Package Leaflet: Information for the User
Erleada 240 mg Film-Coated Tablets
apalutamide
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
What is Erleada
Erleada is a cancer medicine that contains the active substance apalutamide.
What is Erleada used for
It is used to treat adult men with prostate cancer that:
How Erleada works
Erleada works by blocking the activity of hormones called androgens (such as testosterone). Androgens can cause the growth of prostate cancer. By blocking the effect of androgens, apalutamide makes prostate cancer cells stop growing and dividing.
Do not take Erleada
Do not take this medicine if any of the above applies to you. If you are not sure, consult your doctor or pharmacist before taking this medicine.
Warnings and precautions
Consult your doctor or pharmacist before starting to take this medicine if:
If any of the above applies to you (or you are not sure), consult your doctor or pharmacist before taking this medicine.
Falls and bone fractures
Falls have been observed in patients taking Erleada. Take special precautions to reduce the risk of falls. Bone fractures have been observed in patients taking this medicine.
Heart disease, stroke, or mini-stroke
Some people have suffered a blockage of the heart arteries or part of the brain that can cause death during treatment with Erleada.
Your doctor will monitor you for signs and symptoms of heart or brain problems during treatment with this medicine.
Call your doctor or go immediately to the nearest emergency center if you have:
If you are taking any medicine, consult your doctor or pharmacist to see if it is associated with a higher risk of seizures, bleeding, or heart problems.
Severe skin reactions (SSR)
There have been reports of severe skin reactions, including drug reaction with eosinophilia and systemic symptoms (DRESS) or Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with the use of Erleada. DRESS may appear as a widespread rash, high body temperature, and swollen lymph nodes. SJS/TEN may appear initially on the trunk as red target-like patches or circular patches that often have central blisters. Additionally, ulcers can occur in the mouth, throat, nose, genitals, and eyes (red and swollen eyes). These severe skin rashes often precede fever and/or flu-like symptoms. The rashes can progress to widespread skin peeling and potentially life-threatening complications.
If you develop a severe rash or any of these skin symptoms, stop taking this medicine and contact your doctor immediately.
If any of the above applies to you (or you are not sure), consult your doctor or pharmacist before taking this medicine. See the section "Serious side effects" in section 4 for more information.
Children and adolescents
This medicine must not be used in children and adolescents under 18 years of age.
If a child or young person accidentally takes this medicine:
Other medicines and Erleada
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, as Erleada may affect the way other medicines work. Also, other medicines may affect the way Erleada works.
In particular, tell your doctor if you are taking medicines for:
You should make a list of the names of the medicines you are taking and show it to your doctor or pharmacist when you start taking a new medicine. Tell your doctor that you are taking Erleada if your doctor wants to start any new treatment. It may be necessary to change the dose of Erleada or any of the other medicines you are taking.
Pregnancy and contraception information for men and women
Information for women
Information for men: follow these guidelines during treatment and up to 3 months after stopping treatment
Use contraceptives during treatment and up to 3 months after stopping treatment. Consult your doctor if you have any questions about contraception.
This medicine may reduce male fertility.
Driving and using machines
Erleada is unlikely to affect your ability to drive or use any tools or machines.
The side effects of this medicine include seizures. If you are at higher risk of seizures (see Section 2, 'Warnings and precautions'), consult your doctor.
Erleada contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per 240 mg dose (1 tablet); this is essentially 'sodium-free'.
Follow the instructions for administration of this medicine exactly as told by your doctor. If you are unsure, consult your doctor or pharmacist again.
Your doctor may prescribe other medicines while you are taking Erleada.
How much to take
The recommended dose of this medicine is 240 mg (1 tablet) once a day.
How to take Erleada
If you cannot swallow the tablet whole
If you take more Erleada than you should
If you take more than you should, stop taking this medicine and contact your doctor.
You may have a higher risk of side effects.
If you forget to take Erleada
If you forget to take this medicine, take your usual dose as soon as you remember on the same day.
If you stop taking Erleada
Do not stop taking this medicine without consulting your doctor first.
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.
Serious side effects
Stop taking Erleada and seek medical attention immediately if you notice any of the following symptoms:
Tell your doctor immediately if you notice any of the following serious side effects, your doctor may stop treatment:
Very common:may affect more than 1 in 10 people
Common:may affect up to 1 in 10 people
Uncommon:may affect up to 1 in 100 people
Tell your doctor immediately if you notice any of the serious side effects mentioned above.
Side effects include
Tell your doctor immediately if you notice any of the following side effects:
Very common(may affect more than 1 in 10 people):
Common(may affect up to 1 in 10 people):
Uncommon(may affect up to 1 in 100 people):
Rare(may affect up to 1 in 1,000 people):
Tell your doctor immediately if you notice any of the side effects mentioned above.
