
Ask a doctor about a prescription for ENTECAVIR AUROVITAS 1 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
Entecavir Aurovitas 1 mg Film-Coated Tablets EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the Package Leaflet
Entecavir is an antiviral medicine used to treat long-term (chronic) infection with hepatitis B virus (HBV) in adults.
Entecavir may be used in patients whose liver is damaged but still works adequately (compensated liver disease) and in patients whose liver is damaged and does not work adequately (decompensated liver disease).
Entecavir is also used to treat chronic (long-term) HBV infection in children and adolescents from 2 to less than 18 years of age.
Entecavir may be used in children whose liver is damaged but still works adequately (compensated liver disease).
Hepatitis B virus infection can damage your liver. Entecavir reduces the amount of virus in your body and improves the condition of your liver.
Do not take Entecavir Aurovitas
Warnings and precautions
Tell your doctor or pharmacist before you start taking Entecavir Aurovitas:
Children and adolescents
Entecavir should not be used in children under 2 years of age or weighing less than 10 kg.
Other medicines and Entecavir Aurovitas
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Taking Entecavir Aurovitas with food and drinks
In most cases, you can take entecavir with or without food. However, if you have received previous treatment with another medicine containing lamivudine as the active substance, you should consider the following. If you have switched to entecavir because treatment with lamivudine was not successful, you should take entecavir on an empty stomach, once a day. If your liver disease is very advanced, your doctor will also instruct you on taking entecavir on an empty stomach.
Empty stomach means at least 2 hours after and 2 hours before the next meal.
Children and adolescents (from 2 to less than 18 years of age) can take entecavir with or without food.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
The use of entecavir has not been shown to be safe during pregnancy. Entecavir should not be used during pregnancy unless clearly necessary, as determined by your doctor. It is important that women of childbearing age using entecavir use an effective method of contraception to avoid becoming pregnant.
You should not breastfeed during treatment with entecavir. If you are breastfeeding, tell your doctor. It is not known whether entecavir, the active substance of this medicine, is excreted in breast milk.
Driving and using machines
Dizziness, fatigue, and drowsiness are common side effects that may affect your ability to drive and use machines. If you are unsure, consult your doctor.
Entecavir Aurovitas contains lactose
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
Not all patients need to take the same dose of entecavir.
Follow exactly the instructions of your doctor for taking this medicine. If you are unsure, consult your doctor or pharmacist.
For adults, the recommended dose is 0.5 mg or 1 mg once a day (by mouth).
Your dose will depend on:
For children and adolescents(from 2 to less than 18 years of age), your pediatrician will decide on the appropriate dose based on the child's body weight. Children weighing at least 32.6 kg can take the 0.5 mg tablets, or an oral solution may be available. For patients weighing between 10 kg and 32.5 kg, entecavir oral solution is recommended. All doses should be taken once a day (by mouth). There are no recommendations for entecavir in children under 2 years of age or weighing less than 10 kg.
Your pediatrician will decide on the appropriate dose based on the child's body weight.
Your doctor will advise you on the correct dose for you. Always take the dose recommended by your doctor to ensure that the medicine is fully effective and to reduce the development of resistance to treatment. Take entecavir for as long as your doctor tells you to. Your doctor will tell you when to stop treatment.
Some patients must take this medicine on an empty stomach (see Taking Entecavir Aurovitas with food and drinksin Section 2). If your doctor tells you to take this medicine on an empty stomach, empty stomach means at least 2 hours after a meal and 2 hours before the next meal.
If you take more Entecavir Aurovitas than you should
If you have taken more entecavir than you should, consult your doctor, pharmacist, or call the Toxicology Information Service, phone 91 562 04 20, indicating the medicine and the amount used.
If you forget to take Entecavir Aurovitas
It is important that you do not miss any dose. If you miss a dose of entecavir, take it as soon as possible and then take the next scheduled dose at the usual time. If it is almost time for your next dose, do not take the missed dose. Wait and take the next dose at the usual time. Do not take a double dose to make up for missed doses.
Do not stop treatment with Entecavir Aurovitas without consulting your doctor
Some people develop severe hepatitis symptoms when they stop taking entecavir. Tell your doctor immediately about any changes in symptoms you notice after stopping treatment.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Patients treated with entecavir have reported the following side effects:
Adults
? common (may affect up to 1 in 10 people): headache, insomnia, fatigue, dizziness, drowsiness, vomiting, diarrhea, nausea, dyspepsia, and increased levels of liver enzymes in the blood.
? uncommon (may affect up to 1 in 100 people): skin rash, hair loss.
? rare (may affect up to 1 in 1,000 people): severe allergic reaction.
If you experience side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet.
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 (may affect up to 1 in 10 people): low levels of neutrophils (a type of white blood cell 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 to the Spanish Medicines and Healthcare Products Agency (AEMPS) at www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
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, carton, and blister after EXP. The expiry date is the last day of the month stated.
Blister: Store below 30°C.
HDPE bottle: No special storage conditions are required.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Entecavir Aurovitas
Tablet core:lactose monohydrate, microcrystalline cellulose (E460), crospovidone (E1202), and magnesium stearate.
Tablet coating:hypromellose (E464), macrogol 400, and titanium dioxide (E171).
Appearance and packaging of the product
White, round, biconvex film-coated tablets with "ET" on one side and "1" on the other.
Entecavir Aurovitas film-coated tablets are available in blister packs and HDPE bottles.
Package sizes:
Blister:30 and 90 film-coated tablets.
HDPE bottles:30, 100, and 250 film-coated tablets.
Not all pack sizes may be marketed.
Marketing authorisation holder and manufacturer
Marketing authorisation holder:
Aurovitas Spain, S.A.U.
Avda. de Burgos, 16-D
28036 Madrid
Spain
Manufacturer:
APL Swift Services (Malta) Limited
HF26, Hal Far Industrial Estate, Hal Far
Birzebbugia, BBG 3000
Malta
Or
Arrow Génériques
26 Avenue Tony Garnier
69007 Lyon
France
Or
Generis Farmacêutica, S.A.
Rua João de Deus, 19
2700-487 Amadora
Portugal
This medicine is authorised in the Member States of the European Economic Area under the following names:
Germany:  | Entecavir PUREN 1 mg Filmtabletten  | 
Spain:  | Entecavir Aurovitas 1 mg comprimidos recubiertos con película EFG  | 
France:  | Entecavir Arrow 1mg, comprimé pelliculé  | 
Italy:  | Entecavir Aurobindo  | 
Netherlands:  | Entecavir Aurobindo 1 mg, filmomhulde tabletten  | 
Poland:  | Entecavir Aurovitas  | 
Portugal:  | Entecavir Generis  | 
Czech Republic:  | Entecavir Aurovitas  | 
Date of last revision of this leaflet:July 2021
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) (http://www.aemps.gob.es/).
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