Enzalutamide Accord 40 mg soft capsules EFG
Enzalutamide Accord contains the active substance enzalutamide. Enzalutamide Accord is used to treat adult men with prostate cancer that:
or
How Enzalutamide Accord works
Enzalutamide Accord is a medicine that works by blocking the activity of certain hormones called androgens (such as testosterone). By blocking androgens, enzalutamide makes prostate cancer cells stop growing and dividing.
Do not take Enzalutamide Accord
Warnings and precautions
Seizures
Seizures have been reported in 5 out of every 1,000 people taking enzalutamide, and in less than 3 out of every 1,000 people taking placebo (see "Using Enzalutamide Accord with other medicines" below and "Possible side effects" in section 4).
If you are taking a medicine that can cause seizures or increase the risk of having seizures (see below "Other medicines and Enzalutamide Accord").
If you have a seizure during treatment:
Consult your doctor as soon as possible. Your doctor may decide that you should stop taking enzalutamide.
Posterior Reversible Encephalopathy Syndrome (PRES)
Rare cases of PRES, a rare, reversible disease that affects the brain, have been reported in patients treated with enzalutamide. If you have a seizure, worsening headache, confusion, blindness, or other vision problems, contact your doctor as soon as possible. (See also section 4 "Possible side effects").
Risk of new cancers (second primary malignancies)
There have been reports of new (second) cancers in patients treated with enzalutamide, including bladder and colon cancer.
Consult your doctor as soon as possible if you notice any signs of gastrointestinal bleeding, blood in your urine, or frequently feel an urgent need to urinate while taking enzalutamide.
Consult your doctor before starting to take Enzalutamide Accord
Tell your doctor if you have:
Any heart or blood vessel problems, including heart rhythm problems (arrhythmias), or if you are being treated with medicines to correct these problems. The risk of heart rhythm problems may be increased with the use of this medicine.
If you are allergic to enzalutamide, its administration could cause a rash or inflammation of the face, tongue, lips, or throat. If you are allergic to enzalutamide or any of the other ingredients of this medicine, do not take enzalutamide.
Severe skin rashes or peeling of the skin, blistering, and/or ulcers in the mouth have been reported in association with enzalutamide treatment. Seek medical attention immediately if you notice any of these symptoms.
If any of the above applies to you or if you are unsure, consult your doctor before taking this medicine.
Children and adolescents
This medicine should not be given to children or adolescents.
Other medicines and Enzalutamide Accord
Tell your doctor if you are taking, have recently taken, or might take any other medicines. You need to know the names of the medicines you are taking. Carry a list of them with you to show your doctor when they prescribe you a new medicine. Do not start or stop taking any medicine before consulting the doctor who prescribed this medicine.
Tell your doctor if you are taking any of the following medicines. These medicines may increase the risk of having a seizure when taken with enzalutamide:
Tell your doctor if you are taking the following medicines. These medicines may affect the effect of enzalutamide or enzalutamide may affect the effect of these medicines.
This includes certain medicines used to:
Enzalutamide may interfere with some medicines used to treat heart rhythm problems (e.g., quinidine, procainamide, amiodarone, and sotalol) or may increase the risk of heart rhythm problems when used with certain medicines (e.g., methadone [used for pain relief and as part of drug detoxification], moxifloxacin [an antibiotic], antipsychotics [used for severe mental illnesses]).
Tell your doctor if you are taking any of the above medicines. It may be necessary to adjust the dose of enzalutamide or any other medicine you are taking.
Pregnancy, breastfeeding, and fertility
Driving and using machines
The influence of enzalutamide on the ability to drive and use machines may be moderate. Seizures have been reported in patients who have taken enzalutamide. If you are at a higher risk of having seizures, you should consult your doctor.
Enzalutamide Accord contains sorbitol
This medicine contains 47.8 mg of sorbitol (E 420) in each soft capsule.
