CONCERTA 36 mg PROLONGED-RELEASE TABLETS

Introduction

Package Leaflet: Information for the User

Concerta 36 mg prolonged-release tablets

Methylphenidate, hydrochloride

Read the entire package leaflet carefully before you or your child start taking this medicine, as it contains important information for you.

• Keep this package leaflet, as you may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you or your child only. Do not give it to others, as it may harm them, even if they have the same symptoms of illness as you or your child.
• If you experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this package leaflet. See section 4.

Contents of the package leaflet

1. What is Concerta and what is it used for
2. What you need to know before you or your child take Concerta
3. How to take Concerta
4. Possible side effects
5. Storing Concerta
6. Package contents and further information

1. What is Concerta and what is it used for

What is it used for

Concerta is used to treat “Attention Deficit Hyperactivity Disorder” (ADHD).

• It is used in children from 6 years of age and in adults.
• It is used only after non-medication treatments, such as behavioral therapy and counseling, have been tried first.

Concerta is not indicated for the treatment of ADHD in children under 6 years of age.

How it works

Concerta improves the activity of certain parts of the brain that are underactive. The medication may help improve attention (level of attention), concentration, and reduce impulsive behavior.

The medication is given as part of a comprehensive treatment program, which usually includes:

• psychological therapy
• educational therapy and
• social therapy.

It is only prescribed by doctors who have experience in behavioral problems in children, adolescents, or adults. If you are an adult and have not received treatment before, the specialist will perform tests to confirm that you have had ADHD since childhood. Although ADHD has no cure, it can be controlled using comprehensive treatment programs.

About ADHD

Children and adolescents with ADHD have difficulty:

• staying still and
• focusing

It is not their fault that they cannot do these things.

Many children and adolescents struggle to do these things. However, ADHD can cause problems in daily life. Children and adolescents with ADHD may have difficulty learning and doing homework. They have difficulty behaving well at home, at school, and in other places.

Adults with ADHD often have difficulty concentrating. They often feel restless, impatient, and distracted. They may have difficulty organizing their private life and work.

Not all patients with ADHD need treatment with medication.

ADHD does not affect intelligence.

2. What you need to know before you or your child take Concerta

Do not take Concerta if you or your child:

• are allergic to methylphenidate or any of the other ingredients of this medicine (listed in section 6)
• have a thyroid problem
• have high eye pressure (glaucoma)
• have a tumor in the adrenal glands (pheochromocytoma)
• have an eating disorder, loss of appetite, or do not want to eat, such as in “anorexia nervosa”
• have very high blood pressure or narrowing of the blood vessels, which can cause pain in the arms and legs
• have had heart problems such as a heart attack, irregular heartbeat, chest pain, heart failure, heart disease, or a heart problem at birth
• have had a problem with the blood vessels in the brain such as a stroke, widening or weakening of part of a blood vessel (aneurysm), narrowing or blockage of the blood vessels, or inflammation of the blood vessels (vasculitis)
• are taking or have taken in the last 14 days a certain type of antidepressant (known as a monoamine oxidase inhibitor), see “Taking Concerta with other medicines”
• have mental health problems such as:

• a “psychopathic” or “borderline personality” disorder
• abnormal thoughts or visions or a disease called “schizophrenia”
• signs of a severe mood disorder such as:
• • suicidal thoughts
  • severe depression, feeling very sad, worthless, and desperate
  • mania, feeling exceptionally elated, more active than usual, and uninhibited

Do not take methylphenidate if you or your child have any of the above. If you are not sure, inform your doctor or pharmacist before you or your child take methylphenidate. This is because methylphenidate may worsen these problems.

