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AMFEXA 10MG TABLET

Active substance(s): DEXAMFETAMINE SULFATE

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Package leaflet: Information for the patient
Amfexa 10 mg/20 mg tablets
dexamfetamine sulfate

This medicine is subject to additional monitoring. This will allow quick identification of new safety
information. You can help by reporting any side effects you may get. See the end of section 4 for how to
report side effects.
Read all of this leaflet carefully before your child starts taking this medicine because it contains
important information for you.





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

What is in this leaflet:
1. What Amfexa is and what it is used for
2. What you need to know before you use Amfexa
3. How to use Amfexa
4. Possible side effects
5. How to store Amfexa
6. Contents of the pack and other information
1. WHAT AMFEXA IS AND WHAT IT IS USED FOR
What Amfexa is
Amfexa tablets contain the active substance dexamfetamine sulfate.
Amfexa is a psychostimulant. It improves activity in parts of the brain. This medicine can help to improve
attention span, concentration, and reduce impulsive behaviour.
What it is used for
Amfexa is used to treat attention-deficit/hyperactivity disorder (ADHD).





It is used in children and adolescents aged 6-17 years.
It is not indicated in all children with ADHD.
It is used only after when another medicine called methylphenidate was not sufficiently effective.
It should be used as part of a treatment programme which typically includes psychological, educational and social measures.

Amfexa treatment must only be initiated by, and used under the supervision of a specialist in childhood or
adolescent behavioural disorders.
You must talk to a doctor if your child does not feel better or if they feel worse after a month. The doctor
may decide that a different treatment is needed.

2. WHAT YOU NEED TO KNOW BEFORE YOU USE AMFEXA
Do not use Amfexa if your child:

















is allergic (hypersensitive) to dexamfetamine or other amfetamine compounds or any of the other
ingredients of Amfexa (listed in section 6)
has a thyroid problem
has increased pressure in the eyes (glaucoma)
has a tumour of the adrenal gland (phaeochromocytoma)
has an eating problem, does not feel hungry or does not want to eat (e.g anorexia nervosa)
has very high blood pressure or narrowing of the blood vessels, which can cause pain in the arms
and legs
has advanced arteriosclerosis
has ever had heart problems - such as a heart attack, uneven heartbeat, pain and discomfort in the
chest, heart failure, heart disease, or was born with a heart problem
has had a problem with the blood vessels in the brain - such as a stroke, swelling and weakening of
part of a blood vessel (aneurysm), narrow or blocked blood vessels, or inflammation of the blood
vessels (vasculitis)
has mental health problems such as:
- a psychopathic or borderline personality disorder
- abnormal thoughts or visions or schizophrenia
- signs of a severe mood disorder like:
○ suicidal feelings
○ severe depression
○ mania
is currently taking or has taken within the last 14 days an antidepressant (known as a monoamine
oxidase inhibitor) – see the ‘Other medicines and Amfexa’ section below
has ever abused alcohol, prescription medicines, or street drugs
or anyone in your family has Tourette’s syndrome or other motor or verbal tics
has hard-to-control, repeated twitching of any parts of the body or repeats sounds and words
has porphyria.

Do not use this medicine if any of the above applies to your child. If you are not sure, talk to your doctor
or pharmacist before you use Amfexa. This is because this medicine can make these problems worse.
Warnings and precautions
Talk to your doctor or pharmacist before taking Amfexa if your child:








has a disease of the blood or liver, or kidney problems
is hyperexcitable or has an unstable personality
has had fits (seizures, convulsions, epilepsy) or any abnormal brain scans (EEGs)
is female and has started having periods (see the ‘Pregnancy and breast-feeding’ section below)
has high blood pressure
has a heart problem which is not in the ‘Do not use’ section above
has a mental health problem which is not in the ‘Do not use’ section above. This may include mood
swings, unusual aggression, hallucinations, delusions, paranoia, agitation and anxiety, feelings of
guilt or depression.