Follow the instructions for administration of this medicine exactly as indicated by your doctor. If you are unsure, consult your doctor again.
The recommended dose is 160 mg (four soft capsules), taken at the same time once a day.
How to take Enzalutamide Accord
It is also possible that your doctor may prescribe other medicines while you are taking enzalutamide.
If you take more Enzalutamide Accord than you should
If you take more soft capsules than prescribed, stop taking enzalutamide and contact your doctor. You may have a higher risk of having a seizure or other side effects.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medicine and the amount taken.
If you forget to take Enzalutamide Accord
If you stop taking Enzalutamide Accord
Do not stop taking this medicine unless your doctor tells you to.
If you have any further questions about the use of this medicine, ask your doctor.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Seizures
Seizures have been reported in 5 out of every 1,000 people taking enzalutamide, and in less than 3 out of every 1,000 people taking placebo.
Seizures are more likely if you take a higher dose of this medicine than recommended, if you take certain medicines, or if you have a higher risk of having seizures.
If you have a seizure, consult your doctor as soon as possible. Your doctor may decide that you should stop taking enzalutamide.
Posterior Reversible Encephalopathy Syndrome (PRES)
Rare cases of PRES (affecting up to 1 in 1,000 people), a rare, reversible disease that affects the brain, have been reported in patients treated with enzalutamide. If you have a seizure, worsening headache, confusion, blindness, or other vision problems, contact your doctor as soon as possible.
Other possible side effects are:
Very common(may affect more than 1 in 10 people) Fatigue, falls, bone fractures, hot flushes, high blood pressure
Common(may affect up to 1 in 10 people)
Headache, feeling anxious, dry skin, itching, difficulty remembering, blockage of the heart arteries (ischemic heart disease), increase in breast size in men (gynecomastia), restless legs syndrome, loss of concentration, memory loss, change in taste
Uncommon(may affect up to 1 in 100 people)
Hallucinations, difficulty thinking clearly, low white blood cell count
Not known(frequency cannot be estimated from the available data)
Muscle pain, muscle spasms, muscle weakness, back pain, changes in the electrocardiogram (QT interval prolongation), stomach upset including feeling sick (nausea), a skin reaction that causes red spots or patches on the skin, which may look like a target or a "bull's eye" with a dark red center surrounded by lighter red rings (erythema multiforme), rash, vomiting, swelling of the face, lips, tongue, and/or throat, decrease in the number of platelets in the blood (which increases the risk of bleeding or bruising), diarrhea
Reporting side effects
If you experience any side effects, consult your doctor, even if they are not listed in this leaflet. You can also report them directly through the Spanish Medicines Agency's online reporting system: https://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 stated on the outer packaging and on the blister pack after "EXP". The expiry date is the last day of the month shown.
This medicine does not require any special storage conditions.
Do not take any soft capsule that has lost its contents, is damaged, or shows signs of tampering.
Medicines should not be disposed of via wastewater or household waste. Return the packaging and any unused medicine to a pharmacy for proper disposal. If you are unsure, ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Composition of Enzalutamide Accord
Appearance of the product and pack contents
Not all pack sizes may be marketed.
Marketing authorisation holder and manufacturer
Marketing authorisation holder
Accord Healthcare S.L.U.
World Trade Center
Moll de Barcelona s/n,
Edifici Est, 6ª planta,
08039 Barcelona,
Spain
Manufacturers:
Pharmadox Healthcare Ltd.
KW20A Kordin Industrial Park, Paola
Malta
Or
Accord Healthcare Polska Sp.z.o.o.
Ul.Lutomierska 50,
95-200, Pabianice,
Poland
Or
Accord Healthcare B.V.
Winthontlaan 200,
3526 KV Utrecht,
Netherlands
or
Accord Healthcare single member S.A.
64th Km National Road Athens,
Lamia, Schimatari,
32009, Greece
This leaflet was last revised in: March 2024
Other sources of information
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS): http://www.aemps.gob.es/