This medicine is used to treat ADHD

• The full name for ADHD is ‘Attention Deficit Hyperactivity Disorder’.
• The medicine helps with your brain activity. It can help improve your attention, help you concentrate, and make you less impulsive.
• You need to have other help for ADHD as well as this medicine.

Before you take this medicine, talk to your doctor if you:

• have mental health problems
• have a problem with your heart or blood circulation
• have serious problems with the blood vessels in your brain such as a stroke

While taking this medicine:

• See your doctor regularly. This is because your doctor will want to check how the medicine is working.
• Do not stop taking the medicine without first talking to your doctor.
• Your doctor may stop your medicine to see if it is still needed, if you take it for more than a year.
• The most common side effects in children and young people are:
  headache, stomach ache, not feeling hungry, feeling or being sick, feeling sleepy, increased blood pressure, increased heart rate (pulse).
• The most common side effects in adults are:
  feeling sick, dry mouth, headache, not feeling hungry, not being able to sleep, increased blood pressure, increased heart rate (pulse).

Talk to your doctor straight away if any of the following happen:

• your mood and how you feel changes
• you feel any problems with your heart e.g. a fast or unusual heartbeat rhythm

The rest of this leaflet includes more detail and other important information on the safe and effective use of this medicine.

• Keep this leaflet. 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 only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
• If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

Sections 1 to 6 are for parents and carers (sometimes called ‘your guardians’).

The last section is a special section for a child or young person to read. However, all sections are written as though the child or young person taking the medicine is reading them.

1. What Strattera is and what it is used for
2. What you need to know before you take Strattera
3. How to take Strattera
4. Possible side effects
5. How to store Strattera
6. Contents of the pack and other information

Strattera contains atomoxetine and is used to treat attention-deficit and hyperactivity disorder (ADHD).
It is used

• in children over six years of age
• in young people
• in adults

It is used only as a part of the total treatment of the disease which also requires treatments which do not involve medicines, such as counselling and behavioural therapy.

It is not for use as a treatment for ADHD in children under 6 years of age as it is not known if the drug works or is safe in these people.

In adults, Strattera is used to treat ADHD when the symptoms are very troublesome and affect your work or social life and when you have had symptoms of the disease as a child.

Strattera increases the amount of noradrenaline in the brain. This is a chemical that is produced naturally, and increases attention and decreases impulsiveness and hyperactivity in patients with ADHD. This medicine has been prescribed to help control the symptoms of ADHD. This medicine is not a stimulant and is therefore not addictive.

It may take a few weeks after you start the medicine for your symptoms to fully improve.

Children and young people with ADHD find it:

• hard to sit still and
• hard to concentrate.

It is not their fault that they cannot do these things. Many children and young people struggle to do these things. However, with ADHD this can cause problems with everyday life. Children and young people with ADHD may have difficulty learning and doing homework. They find it hard to behave well at home, at school or in other places. ADHD does not affect the intelligence of a child or young person.

Adults with ADHD find it difficult to do all the things that children find difficult however this may mean they have problems with:

• work
• relationships
• low self esteem
• education

• are allergic to atomoxetine or any of the other ingredients of this medicine (listed in section 6)
• took a medicine known as a monoamine oxidase inhibitor (MAOI), for example phenelzine, in the last two weeks. An MAOI is sometimes used for depression and other mental-health problems; taking Strattera with an MAOI could cause serious side effects or be life-threatening. You also need to wait at least 14 days after you stop taking Strattera before you take an MAOI
• have an eye disease called narrow-angle glaucoma (increased pressure in your eye)
• have serious problems with your heart which may be affected by an increase in heart rate and/or blood pressure, as this may be an effect of Strattera
• have serious problems with the blood vessels in your brain - such as a stroke, swelling and weakening of part of a blood vessel (aneurysm) or narrow or blocked blood vessels
• have a tumour of your adrenal gland (phaeochromocytoma)

Do not take Strattera if any of the above applies to you. If you are not sure, talk to your doctor or pharmacist before you take Strattera. This is because Strattera can make these problems worse.