Tell your doctor or pharmacist if any of the above applies to your child before starting treatment. This is
because this medicine can make these problems worse. Your doctor will want to monitor how the medicine affects your child.
Checks that your doctor will make before Amfexa is used
These checks are to decide if this is the correct medicine for your child. Your doctor will talk to you
about:







any other medicines your child is 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
how your child is feeling, such as feeling high or low, having strange thoughts or if your child has
had any of these feelings in the past
whether there is a family history of ‘tics’ (hard-to-control, repeated twitching of any parts of the
body or repeating sounds and words)
any mental health or behaviour problems you or other family members have ever had.

Your doctor will discuss whether your child is at risk of having mood swings (from being manic to being
depressed - called ‘bipolar disorder’). They will check your child’s mental health history, and check if
any of your family has a history of suicide, bipolar disorder or depression.
It is important that you provide as much information as you can. This will help your doctor decide if Amfexa is the correct medicine for your child. Your doctor may decide that other medical tests are needed
before they start taking this medicine.
Effect on weight/growing
Amfexa may cause reduced weight in some children and adolescents.
• There may be lack of weight gain.
• Your doctor will carefully watch the height and weight of your child, as well as how well your
child is eating.
• If your child is not growing as expected, then your doctor may stop treatment with Amfexa for a
short time.
Having an operation
Tell your doctor if your child is going to have an operation. Amfexa should not be taken on the day of
surgery if a certain type of anaesthetic is used. This is because there is a chance of a sudden rise in blood
pressure during the operation.
Drug testing
This medicine may give a positive result when testing for drug use. Athletes must be aware that this medicinal product may cause a positive reaction to ‘anti-doping’ tests.
Children and adolescents
Amfexa is not for use as a treatment for ADHD in children under 6 years of age, and adults. It is not
known if it is safe or of benefit for these people.
Other medicines and Amfexa

Tell your doctor or pharmacist if your child is taking, has recently taken or might take any other
medicines, including medicines obtained without a prescription.
Monoamine oxidase inhibitors
Do not use this medicine if your child is taking a medicine called a ‘monoamine oxidase inhibitor’
(MAOI) used for depression, or has taken an MAOI in the last 14 days. Taking an MAOI with dexamfetamine may cause a sudden increase in blood pressure.
If your child is taking other medicines, this medicine may affect how well they work or may cause side
effects. If your child is taking any of the following medicines, check with your doctor or pharmacist before using Amfexa:
• other medicines for depression, e.g. tricyclic antidepressants and selective serotonin reuptake inhibitors
• medicines for severe mental health problems, e.g. phenothiazines and haloperidol
• medicines for epilepsy, e.g. anticonvulsants like phenobarbital, phenytoin, primidone, and
ethosuximide
• medicinal products that help to give up alcohol, e.g. disulfiram
• medicines used to reduce or increase blood pressure, e.g. guanethidine, clonidine, reserpine, or alpha-methyltyrosine, or beta-blockers such as propranolol
• some cough and cold remedies which contain medicines that can affect blood pressure
It is important to check with your pharmacist when you buy any of these products.
• medicines that thin the blood to prevent blood clots, e.g. coumarin anticoagulants
• any medicines that contain glutamic acid HCl, ascorbic acid, ammonium chloride, sodium acid
phosphate, sodium bicarbonate, acetazolamide, thiazides
• any of the following medicines: beta-blockers, antihistamines, lithium, noradrenaline, morphine,
and meperidine.
If you are in any doubt about whether any medicines your child is taking are included in the list above,
ask your doctor or pharmacist for advice before taking this medicine.
Amfexa with alcohol
Alcohol must not be consumed while taking this medicine. Remember that some foods and medicines
contain alcohol.
Pregnancy and breast-feeding
Amfexa may affect an unborn baby.
If your daughter is pregnant or breast-feeding, she may be pregnant or is planning to have a baby, ask
your doctor or pharmacist for advice before using this medicine.




Your doctor will discuss contraception.
If your daughter is pregnant she may have to stop taking this medicine.
It is possible that this medicine is passed into human breast milk. Therefore, your doctor will decide whether your daughter should stop breast-feeding or stop taking this medicine.

