Package Leaflet: Information for the User
Harvoni 90 mg/400 mg film-coated tablets
Harvoni 45 mg/200 mg film-coated tablets
ledipasvir/sofosbuvir
This medicine is subject to additional monitoring, which will help to quickly identify new safety information. You can contribute by reporting any side effects you may get. The last section of the leaflet includes information on how to report side effects.
Read all of this leaflet carefully before you start taking this medicine, because it contains important information for you.
Contents of the pack and other information
If Harvoni has been prescribed to your child, please note that all the information in this leaflet is intended for your child (in that case, read ‘your child’ instead of ‘you’).
Harvoni is a medicine that contains the active substances ledipasvir and sofosbuvir. Harvoni is used to treat long-term hepatitis C virus infection in adultsand children aged 3 years and older.
Hepatitis C is a viral infection of the liver. The active substances in the medicine work together by blocking two different proteins that the virus needs to grow and multiply, allowing the infection to be eliminated from the body.
Harvoni is sometimes taken with another medicine: ribavirin.
It is very important that you also read the package leaflets of any other medicines that you are taking with Harvoni. If you have any questions about your medicines, ask your doctor or pharmacist.
Do not take Harvoni
Warnings and precautions
Your doctor will know if you have any of the following conditions. They will be taken into account before starting treatment with Harvoni.
Tell your doctor or pharmacist before starting treatment with Harvoni if:
Tell your doctor immediatelyif you are currently taking or have taken in the last few months any medicine for heart problems and, during treatment, you experience:
Blood tests
Your doctor will perform blood tests before, during, and after treatment with Harvoni. This is to:
Children and adolescents
Do not give this medicine to children under 3 years of age. The use of Harvoni has not been studied in children under 3 years of age.
Other medicines and Harvoni
Tell your doctor or pharmacistif you are taking, have recently taken or might take any other medicines.
Warfarin and other similar medicines known as vitamin K antagonists, used to thin the blood. Your doctor may increase the number of blood tests to check how your blood clots.
Your liver function may change with hepatitis C treatment, and this may affect other medicines (e.g. medicines used to suppress your immune system, etc.). Your doctor may need to closely monitor these other medicines you are taking and make adjustments after starting treatment with Harvoni.
If you are not sure if you should take any other medicine, ask your doctor or pharmacist.
Some medicines must not be taken with Harvoni.
Taking Harvoni with any of these medicines may stop them from working properly or make any side effects worse. Your doctor may need to give you a different medicine or adjust the dose of the one you are taking.
These medicines may reduce the amount of ledipasvir in the blood. If you are taking any of these medicines, your doctor will give you a different medicine for stomach ulcers, heartburn or acid reflux or advise you on how and when to take it.
Pregnancy and contraception
The effects of Harvoni during pregnancy are not known. If you are pregnant, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.
Pregnancy should be avoided if you are taking Harvoni with ribavirin. It is very important that you carefully read the section "Pregnancy" in the package leaflet of ribavirin. Ribavirin can be very harmful to the unborn baby. Special precautions should be taken in sexual activity if there is any possibility of pregnancy.
Breast-feeding
Do not breast-feed during treatment with Harvoni.It is not known if ledipasvir or sofosbuvir, the two active substances of Harvoni, pass into human breast milk.
Driving and using machines
If you feel tired after taking Harvoni, do not perform activities that require concentration, such as driving, cycling or using machines.
Harvoni 90 mg/400 mg and 45 mg/200 mg film-coated tablets contain lactose
Harvoni 90 mg/400 mg film-coated tablets contain orange yellow S (E110) which may cause allergic reactions
Take this medicine exactly as your doctor has told you.
If you are not sure, ask your doctor or pharmacist.
Recommended dose
You must take Harvoni as directed by your doctor.The recommended dose of Harvoni in adultsis one 90 mg/400 mg film-coated tablet once a day. Your doctor will tell you how many weeks you need to take Harvoni.
The recommended dose of Harvoni in children aged 3 years and older is based on weight.
Take Harvoni as directed by your doctor.
Swallow the tablet(s) whole, with or without food. Do not chew, crush or break the tablet, as it has a very bitter taste. Tell your doctor or pharmacist if you have problems swallowing the tablets.
If you are taking an antacid,take it at least 4 hours before or at least 4 hours after Harvoni.
If you are taking a proton pump inhibitor,take the proton pump inhibitor at the same time as Harvoni. Do not take it before Harvoni.
If you vomit after taking Harvonithis may affect the amount of Harvoni in the blood. This may make Harvoni work less well.
If you take more Harvoni than you should
If you accidentally take more than the recommended dose, contact your doctor or the nearest emergency department immediately for advice. Take the pack of tablets with you to show the doctor what you have taken.
If you forget to take Harvoni
It is important that you do not miss any dose of this medicine.