Warnings and precautions

Talk to your doctor before starting to take Concerta if you or your child:

• have liver or kidney problems
• have problems swallowing or swallowing whole tablets
• have a narrowing or blockage in the digestive tract
• have had seizures (fits, convulsions, epilepsy) or any changes in the electroencephalogram (EEG, a brain study)
• have ever abused or been dependent on alcohol, prescription medicines, or drugs
• are female and have started having periods (see below the section on “Pregnancy and breastfeeding”)
• have difficulty controlling repetitive movements or sounds and words
• have high blood pressure
• have a heart problem not listed in the previous “Do not take” section
• have a mental health problem not listed in the previous “Do not take” section. Other mental health problems include:

• mood changes (from being manic to being depressed, known as “bipolar disorder”)
• feeling aggressive or hostile
• seeing, hearing, or feeling things that are not there (hallucinations)
• believing things that are not real (delusions)
• feeling strangely suspicious (paranoia)
• feeling agitated, anxious, or tense
• feeling depressed or guilty

Tell your doctor or pharmacist if you or your child have any of the above before starting treatment. This is because methylphenidate may worsen these problems. Your doctor will want to monitor how the medicines affect you or your child.

During treatment, children and adolescents may unexpectedly have prolonged erections. The erections can be painful and occur at any time. It is essential to contact the doctor immediately if the erection lasts more than 2 hours, especially if it is painful.

Checks that your doctor will make before you or your child start treatment with Concerta

To decide if methylphenidate is the right medicine for you or your child, your doctor will talk to you about:

• the medicines you or your child are taking
• if you or your child have a family history of sudden unexplained death
• other illnesses that you or your family (such as heart problems) may have
• how you or your child are feeling, if you or your child have mood swings, have unusual thoughts, or have had such feelings in the past
• if there have been cases of tics in your family (difficulty controlling repetitive movements or sounds and words)
• possible behavioral or mental health problems that you or your child or other family members have had. Your doctor will explain specifically if you or your child are at risk of mood changes (from being manic to being depressed, known as bipolar disorder). He/your doctor will check your or your child's mental health history and check if any family members have a history of suicide, bipolar disorder, or depression.

It is essential to provide all the information you can. This will help your doctor decide if methylphenidate is the right medicine for you or your child. Your doctor may decide that you or your child need other medical tests before starting to take this medicine. For adults starting to take Concerta, your doctor may refer you to a cardiologist.

Other medicines and Concerta

Tell your doctor if you or your child are taking, have recently taken, or might take any other medicines.

Do not take methylphenidate if you or your child:

• are taking a medicine called a “monoamine oxidase inhibitor” (MAOI) used for depression or have taken an MAOI in the last 14 days. Taking an MAOI with methylphenidate can cause a sudden increase in blood pressure (see “Do not take Concerta”).

Tell your doctor or pharmacist if you or your child are taking any of the following medicines for depression or anxiety:

• tricyclic antidepressant
• selective serotonin reuptake inhibitor (SSRI)
• serotonin and noradrenaline reuptake inhibitor (SNRI)

Taking methylphenidate with these types of medicines can cause a potentially life-threatening increase in “serotonin” in the brain (serotonin syndrome), which can cause confusion or restlessness, sweating, chills, muscle spasms, or rapid heartbeat. If you or your child experience these side effects, see a doctor immediately.

If you or your child are taking other medicines, methylphenidate may affect how they work or cause side effects. If you or your child are taking any of the following medicines, talk to your doctor or pharmacist before taking methylphenidate:

• medicines for severe mental health problems
• medicines for Parkinson's disease (such as levodopa)
• medicines for epilepsy
• medicines used to lower or increase blood pressure
• certain cough and cold remedies that contain medicines that can affect blood pressure. It is essential to talk to your pharmacist when buying any of these medicines
• medicines that thin the blood to prevent blood clots

If you are unsure whether any of the medicines you or your child are taking are included in the list above, talk to your doctor or pharmacist for advice before taking methylphenidate.

Tell your doctor or pharmacist if you or your child are using or have recently used any other medicines, including those bought without a prescription.