Driving and using machines

Your child may feel dizzy, have problems focussing, or have blurred vision when taking this medicine. If
so, it may be dangerous to do things such as drive, use machines, ride a bike or horse, or climb trees.
Amfexa contains isomalt (E953)
If you have been told by your doctor that your child cannot tolerate some sugars, talk to your doctor before using this medicinal product.

3. HOW TO TAKE AMFEXA
How much to take
Always use this medicine exactly as your doctor has told you. You should check with your doctor or
pharmacist if you are not sure.
The normal recommended dose is between 5 mg and 20 mg.
- Your doctor will usually start treatment with a low dose of one 5 mg tablet. This will be increased
gradually by one 5 mg tablet at weekly intervals, as required.
- The maximum daily dose is 20 mg (in rare cases, 40 mg may be needed).
- Your doctor will decide the need of giving Amfexa once or twice daily based on the course of symptoms at different times of the day.
How to take
The medicinal product is intended for oral use.
Your child should take Amfexa tablets with a drink of water, preferably with or immediately after meals.
Amfexa tablets should be taken at the same time in relation to the meals. The last dose should, in general,
not be given too late after lunch in order to prevent disturbances in falling asleep.
The tablets have a score line and can be divided, if needed. The score line is only there to help you break
the tablet if there is difficulty swallowing it whole and not to divide into equal doses. To split it, place the
tablet onto a hard surface with the cross-scored, smooth side downwards and then push carefully with
your index finger at the centre of its top side. The tablet then breaks into four parts.
If your child does not feel better, tell your doctor. They may decide a different treatment is needed.
Long-term treatment
Your doctor will decide how long the treatment is given. If your child takes this medicine for more than a
year, your doctor should stop treatment for a short time, e.g. during a school holiday. This will show if the
medicine is still needed.

Not using Amfexa properly
If Amfexa is not used properly, it may cause abnormal behaviour. It may also mean that your child starts
to depend on the medicine. Tell your doctor if your child has ever abused or been dependent on alcohol,
prescription medicines or street drugs.
This medicine is only for your child. Do not give this medicine to anyone else, even if their symptoms
seem similar.
If your child takes more Amfexa than they should
Talk to a doctor or call an ambulance straight away. Tell them how much has been taken. Show the package or this leaflet to the doctor. Over dosage of these tablets can be very serious.
Signs of overdose may include: excitement, hallucinations, convulsions leading to coma, irregular and
rapid heartbeat, and reduced breathing.
If your child forgets to take Amfexa
Do not use a double dose to make up for a forgotten dose. If your child forgets a dose, wait until it is time
for the next dose.
If your child stops taking Amfexa
If your child suddenly stops taking this medicine, this can lead to extreme tiredness, depression, mood
disorders, agitation, sleep disturbances, increased appetite, or involuntary movements. Your doctor may
want to gradually reduce the amount of medicine taken each day, before stopping it completely. Talk to
your doctor before stopping Amfexa.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
4. POSSIBLE SIDE EFFECTS
Like all medicines, this medicine can cause side effects, but not everybody gets them. Your doctor will
talk to you about these side effects.
Very common: may affect more than 1 in 10 people
• decreased appetite, reduced weight gain and weight loss during prolonged use in children
• difficulty in sleeping
• nervousness
Common: may affect up to 1 in 10 people
• irregular or increased heartbeat, a more noticeable heartbeat
• abdominal pain and/or cramps, nausea, vomiting, dry mouth
These effects usually occur at the beginning of treatment and may be alleviated by taking the medicine with meals.
• changes in blood pressure and heart rate (usually increases)
• joint pain
• A feeling of dizziness or “spinning”, jerky or involuntary movements, headache, hyperactivity
• abnormal behaviour, aggression, excitation, anorexia, anxiety, depression, irritability