If you miss a dose, calculate how long it has been since you took your last Harvoni:
Do not stop treatment with Harvoni
Do not stop treatment with this medicine unless your doctor tells you to. It is very important that you complete the full treatment course so that the medicine can work as well as possible to treat the hepatitis C virus infection.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you take Harvoni, you may experience one or more of the following side effects:
Very common side effects
(may affect more than 1 in 10 people)
Common side effects
(may affect up to 1 in 10 people)
Other side effects that may occur during treatment with Harvoni
The frequency of the following side effects cannot be estimated from the available data.
Other side effects that may occur during treatment with sofosbuvir:
The frequency of the following side effects cannot be estimated from the available data.
Reporting of side effects
If you experience 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 national reporting system listed in Appendix V. 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 carton and blister after "EXP". The expiry date refers to the last day of the month stated.
This medicine does not require any special storage conditions.
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 Harvoni
Copovidone, lactose monohydrate, microcrystalline cellulose, sodium croscarmellose, anhydrous colloidal silica, magnesium stearate
Film coating:
Polyvinyl alcohol, titanium dioxide, macrogol, talc, and only for the 90 mg/400 mg tablet; Orange Yellow FCF (E110)
Appearance of the Product and Container Content
Harvoni 90 mg/400 mg film-coated tablets are orange, rhombus-shaped tablets with "GSI" engraved on one side and "7985" on the other. The tablet measures approximately 19 mm in length and 10 mm in width.
Harvoni 45 mg/200 mg film-coated tablets are white, capsule-shaped tablets with "GSI" engraved on one side and "HRV" on the other. The tablet measures approximately 14 mm in length and 7 mm in width.
Each bottle contains a silica gel desiccant (drying agent) that should be kept in the bottle to help protect the tablets. The silica gel desiccant is packaged in a separate pouch or container and should not be swallowed.
The following package sizes are available:
Marketing Authorization Holder
Gilead Sciences Ireland UC
Carrigtohill
County Cork, T45 DP77
Ireland
Manufacturer
Gilead Sciences Ireland UC
IDA Business & Technology Park
Carrigtohill
County Cork
Ireland
For further information on this medicinal product, please contact the local representative of the marketing authorization holder:
Belgium Gilead Sciences Belgium SPRL-BVBA Tel: + 32 (0) 24 01 35 50 | Lithuania Gilead Sciences Poland Sp. z o.o. Tel: + 48 22 262 8702 |
Bulgaria Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1888 | Luxembourg Gilead Sciences Belgium SPRL-BVBA Tel: + 32 (0) 24 01 35 50 |
Czech Republic Gilead Sciences s.r.o. Tel: + 420 910 871 986 | Hungary Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1888 |
Denmark Gilead Sciences Sweden AB Tel: + 46 (0) 8 5057 1849 | Malta Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1888 |
Germany Gilead Sciences GmbH Tel: + 49 (0) 89 899890-0 | Netherlands Gilead Sciences Netherlands B.V. Tel: + 31 (0) 20 718 36 98 |
Estonia Gilead Sciences Poland Sp. z o.o. Tel: + 48 22 262 8702 | Norway Gilead Sciences Sweden AB Tel: + 46 (0) 8 5057 1849 |
Greece Gilead Sciences Ελλάς Μ.ΕΠΕ. Tel: + 30 210 8930 100 | Austria Gilead Sciences GesmbH Tel: + 43 1 260 830 |
Spain Gilead Sciences, S.L. Tel: + 34 91 378 98 30 | Poland Gilead Sciences Poland Sp. z o.o. Tel: + 48 22 262 8702 |
France Gilead Sciences Tel: + 33 (0) 1 46 09 41 00 | Portugal Gilead Sciences, Lda. Tel: + 351 21 7928790 |
Croatia Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1888 | Romania Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1888 |
Ireland Gilead Sciences Ireland UC Tel: + 353 (0) 214 825 999 | Slovenia Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1888 |
Iceland Gilead Sciences Sweden AB Tel: + 46 (0) 8 5057 1849 | Slovakia Gilead Sciences Slovakia s.r.o. Tel: + 421 232 121 210 |
Italy Gilead Sciences S.r.l. Tel: + 39 02 439201 | Finland Gilead Sciences Sweden AB Tel: + 46 (0) 8 5057 1849 |
Cyprus Gilead Sciences Ελλάς Μ.ΕΠΕ. Tel: + 30 210 8930 100 | Sweden Gilead Sciences Sweden AB Tel: + 46 (0) 8 5057 1849 |
Latvia Gilead Sciences Poland Sp. z o.o. Tel: + 48 22 262 8702 | United Kingdom Gilead Sciences Ltd. Tel: + 44 (0) 8000 113700 |
Date of Last Revision of this Leaflet:
Detailed information on this medicinal product is available on the European Medicines Agency website: http://www.ema.europa.eu