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 after EXP. The expiry date refers to the last day of the month shown.
Store in the original package to protect from moisture. This medicine does not require any special storage temperature.
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 Erleada
Appearance and Container Content of the Product
Erleada film-coated tablets are blue-grey to grey, oval-shaped (21 mm long by 10 mm wide), with “E240” engraved on one side.
The tablets may be presented in a bottle or a blister pack. Only certain pack sizes may be marketed.
Bottle
The tablets are presented in a plastic bottle with a child-resistant closure. Each bottle contains 30 tablets and a total of 2 g of desiccant. Each carton contains one bottle. Store in the original packaging. Do not ingest or discard the desiccant.
28-Day Box
Each 28-day box contains 28 film-coated tablets in 2 cardboard blisters of 14 film-coated tablets each.
30-Day Box
Each 30-day box contains 30 film-coated tablets in 3 cardboard blisters of 10 film-coated tablets each.
Marketing Authorisation Holder
Janssen-Cilag International NV
Turnhoutseweg 30
B-2340 Beerse
Belgium
Manufacturer
Janssen Cilag SpA
Via C. Janssen
Borgo San Michele
Latina 04100, Italy
For further information about this medicinal product, please contact the local representative of the marketing authorisation holder:
België/Belgique/Belgien Janssen-Cilag NV Tel/Tél: +32 14 64 94 11 janssen@jacbe.jnj.com | Lietuva UAB "JOHNSON & JOHNSON" Tel: +370 5 278 68 88 lt@its.jnj.com |
jjsafety@its.jnj.com | Luxembourg/Luxemburg Janssen-Cilag NV Tél/Tel: +32 14 64 94 11 janssen@jacbe.jnj.com |
Ceská republika Janssen-Cilag s.r.o. Tel.: +420 227 012 227 | Magyarország Janssen-Cilag Kft. Tel.: +36 1 884 2858 janssenhu@its.jnj.com |
Danmark Janssen-Cilag A/S Tlf: +45 4594 8282 jacdk@its.jnj.com | Malta AM MANGION LTD. Tel: +356 2397 6000 |
Deutschland Janssen-Cilag GmbH Tel: +49 2137 955 955 jancil@its.jnj.com | Nederland Janssen-Cilag B.V. Tel: +31 76 711 1111 janssen@jacnl.jnj.com |
Eesti UAB "JOHNSON & JOHNSON" Eesti filiaal Tel: +372 617 7410 ee@its.jnj.com | Norge Janssen-Cilag AS Tlf: +47 24 12 65 00 jacno@its.jnj.com |
Österreich Janssen-Cilag Pharma GmbH Tel: +43 1 610 300 | |
España Janssen-Cilag, S.A. Tel: +34 91 722 81 00 contacto@its.jnj.com | Polska Janssen-Cilag Polska Sp. z o.o. Tel.:+48 22 237 60 00 |
France Janssen-Cilag Tél: 0 800 25 50 75 / +33 1 55 00 40 03 medisource@its.jnj.com | Portugal Janssen-Cilag Farmacêutica, Lda. Tel: +351 214 368 600 |
Hrvatska Johnson & Johnson S.E. d.o.o. Tel: +385 1 6610 700 jjsafety@JNJCR.JNJ.com | România Johnson & Johnson România SRL Tel: +40 21 207 1800 |
Ireland Janssen Sciences Ireland UC Tel: 1 800 709 122 medinfo@its.jnj.com | Slovenija Johnson & Johnson d.o.o. Tel: +386 1 401 18 00 Janssen_safety_slo@its.jnj.com |
Ísland Janssen-Cilag AB c/o Vistor hf. Sími: +354 535 7000 janssen@vistor.is | Slovenská republika Johnson & Johnson, s.r.o. Tel: +421 232 408 400 |
Italia Janssen-Cilag SpA Tel: 800.688.777 / +39 02 2510 1 janssenita@its.jnj.com | Suomi/Finland Janssen-Cilag Oy Puh/Tel: +358 207 531 300 jacfi@its.jnj.com |
Sverige Janssen-Cilag AB Tfn: +46 8 626 50 00 jacse@its.jnj.com | |
Latvija UAB "JOHNSON & JOHNSON" filiale Latvija Tel: +371 678 93561 lv@its.jnj.com | United Kingdom (Northern Ireland) Janssen Sciences Ireland UC Tel: +44 1 494 567 444 medinfo@its.jnj.com |
Date of the Last Revision of this Leaflet:
Other Sources of Information
Detailed information on this medicinal product is available on the European Medicines Agency website: http://www.ema.europa.eu/, and on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/).