Before an operation

Tell your doctor if you or your child are going to have an operation. You should not take methylphenidate on the day of the operation with certain types of anesthetics, as it may cause a sudden increase in blood pressure during the procedure.

Drug tests

This medicine may give a positive result in drug tests, even in tests used in sports.

Concerta with alcohol

Do not drink alcohol while taking this medicine. Alcohol may worsen the side effects of this medicine. Remember that some foods and medicines contain alcohol.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, talk to your doctor before using this medicine.

Available data do not suggest an increased risk of total congenital anomalies, although a small increase in the risk of cardiac malformations during use in the first three months of pregnancy could not be ruled out. Your doctor will provide more information about this risk. Talk to your doctor or pharmacist before using methylphenidate if you or your daughter:

• are having sex. Your doctor will discuss contraception with you
• are pregnant or think you may be pregnant. Your doctor will decide whether you should use methylphenidate
• are breastfeeding or plan to breastfeed. Methylphenidate passes into breast milk. Therefore, your doctor will decide whether you or your daughter should breastfeed while using methylphenidate

Driving and using machines

You or your child may have dizziness, problems focusing, or blurred vision when taking methylphenidate. If this happens, it may be dangerous to perform certain activities such as driving, operating machinery, riding a bicycle or horse, or climbing trees.

Concerta contains lactose

This medicine contains lactose (a type of sugar). If your doctor has told you that you or your child have an intolerance to certain sugars, talk to them before taking this medicine.

Concerta contains sodium

This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially “sodium-free”.

3. How to take Concerta

How much to take

Follow the exact instructions for taking this medicine given by your doctor. If you are unsure, talk to your doctor or pharmacist again.

Your doctor will usually start treatment with a low dose and increase the daily dose by 18 mg no more than once a week if necessary.

The goal should be the lowest dose that is effective for you. Your doctor will decide the maximum daily dose for you or your child.

You or your child should take Concerta once a day in the morning with a glass of water. The tablet should be swallowed whole and not chewed, broken, or crushed. The tablet can be taken with or without food.

The tablet does not dissolve completely after all the medicine has been released, and sometimes the tablet may appear in the stool. This is normal.

Use in children from 6 years of age

• The recommended initial dose of Concerta is 18 mg once a day for children who are not currently taking methylphenidate or for children who are switching from another stimulant to methylphenidate.
• The maximum daily dose is 54 mg.

Use in adults

• The maximum daily dose is 72 mg in adults.

For adults who have taken Concerta before:

• If you have already taken Concerta as a child or adolescent, the same daily dose (mg/day) can be used; your doctor will regularly check if any adjustment is needed.
• Adult patients may need a higher daily dose, but the doctor will try to give you the lowest dose that is effective.

For adults who have not taken Concerta before:

• The recommended initial dose is 18 mg per day.

If you or your child do not feel better after 1 month of treatment

If you or your child do not feel better after 1 month of treatment, tell your doctor. Your doctor may decide that you or your child need a different treatment.

Incorrect use of Concerta

If Concerta is not used correctly, it can cause abnormal behavior. This can also mean that you or your child start to depend on the medicine. Tell your doctor if you or your child have ever abused or been dependent on alcohol, prescription medicines, or drugs.

This medicine is only for you or your child. Do not give this medicine to anyone else, even if they have similar symptoms.

If you or your child take more Concerta than you should

If you or your child take too many tablets, talk to a doctor or go to the nearest hospital emergency department immediately and tell them how many tablets were taken. Medical treatment may be necessary.

You can also contact the Toxicology Information Service, Telephone 91 5620420, stating the medicine and the amount taken. It is recommended to take the packaging and package leaflet of the medicine to the healthcare professional.

Signs of overdose may include: being sick, agitation, tremors, increased uncontrolled movements, muscle contractions, seizures (which can be followed by coma), feeling very happy, confusion, seeing, hearing, or feeling things that are not there (hallucinations), sweating, flushing, headache, high fever, changes in heartbeat (slow, fast, or irregular), high blood pressure, dilated pupils, and dryness of the nose and mouth.

