Package Leaflet: Information for the User
Descovy 200 mg/10 mg film-coated tablets
emtricitabine/tenofovir alafenamide
This medicine is subject to additional monitoring, which will allow for quick identification of new safety information. You can help by reporting any side effects you may get. The last section of this 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
Descovy contains two active substances:
Descovy blocks the action of an enzyme called reverse transcriptase, which is essential for the multiplication of the virus. Therefore, Descovy reduces the amount of HIV present in the body.
Descovy, in combination with other medicines, is used to treat HIV-1 infectionin adults and adolescents aged 12 years and older, who weigh at least 35 kg.
Do not take Descovy:
Warnings and precautions
You must remain under the supervision of your doctor while taking Descovy.
While taking this medicine, you can still transmit HIV to others, even if effective antiretroviral therapy reduces the risk. Consult your doctor about the precautions needed to avoid infecting others. This medicine is not a cure for HIV infection. While you are taking Descovy, you may still experience infections or illnesses associated with HIV.
Consult your doctor before taking Descovy:
If you have hepatitis B, liver problems may get worse once you stop taking Descovy. Do not stop taking Descovy without talking to your doctor first: see section 3, Do not stop taking Descovy.
While taking Descovy
Once you start taking Descovy, be aware of:
Although kidney problems have not been observed with Descovy, there is a possibility that you may experience kidney problems if you take Descovy for a long time.
Children and adolescents
Do not give this medicine to childrenaged 11 years or younger or weighing less than 35 kg.
Descovy has not been studied in children aged 11 years or younger.
Other medicines and Descovy
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.Descovy may interact with other medicines. As a result, the levels of Descovy or other medicines in your blood may change. This may prevent your medicines from working properly or increase the risk of side effects. In some cases, your doctor may need to adjust the dose or check your blood levels.
Medicines used to treat hepatitis B infection:
Do not take Descovy with medicines that contain:
Other types of medicines:
Consult your doctor if you are taking:
Pregnancy and breastfeeding
Consult your doctor or pharmacist before using any medicine if you are pregnant.
If you have taken Descovy during your pregnancy, your doctor may ask for regular 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 side effects.
Do not breastfeed your child while taking Descovy.This is because one of the active substances in this medicine passes into breast milk. Breastfeeding is not recommended to avoid transmitting the virus to your child through breast milk.
Driving and using machines
Descovy may cause dizziness. If you feel dizzy while taking Descovy, do not drive or operate tools or machines.
Take this medicine exactly as your doctor has told you.
If you are not sure, consult your doctor or pharmacist again.
The recommended dose is:
Adults:one tablet a day, with or without food
Adolescents aged 12 years or older, weighing at least 35 kg:one tablet a day, with or without food
Do not chew, crush, or split the tablet.
Always take the dose recommended by your doctor.This is to ensure that your medicine is fully effective and to reduce the risk of developing resistance to treatment. Do not change the dose unless your doctor tells you to.
If you are on dialysis,take the daily dose of Descovy after dialysis.
If you take more Descovy than you should
If you take more than the recommended dose of Descovy, you may be at greater risk of side effects from this medicine (see section 4, Possible side effects).
Consult your doctor immediately or go to the nearest emergency room. Take the pack of tablets with you to show what you have taken.
If you forget to take Descovy
It is important that you do not miss a dose of Descovy.
If you forget a dose:
If you vomit within 1 hour after taking Descovy,take another tablet.
Do not stop taking Descovy
Do not stop taking Descovy without talking to your doctor first.Stopping Descovy may seriously affect the success of future treatments. If you stop Descovy for any reason, consult your doctor before restarting Descovy.
When you notice that you have little Descovy left,go to your doctor or pharmacist to get more. This is very important, as the amount of virus may start to increase if the medicine is stopped, even for a short time. Your disease may then become more difficult to treat.
If you have both HIV and hepatitis B infection,it is very important not to stop taking Descovy without first talking to your doctor. You may need to have blood tests for several months after stopping treatment. In some patients with advanced liver disease or cirrhosis, stopping treatment can cause the hepatitis to get worse, which can be life-threatening.
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.
Serious side effects: tell a doctor immediately
Autoimmune disorders (where the immune system attacks healthy body tissues) may also occur after starting treatment for HIV. Autoimmune disorders may occur many months after starting treatment. Be aware of any symptoms of infection or other symptoms such as:
Very common side effects
(may affect more than 1 in 10 people)
Common side effects
(may affect up to 1 in 10 people)
Uncommon side effects
(may affect up to 1 in 100 people)
Other effects that may be seen during HIV treatment
The frequency of the following side effects is not known (the frequency cannot be estimated from the available data).