Both adult and children should be aware of the following warnings and precautions. Talk to your doctor or pharmacist before taking Strattera if you have:

• thoughts about killing yourself or trying to kill yourself.
• problems with your heart (including heart defects) or an increased heartbeat. Strattera can increase your heart rate (pulse). Sudden death has been reported in patients with heart defects.
• high blood pressure. Strattera can increase blood pressure.
• low blood pressure. Strattera can cause dizziness or fainting in people with low blood pressure.
• problems with sudden changes in your blood pressure or your heart rate.
• cardiovascular disease or past medical history of stroke.
• liver problems. You may need a lower dose.
• psychotic symptoms including hallucinations (hearing voices or seeing things which are not there), believing things that are not true or being suspicious.
• mania (feeling elated or over-excited, which causes unusual behaviour) and agitation. aggressive feelings.
• unfriendly and angry (hostility) feelings.
• a history of epilepsy or have had seizures for any other reason. Strattera might lead to an increase in seizure frequency.
• different moods than usual (mood swings) or feel very unhappy.
• hard-to-control, repeated twitching of any parts of the body or you repeat sounds and words.

Tell your doctor or pharmacist if any of the above applies to you before starting treatment. This is because Strattera can make these problems worse. Your doctor will want to monitor how the medicine affects you.

These checks are to decide if Strattera is the correct medicine for you.

Your doctor will measure your

• blood pressure and your heart rate (pulse) before and during the time you take Strattera
• your height and weight if you are a child or teenager during the time you take Strattera

Your doctor will talk to you about:

• any other medicines you are taking
• whether there is any family history of sudden unexplained death
• any other medical problems (such as heart problems) you or your family may have

It is important that you provide as much information as you can. This will help your doctor decide if Strattera is the correct medicine for you. Your doctor may decide that other medical tests are needed before you start taking this medicine.

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

This includes non-prescription medicines. Your doctor will decide if you can take Strattera with your other medicines and in some cases your doctor may need to adjust your dose or increase your dose much more slowly.

Do not take Strattera with medicines called MAOIs (monoamine oxidase inhibitors) used for depression. See section 2. “Do not take Strattera”.

If you are taking other medicines, Strattera may affect how well they work or may cause side effects. If you are taking any of the following medicines, check with your doctor or pharmacist before taking Strattera:

• medicines that increase blood pressure or are used to control blood pressure
• medicines such as antidepressants, for example imipramine, venlafaxine, mirtazapine, fluoxetine and paroxetine
  • some cough and cold remedies which contain medicines that can affect blood pressure.
    It is important to check with your pharmacist when you get any of these products
• some medicines used to treat mental health conditions
• medicines that are known to increase the risk of seizures
• some medicines that cause Strattera to stay in the body for longer than normal (such as quinidine and terbinafine)
• salbutamol (a medicine to treat asthma) when taken by mouth or injected may make you feel as if your heart is racing, but this will not make your asthma worse

The medicines below may lead to an increased risk of an abnormal rhythm of the heart when taken with Strattera:

• medicines used to control the rhythm of the heart,
• medicines which change the concentration of salts in the blood,
• medicines for malaria prevention and treatment,
• some antibiotic medicines (such as erythromycin and moxifloxacin).

If you are not sure about whether any medicines you are taking are included in the list above, ask your doctor or pharmacist before taking Strattera.

It is not known if this medicine can affect an unborn baby or pass into breast milk.

• This medicine should not be used during pregnancy, unless your doctor has advised you to do so.
• You should either avoid taking this medicine if you are breastfeeding or discontinue breastfeeding.

If you are:

• pregnant or breast feeding,
• thinking that you may be pregnant or are planning to have a baby,
• planning to breastfeed your baby,

ask your doctor or pharmacist for advice before taking this medicine.

You may feel tired, sleepy or dizzy after taking Strattera. You should be careful if you are driving a car or operating machinery until you know how Strattera affects you. If you feel tired, sleepy or dizzy you should not drive or operate machinery.

This oral solution can irritate the eye. If the oral solution comes into contact with the eye, the affected eye should be flushed immediately with water, and medical advice obtained. Hands and any other part of the body that may have come into contact with the oral solution should also be washed as soon as possible.