If you or your child forget to take Concerta

Do not take a double dose to make up for forgotten doses. If you or your child forget a dose, wait and take the next dose at the scheduled time.

If you or your child stop taking Concerta

If you or your child suddenly stop taking this medicine, ADHD symptoms may return or unwanted effects such as depression may occur. Your doctor may want to gradually reduce the amount of medicine you or your child take each day before stopping it completely. Talk to your doctor before stopping treatment with Concerta.

What your doctor will do while you or your child are on treatment

Your doctor will perform some tests

• before you or your child start treatment to ensure that Concerta is safe and beneficial
• once treatment has started, at least every 6 months and even more often. They will also be performed when the dose is changed.
• these tests will include:

• appetite control
• height and weight measurement
• blood pressure and heart rate measurement
• evaluation of mood-related problems, mental state, or any other unusual feelings. Or if these have worsened while taking Concerta.

Long-term treatment

Concerta does not need to be taken indefinitely. If you or your child take Concerta for more than a year, your doctor should interrupt treatment for a short period, such as during school holidays. This allows your doctor to check if you or your child still need the medicine.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. Possible Adverse Effects

Like all medicines, this medicine can cause adverse effects, although not all people suffer from them. Although some people present adverse effects, most people are helped by methylphenidate. Your doctor will inform you about these adverse effects.

Some adverse effects can be serious. If you or your child have any of the following adverse effects, go to your doctor immediately:

Frequent (may affect up to 1 in 10 people)

• irregular heartbeats (palpitations)
• changes or alterations in mood or personality changes.

Uncommon (may affect up to 1 in 100 people)

• suicidal thoughts or feelings
• seeing, feeling, or hearing things that are not real, symptoms of psychosis
• uncontrolled speech and body movements (Tourette's syndrome)
• allergy signs such as rash, itching, or hives on the skin, swelling of the face, lips, tongue, or other parts of the body, shortness of breath, difficulty or problems breathing.

Rare (may affect up to 1 in 1,000 people)

• feeling exceptionally excited, more active than normal, and uninhibited (mania).

Very Rare (may affect up to 1 in 10,000 people)

• heart attack
• sudden death
• suicidal intention
• seizures (attacks, convulsions, epilepsy)
• skin peeling or red purpuric spots
• inflammation or blockage of the arteries in the brain
• temporary paralysis or movement and vision problems, speech difficulties (these signs may be related to problems with blood vessels in the brain)
• uncontrolled muscle spasms that affect the eyes, head, neck, body, and nervous system
• decrease in the number of blood cells (red blood cells, white blood cells, and platelets) that can cause a higher risk of infections and easier bleeding and bruising
• sudden increase in body temperature, very high blood pressure, and severe convulsions ("Neuroleptic Malignant Syndrome"). It is not entirely certain that this adverse effect is caused by methylphenidate or other medications taken in combination with methylphenidate.

Unknown frequency (frequency cannot be estimated from available data)

• unwanted recurring thoughts
• unexplained fainting, chest pain, shortness of breath (may be signs of heart problems)
• prolonged erections, sometimes painful, or increased number of erections.

If you or your child have any of the above adverse effects, go to your doctor immediately.

Other adverse effects are indicated below, and if they become severe, please inform your doctor or pharmacist:

Very Common (may affect more than 1 in 10 people)

• headache
• feeling of nervousness
• difficulty sleeping.