Rare: may affect up to 1 in 1,000 people
• angina pectoris
• difficulties in visual sharpening and focus, blurred vision, dilation of the pupils.
• reduced height increase during prolonged use in children
• fatigue
• rash, hives
Very rare: may affect up to 1 in 10,000 people
• reduction in red blood cells which can make the skin pale and cause weakness or breathlessness,
changes in blood cell counts (leukopenia, thrombocytopenia, thrombocytopenic purpura)
• cardiac arrest
• Tourette’s syndrome
• abnormal liver function ranging from hepatic enzyme elevations to hepatic coma
• muscle cramps
• convulsions, involuntary movements (choreoathetoid movements), bleeding inside the skull (intracranial haemorrhage)
• hallucinations, psychosis/psychotic reactions, suicidal behaviour or suicide, tics, worsening of preexisting tics
• itchy red skin lesions (erythema multiforme) or scaly skin patches (exfoliative dermatitis), recurring rash, which happens in the same place each time the medicine is taken (fixed drug eruption)
• inflammation of the blood vessels of the spinal cord and brain (cerebral vasculitis) and/or occlusion
Not known: frequency cannot be estimated from the available data
• heart muscle disease (cardiomyopathy), heart attack
• inflammation of parts of the large intestine when the blow flow is reduced (ischaemic colitis), diarrhoea
• chest pain, growth retardation during prolonged use, increased body temperature, allergic reactions
including serious allergic reaction which causes swelling of the face or throat (angioedema) and serious allergic reaction which causes difficulty in breathing or dizziness (anaphylaxis), sudden death
• disturbance of the acid-base balance of the body (acidosis)
• abnormal muscle breakdown which can lead to kidney problems (rhabdomyolysis)
• difficulty in controlling movements (ataxia), dizziness, abnormal or impaired sense of taste, concentration difficulties, hyperreflexia, stroke, shaking (tremor)
• confusion, dependence, dysphoria, emotional instability, euphoria, impaired cognitive test performance, altered libido, night terrors, obsessive-compulsive behaviour, panic states, paranoia, restlessness
• renal damage
• impotence
• sweating, hair loss
• circulatory failure
Reporting of side effects
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 the national system listed in the Yellow
Card Scheme at www.mhra.gov.uk/yellowcard.
By reporting side effects you can help provide more information on the safety of this medicine.

5. HOW TO STORE AMFEXA
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 blister and the box after “EXP”. The
expiry date refers to the last day of that month.
Do not store above 30 °C.
Store in the original package in order to protect from moisture.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw
away medicines you no longer use. These measures will help to protect the environment.
6. CONTENTS OF THE PACK AND OTHER INFORMATION
What Amfexa 10 mg/20 mg contains:
-

The active substance is dexamfetamine sulfate
Amfexa 10 mg:
One tablet contains 10 mg dexamfetamine sulfate
Amfexa 20 mg:
One tablet contains 20 mg dexamfetamine sulfate

-

The other ingredients are:
isomalt (E953)
magnesium stearate

What Amfexa looks like and the contents of the pack:
Amfexa 10 mg tablets
White, round, cloverleaf-shaped tablets with a notched, cross-scored line on the top side and a crossscored line embossed with ”M” on each quarter on the rear side.
The score line is only to facilitate breaking for ease of swallowing and not to divide into equal doses.
Pack sizes: 20, 30 or 50 tablets
Amfexa 20 mg tablets
White, round, cloverleaf-shaped tablets with a notched, cross-scored line on the top side and a crossscored line embossed with ”L” on each quarter on the rear side.
The score line is only to facilitate breaking for ease of swallowing and not to divide into equal doses.
Pack sizes: 20 or 30 tablets
Boxes containing tablets packed in blisters made of PVC/PVdC aluminium foil
Not all pack sizes may be marketed.

Marketing authorisation holder and manufacturer
MEDICE Arzneimittel Pütter GmbH & Co. KG
Kuhloweg 37
58638 Iserlohn
Germany
This package leaflet was last revised in {07/2016}

This package leaflet is also available in formats appropriate for the blind and partially sighted.

Version 0002

1.3.1.3 Package Leaflet en Page 9

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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