This medicine contains 32.97 mg sorbitol in each mL. Sorbitol is a source of fructose. If your doctor has told you that you (or your child) have an intolerance to some sugars or if you have been diagnosed with hereditary fructose intolerance (HFI), a rare genetic disorder in which a person cannot break down fructose, talk to your doctor before you (or your child) take or receive this medicine.

This medicine contains 2.64 mg of sodium (main component of cooking/table salt) in each mL. This is equivalent to 3.3 % of the recommended maximum daily dietary intake of sodium for an adult.

This medicine contains 0.8 mg of sodium benzoate in each mL.

This medicine contains 9.8 mg of propylene glycol in each mL.

If you are a child or teenager (6 years or older):

Your doctor will tell you how much Strattera you should take and will calculate this according to your weight. He/she will normally start you on a lower dose before increasing the amount of Strattera you need to take according to your body weight.

• Body weight up to 70 kg: a starting total daily dose of 0.5 mg per kg of body weight for a minimum of 7 days. Your doctor may then decide to increase this to the usual maintenance dose of about 1.2 mg per kg of body weight daily.
• Body weight over 70 kg: a starting total daily dose of 40 mg for a minimum of 7 days. Your doctor may then decide to increase this to the usual maintenance dose of 80 mg daily. The maximum daily dose your doctor will prescribe is 100 mg.

• Strattera should be started at a total daily dose of 40 mg for a minimum of 7 days. Your doctor may then decide to increase this to the usual maintenance dose of 80 mg-100 mg daily. The maximum daily dose your doctor will prescribe is 100 mg.

If you have problems with your liver your doctor may prescribe a lower dose.

If you take more Strattera than you should contact your doctor or the nearest hospital casualty department immediately and tell them how much medicine you have taken. The most commonly reported symptoms accompanying overdoses are gastrointestinal symptoms, sleepiness, dizziness, tremor, and abnormal behaviour.

If you miss a dose, you should take it as soon as possible, but you should not take more than your total daily dose in any 24-hour period. Do not take a double dose to make up for a forgotten dose.

If you stop taking Strattera there are usually no side effects but your ADHD symptoms may return. You should talk to your doctor first before you stop treatment.

Your doctor will do some tests

• before you start - to make sure that Strattera is safe and will be of benefit.
• after you start - they will be done at least every 6 months, but possibly more often.

They will also be done when the dose is changed. These tests will include:

• measuring height and weight in children and young people
• measuring blood pressure and heart rate
• checking whether you have any problems or if side effects have got worse while taking Strattera

Strattera does not need to be taken for ever. If you take Strattera for more than a year, your doctor will review your treatment, to see if the medicine is still needed.

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

• thinking about or feeling like killing yourself (may affect up to 1 in 100 people)
• mood swings or mood changes (may affect up to 1 in 10 people)

Adults have a reduced risk (may affect up to 1 in 1,000 people) of side effects such as:

• seizures
• psychotic symptoms including hallucinations (hearing voices or seeing things which are not there), believing things that are not true or being suspicious

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

• liver injury

• dark urine
• yellow skin or yellow eyes
• tummy pain which is sore when you press it (tenderness) on the right side just below your ribs
• a feeling of sickness (nausea) that is unexplained
• tiredness
• itching
• feeling that you are coming down with flu.

Very common side effects (may affect more than 1 in 10 people)

CHILDREN and YOUNG PEOPLE over 6 years

• headache
• pain in the stomach
• decreased appetite (not feeling hungry)
• feeling or being sick
• sleepiness
• increased blood pressure
• increased heart rate (pulse)

These effects may disappear after a while in most patients.