Common (may affect up to 1 in 10 people)

• joint pain
• blurred vision
• tension headache
• dry mouth, thirst
• problem staying asleep
• high temperature (fever)
• decreased sexual desire
• hair loss or decreased hair thickness (thinner hair)
• muscle tension, muscle cramps
• loss of appetite or decreased appetite
• inability to have or maintain an erection
• itching, rash, or red eruptions that itch (hives)
• excessive drowsiness or sleepiness, feeling tired
• excessive teeth grinding (bruxism)
• panic feeling
• tingling, itching, or numbness of the skin
• increased levels of alanine aminotransferase in blood (liver enzyme)
• cough, sore throat, and irritation of the throat or nose; upper respiratory tract infection; sinusitis
• high blood pressure, rapid heart rate (tachycardia)
• dizziness (vertigo), feeling of weakness, uncontrolled movements, abnormal activity
• aggression, agitation, anxiety, depression, irritability, tension, nervousness, and abnormal behavior
• stomach discomfort or indigestion, stomach pain, diarrhea, feeling nauseous, stomach upset, and vomiting
• excessive sweating
• weight loss.

Uncommon (may affect up to 1 in 100 people)

• dry eyes

• constipation
• chest discomfort
• blood in the urine
• apathy
• agitation or tremor
• increased need to urinate
• muscle pain, muscle spasms
• shortness of breath or chest pain
• feeling of heat
• increased liver test results (seen in a blood test)
• anger reaction (angry), restless or tearful, excessive awareness of the environment, sleep problems.

Rare (may affect up to 1 in 1,000 people)

• changes in sexual desire
• feeling disoriented or confused
• vision problems or double vision
• breast enlargement in men
• skin redness, increased redness of skin rashes
• obsessive-compulsive disorder (OCD) (includes irresistible urge to pull out body hair, having unwanted thoughts, feelings, images, or impulses in the mind (obsessive thoughts), performing repeated mental behaviors or rituals (compulsions)).

Very Rare (may affect up to 1 in 10,000 people)

• muscle cramps
• small red spots on the skin
• abnormal liver function, including sudden liver failure and coma
• changes in test results, including liver and blood tests
• abnormal thinking, lack of feelings or emotion
• feeling cold in arms and legs
• fingers and toes numb, tingling, and color change with cold (from white to blue then red) ("Raynaud's phenomenon").

Unknown frequency (frequency cannot be estimated from available data)

• migraine
• dilated pupils
• very high fever
• slow, rapid, or irregular heartbeats
• major epileptic seizure ("grand mal" convulsions)
• believing things that are not true
• severe stomach pain with discomfort and vomiting
• problems with blood vessels in the brain (stroke, cerebral arteritis, or cerebral occlusion)
• inability to control urination (incontinence)
• jaw muscle spasm that makes it difficult to open the mouth (trismus)
• stuttering
• nosebleed.

Effects on Growth

When used for more than a year, methylphenidate may reduce growth in some children. This affects less than 1 in 10 children.

• may prevent weight or height gain.
• your doctor will carefully check the height and weight of you or your child, as well as their diet.

Reporting of Adverse Effects

If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that is not listed in this leaflet. You can also report them directly through the Spanish Medicines Monitoring System for Human Use: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.

5. Storage of Concerta

Keep this medicine out of sight and reach of children.

Do not use this medicine after the expiration date shown on the packaging. The expiration date is the last day of the month indicated.

Keep the bottle tightly closed to protect it from moisture. Do not store above 30°C.

The package contains one or two silica gel bags. These bags are used to keep the tablets dry and should not be ingested.

Medicines should not be disposed of via wastewater or household waste. Deposit the packaging and unused medicines at the SIGRE collection point in the pharmacy. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.

6. Package Contents and Additional Information

Composition of Concerta

The active ingredient is methylphenidate hydrochloride

• Concerta contains 36 milligrams of methylphenidate hydrochloride.

