effects and restrictions with Epivir, see the package leaflet.

Why has Epivir been approved?

The CHMP decided that Epivir’s benefits are greater than its risks and recommended that it be given marketing authorisation.

What measures are being taken to ensure the safe and effective use of Epivir?

A risk management plan has been developed to ensure that Epivir is used as safely as possible. Based on this plan, safety information has been included in the summary of product characteristics and the package leaflet for Epivir, including the appropriate precautions to be followed by healthcare professionals and patients.

Other information about Epivir

The European Commission granted a marketing authorisation valid throughout the European Union for Epivir on 8 August 1996.

For more information about treatment with Epivir, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Name Language First published Last updated
Epivir : EPAR - Summary for the public BG = bălgarski 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public ES = español 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public CS = čeština 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public DA = dansk 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public DE = Deutsch 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public ET = eesti keel 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public EL = elliniká 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public EN = English 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public FR = français 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public IT = italiano 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public LV = latviešu valoda 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public LT = lietuvių kalba 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public HU = magyar 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public MT = Malti 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public NL = Nederlands 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public PL = polski 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public PT = português 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public RO = română 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public SK = slovenčina 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public SL = slovenščina 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public FI = suomi 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public SV = svenska 25/09/2008 07/05/2015
Epivir : EPAR - Summary for the public HR = Hrvatski 25/09/2008 07/05/2015

This EPAR was last updated on 07/05/2015 .

Authorisation details

Product details

Product details for Epivir
NameEpivir
Agency product numberEMEA/H/C/000107
Active substance

lamivudine

International non-proprietary name (INN) or common name

lamivudine

Therapeutic area HIV Infections
Anatomical therapeutic chemical (ATC) code J05AF05

Publication details

Publication details for Epivir
Marketing-authorisation holder

ViiV Healthcare UK Limited
 

Revision31
Date of issue of marketing authorisation valid throughout the European Union08/08/1996

Contact address:

ViiV Healthcare UK Limited
980 Great West Road
Brentford
Middlesex
TW8 9GS
United Kingdom

Product information

Product information

08/04/2015  Epivir -EMEA/H/C/000107 -IB/0094

Name Language First published Last updated
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Product Information HR = Hrvatski 02/12/2009 07/05/2015

Contents

  • Annex I - Summary of product characteristics
  • Annex IIA - Manufacturing-authorisation holder responsible for batch release
  • Annex IIB - Conditions of the marketing authorisation
  • Annex IIIA - Labelling
  • Annex IIIB - Package leaflet

Please note that the size of the above document can exceed 50 pages.

You are therefore advised to be selective about which sections or pages you wish to print.


Name Language First published Last updated
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  
Epivir : EPAR - All Authorised presentations HR = Hrvatski 07/03/2006  

Pharmacotherapeutic group

Antivirals for systemic use

Therapeutic indication

Epivir is indicated as part of antiretroviral combination therapy for the treatment of human-immunodeficiency-virus (HIV)-infected adults and children.

Assessment History

Changes since initial authorisation of medicine

Name Language First published Last updated
Epivir : EPAR - Procedural steps taken and scientific information after authorisation HR = Hrvatski 02/12/2009 07/05/2015
Epivir : EPAR - Steps taken after authorisation when a cutoff date has been used HR = Hrvatski 25/11/2005  

Initial marketing-authorisation documents

Name Language First published Last updated
Epivir : EPAR - Procedural steps taken before authorisation HR = Hrvatski 25/11/2005  
Epivir : EPAR - Scientific Discussion HR = Hrvatski 25/11/2005  

Authorised

This medicine is approved for use in the European Union