ADULTS

• feeling sick
• dry mouth
• headache
• decreased appetite (not feeling hungry)
• problems getting to sleep, staying asleep and waking early
• increased blood pressure
• increased heart rate (pulse)

Common side effects (may affect up to 1 in 10 people)

CHILDREN and YOUNG PEOPLE over 6 years

• being irritable or agitated
• problems sleeping including waking early
• depression
• feeling sad or hopeless
• feeling anxious
• tics
• large pupils (the dark centre of the eye)
• dizziness
• constipation
• loss of appetite
• upset stomach, indigestion
• swollen, reddened and itchy skin
• rash
• feeling lazy (lethargy)
• chest pain
• tiredness
• weight loss

ADULTS

• feeling agitated
• decreased interest in sex
• sleep disturbance
• depression
• feeling sad or hopeless
• feeling anxious
• dizziness
• an abnormal taste or change in taste that will not go away
• tremor
• tingling or numbness in the hands or feet
• sleepiness, drowsy, feeling tired
• constipation
• stomach ache
• indigestion
• wind (flatulence)
• being sick
• hot flush or flushing
• feeling or having a very fast heartbeat
• swollen, reddened and itchy skin
• increased sweating
• rash
• problems going to the toilet such as not be able to urinate, frequent or hesitant urinating, pain on urinating
• inflammation of the prostate gland (prostatitis)
• groin pain in men
• failure to obtain an erection
• retarded orgasm
• difficulty maintaining an erection
• menstrual cramps
• lack of strength or energy
• tiredness
• feeling lazy (lethargy)
• chills
• feeling, irritable, jittery
• feeling thirsty
• weight loss

Uncommon side effects (may affect up to 1 in 100 people)

CHILDREN and YOUNG PEOPLE over 6 years

• fainting
• tremor
• migraine
• blurred vision
• abnormal skin sensation, such as burning, prickling, itching, or tingling
• tingling or numbness in the hands or feet
• seizure (fits)
• feeling or having a very fast heartbeat (QT prolongation)
• shortness of breath
• increased sweating
• itchy skin
• lack of strength or energy

ADULTS

• restlessness
• tics
• fainting
• migraine
• blurred vision
• heart rhythm abnormal (QT prolongation)
• feeling cold in fingers and toes
• chest pain
• shortness of breath
• raised red itchy rashes (hives)
• muscle spasms
• an urge to urinate
• abnormal or absence of orgasm
• irregular menstruation
• ejaculation failure

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

CHILDREN and YOUNG PEOPLE over 6 years

• poor blood circulation which makes toes and fingers numb and pale (Raynaud’s disease)
• problems going to the toilet such as frequent or hesitant urinating, pain on urinating
• prolonged and painful erections
• groin pain in males

ADULTS

• poor blood circulation which makes toes and fingers numb and pale (Raynaud’s disease)
• prolonged and painful erections

Some children experience reduced growth (weight and height) when they start taking Strattera. However, with long-term treatment, children recover to the weight and height for their age range. Your doctor will watch your child’s height and weight over time. If your child is not growing or gaining weight as expected, your doctor may change your child’s dose or decide to stop Strattera temporarily.

If you get 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 Ireland: via

or the United Kingdom (Great Britain and Northern Ireland):

or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

• The active substance is atomoxetine hydrochloride. Each mL of oral solution contains atomoxetine hydrochloride equivalent to 4 mg of atomoxetine.
• The other ingredients are sodium benzoate (E211), sodium dihydrogen phosphate dihydrate, phosphoric acid, liquid sorbitol (crystallising) E420, xylitol, artificial raspberry flavouring (containing propylene glycol E1520), sucralose, sodium hydroxide, purified water.

Oral solution, 4 mg/mL (clear colourless)

Strattera oral solution is available in a bottle with a child resistant cap containing 100 mL of solution.

The pack also includes a dosing device consisting of a 10 mL oral syringe marked in 1 mL increments and a press-in-bottle adaptor.

Strattera oral solution is available in a pack containing one bottle and in a multipack of three bottles.

Not all pack sizes may be marketed.

The marketing authorisation holder is:

The manufacturer is:

Strattera is a trademark of Eli Lilly and Company Limited.

This medicinal product is authorised in the Member States of the EEA under the following names:

Austria, Denmark, Germany, Hungary, Iceland, the Republic of Ireland, Italy, Malta, Norway, Portugal, Romania, Slovenia, Spain, Sweden and the UK: Strattera.