During HIV treatment, there may be an increase in weight and levels of glucose and lipids in the blood. This may be partly due to the recovery of health and, in the case of blood lipids, sometimes due to the HIV medicines themselves. Your doctor will monitor these changes.
Reporting 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 the 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.
Store in the original package to protect from moisture. Keep the bottle tightly closed.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active ingredients areemtricitabine and tenofovir alafenamide. Each Descovy film-coated tablet contains 200 mg of emtricitabine and tenofovir alafenamide fumarate equivalent to 10 mg of tenofovir alafenamide.
The other ingredients are
Tablet core:
Microcrystalline cellulose, sodium croscarmellose, magnesium stearate.
Film coating:
Polyvinyl alcohol, titanium dioxide, macrogol 3350, talc, iron oxide black (E172).
Appearance and Packaging of the Product
Descovy film-coated tablets are gray, rectangular tablets, marked on one side with “GSI” and on the other with the number “210”.
Descovy is available in bottles of 30 tablets (with a desiccant packet of silica gel that should be kept in the bottle to help protect the tablets). The desiccant packet of silica gel is contained in a separate pouch or container and should not be swallowed.
This medicinal product is available in packs of 1 bottle of 30 film-coated tablets and in packs of 60 (2 bottles of 30) and 90 (3 bottles of 30) film-coated tablets. Not all pack sizes may be marketed.
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:
België/Belgique/BelgienLietuva
Gilead Sciences Belgium SPRL-BVBA Gilead Sciences Poland Sp. z o.o.
Tel: + 32 (0) 24 01 35 50 Tel: +48 22 262 8702
????????Luxembourg/Luxemburg
Gilead Sciences Ireland UC Gilead Sciences Belgium SPRL-BVBA
Tel: + 353 (0) 1 686 1888 Tel: + 32 (0) 24 01 35 50
Česká republikaMagyarország
Gilead Sciences s.r.o. Gilead Sciences Ireland UC
Tel: + 420 910 871 986 Tel: + 353 (0) 1 686 1888
DanmarkMalta
Gilead Sciences Sweden AB Gilead Sciences Ireland UC
Tlf: + 46 (0) 8 5057 1849 Tel: + 353 (0) 1 686 1888
DeutschlandNederland
Gilead Sciences GmbH Gilead Sciences Netherlands B.V.
Tel: + 49 (0) 89 899890-0 Tel: + 31 (0) 20 718 36 98
EestiNorge
Gilead Sciences Poland Sp. z o.o. Gilead Sciences Sweden AB
Tel: +48 22 262 8702 Tlf: + 46 (0) 8 5057 1849
ΕλλάδαÖsterreich
Gilead Sciences Ελλάς Μ.ΕΠΕ. Gilead Sciences GesmbH
Τηλ: + 30 210 8930 100 Tel: + 43 1 260 830
EspañaPolska
Gilead Sciences, S.L. Gilead Sciences Poland Sp. z o.o.
Tel: + 34 91 378 98 30 Tel: +48 22 262 8702
FrancePortugal
Gilead Sciences Gilead Sciences, Lda.
Tél: + 33 (0) 1 46 09 41 00 Tel: + 351 21 7928790
HrvatskaRomânia
Gilead Sciences Ireland UC Gilead Sciences Ireland UC
Tel: + 353 (0) 1 686 1888 Tel: + 353 (0) 1 686 1888
IrelandSlovenija
Gilead Sciences Ireland UC Gilead Sciences Ireland UC
Tel: +353 (0) 214 825 999 Tel: + 353 (0) 1 686 1888
ÍslandSlovenská republika
Gilead Sciences Sweden AB Gilead Sciences Slovakia s.r.o.
Sími: + 46 (0) 8 5057 1849 Tel: + 421 232 121 210
ItaliaSuomi/Finland
Gilead Sciences S.r.l. Gilead Sciences Sweden AB
Tel: + 39 02 439201 Puh/Tel: + 46 (0) 8 5057 1849
ΚύπροςSverige
Gilead Sciences Ελλάς Μ.ΕΠΕ. Gilead Sciences Sweden AB
Τηλ: + 30 210 8930 100 Tel: + 46 (0) 8 5057 1849
LatvijaUnited Kingdom
Gilead Sciences Poland Sp. z o.o. Gilead Sciences Ltd.
Tel: +48 22 262 8702 Tel: + 44 (0) 8000 113 700
Date of Last Revision of this Leaflet:<{MM/AAAA}> <{month AAAA}>.
Detailed information on this medicinal product is available on the European Medicines Agency website: http://www.ema.europa.eu.