The other ingredients are:

• Butylhydroxytoluene (E321), cellulose acetate, hypromellose (E464), concentrated phosphoric acid, poloxamer 188, polyethylene oxides 200K and 7000K, povidone K29-32, sodium chloride, stearic acid, succinic acid, black iron oxide (E172), yellow iron oxide (E172).
• Coating-film:hypromellose (E464), lactose monohydrate, titanium dioxide (E171), triacetin.
• Transparent coating:carnauba wax, hypromellose (E464), and macrogol 400.
• Printing ink:black iron oxide (E172), hypromellose (E464), and propylene glycol.

Appearance of the Product and Package Contents

Concerta is available in 4 doses: 18 milligrams, 27 milligrams, 36 milligrams, and 54 milligrams.

Each capsule-shaped tablet is individually marked for identification:

• 18 milligrams: yellow, with "alza 18" printed in black on one side
• 27 milligrams: gray, with "alza 27" printed in black on one side.
• 36 milligrams: white, with "alza 36" printed in black on one side.
• 54 milligrams: reddish-brown, with "alza 54" printed in black on one side.

The medicine is presented in bottles containing 28 or 30 prolonged-release tablets.

Only some pack sizes may be marketed.

Marketing Authorization Holder

Janssen-Cilag, S.A.

Paseo del Club Deportivo 1, Edificio 16

28223 Pozuelo de Alarcón (Madrid)

Spain

Manufacturer

JANSSEN PHARMACEUTICA N.V

Turnhoutseweg 30, 2340

Beerse, Belgium.

This medicine is authorized in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names:

Austria Concerta 18 mg, 36 mg & 54 mg Retardtabletten

Belgium Concerta 18 mg, 36 mg & 54 mg tabletten met verlengde afgifte

Bulgaria Concerta 18 mg ???????? ? ???????? ?????????????

Cyprus Concerta 18 mg, 36 mg, 54 mg Δισκ?ο παρατεταμ?νης αποδ?σμευσης

Czech Republic Concerta 18 mg, 36 mg, 54 mg tableta s prodlouženým uvolnováním

Denmark Concerta 18 mg, 36 mg, 54 mg Depottabletter

Estonia Concerta 18 mg, 36 mg, 54 mg toimeainet prolongeeritult vabastav tablett

Finland Concerta 18 mg, 36 mg, 54 mg depottabletit

France Concerta LP 18 mg, 36 mg, 54 mg comprimés à libération prolongée

Germany Concerta 18 mg, 36 mg, 54mg Retardtabletten

Greece Concerta 18 mg, 36 mg, 54 mg Δισκ?ο παρατεταμ?νης αποδ?σμευσης

Iceland Concerta 18 mg, 36 mg & 54 mg forðatöflur

Ireland Concerta XL 18 mg & 36 mg Prolonged-Release Tablets

Lithuania Concerta 18 mg, 36 mg, 54 mg pailginto atpalaidavimo tablete

Luxembourg Concerta 18 mg, 36 mg & 54 mg comprimés à libération prolongée

Malta Concerta 18 mg, 36 mg, 54 mg pilloli b’rilaxx imtawwal

Netherlands Concerta 18 mg, 36 mg & 54 mg tabletten met verlengde afgifte

Norway Concerta 18 mg, 36 mg & 54 mg depottabletter

Poland Concerta 18 mg, 36 mg Tabletka o przedluzonym uwalnianiu

Portugal Concerta 18 mg, 36 mg & 54 mg comprimidos de libertação prolongada

Romania Concerta 18 mg, 36 mg, 54 mg comprimat cu eliberare prelungita

Slovakia Concerta 18 mg, 36 mg, 54 mg Tableta s predlženým uvolnovaním

Slovenia Concerta 18 mg, 36 mg, 54 mg Tablete s podaljšanim sprošcanjem

Spain Concerta 18 mg, 36 mg & 54 mg comprimidos de liberación prolongada

Sweden Concerta 18 mg, 36 mg & 54 mg depottabletter

UK (Northern Ireland) Concerta XL 18mg, 36mg & 54mg Prolonged-Release Tablet

Date of the last revision of this leaflet:November 2024.

Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es).