Medine.co.uk

Out of date information, search another

Risperidone 1 Mg Orodispersible Tablets

Out of date information, search another
Informations for option: Risperidone 1 Mg Orodispersible Tablets, show other option
Document: document 7 change

Package Leaflet: Information for the User

Risperidone 1 mg Orodispersible Tablets

Risperidone

Read all of this leaflet carefully before you start using 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. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.

■    If any of the side effects gets serious or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

In this leaflet:

1.    What Risperidone is and what it is used for

2.    Before you take Risperidone

3.    How to take Risperidone

4.    Possible side effects

5.    How to store Risperidone

6.    Further information

1.    What Risperidone is and what it is used for

Risperidone belongs to a group of medicines called antipsychotics.

Risperidone is used:

■    to treat schizophrenia (a severe mental illness characterised by symptoms such as delusional ideas, perceiving things that are not there (hallucinations) and a gradual change of personality).

■    to keep schizophrenia under control after the previous symptoms have declined, to prevent the illness from returning in its full intensity.

2.    Before You Take Risperidone

Do not take Risperidone

■    if you are allergic (hypersensitive) to risperidone or any of the other ingredients of Risperidone tablets. An allergic reaction may manifest as rash, pruritus, oedema of the face and lips or dyspnoea.

■    if you have an abnormally high concentration of the hormone prolactin in the blood.

Take special care with Risperidone

Tell your doctor if you suffer from the following conditions:

■    heart or vascular disease (e.g. low blood pressure)

■    Parkinson's disease

   dementia or you have previously had a stroke or a disorder of blood supply to the brain (because treatment with Risperidone can cause impaired cerebral blood flow possibly leading to stroke, particularly in elderly patients)

   Lewy body dementia (a special form of dementia)

   epilepsy

■    liver or kidney disease. Your treatment may need to be adjusted (see section 3)

■    diabetes mellitus

■    breast cancer (and other specific tumors which can be correlated to the hormone prolactin, e.g. hypophysal prolactinoma)

Tell your doctor immediately if you experience:

   involuntary rhythmic movements of the tongue, mouth and facial muscles

■    fever, severe muscular stiffness, sweating or a lowered level of consciousness

   signs and symptoms such as sudden weakness, numbness in the face, arms or legs, particularly on one side, or indistinct speech.

If you are of an advanced age:

In elderly people, dizziness, excessively low blood pressure and injury as a result of a tendency to fall occurs more often than in younger people.

If signs such as agitation, restlessness and aggressiveness are exacerbated: Antipsychotics can sometimes cause this, in which case a reduction of the dose or discontinuation of treatment may be necessary.

Please also tell your doctor if you have a factor increasing susceptibility to cardiovascular diseases, such as high blood pressure, diabetes, cardiac dysfunction called atrial fibrillation or if you smoke.

Your doctor will decide whether you can take Risperidone tablets and if the dosage should be adjusted.

Be cautious taking Risperidone if you are exposed to temperature extremes, because abnormally changes in body temperature can occur.

Avoid dehydration. Refrain from excessive eating to avoid weight gain during Risperidone treatment.

Using other medicines

Please tell your doctor or pharmacist, if you are taking or have recently taken any other medicines, including medicines or herbal and natural products obtained without a prescription.

Some medicines can cause problems if you take them with Risperidone. These include:

■    medicines acting upon the central nervous system (e.g. levodopa, used to treat Parkinson's disease): risperidone may weaken the effect of levodopa

   opiates (used to treat severe pain), antihistamines (used to treat allergies) and benzodiazepines (tranquilizing medicines): their effect is increased by risperidone

■    other antipsychotic medicnes (used to treat psychiatric disorders), lithium and antidepressants (used to treat depressions), medicines to treat Parkinson's disease and other medicinal products with a specific effect on the central nervous system: the risk that movement disturbances (tardive dyskinesia) occur as side effect is increased

■    neuroleptics (used to treat psychiatric disorders), antiarrhythmics class IA or III (used to treat heart disease), antibiotics (used to treat bacterial infections), medicines to treat malaria, antihistamines (used to treat allergies) and antidepressants (used to treat depressions): cardiac disorders may occur

■    certain diuretics (like chlorothiazide and furosemide), used to treat swellings (oedema) caused by water retention in the body: the body may lose to much water and minerals (sodium, chloride) and especially with furosemide when used in elderly patients with dementia cardiac disorders may occur. Thus concomitant use of furosemide with Risperidone is not recommended

■    certain blood pressure lowering medicines, e.g. phenoxybenzamine, labetalol, methyldopa, reserpine: risperidone can increase their effect

■    guanethidine, used to treat high blood pressure: risperidone blockes the effect

■    carbamazepine, phenytoin and phenobarbital (used to treat epilepsy), barbiturates (used for sedation), rifampicin (used to treat tuberculosis), the herbal remedy St. John's wort (Hypericum perforatum, used to treat depressive mood changes): they may weaken the effect of risperidone

■    antacida (used to treat stomach problems, e.g. heartburn): they may reduce the amount of Risperidone which is taken up by the body

   medicines which may increase the concentration of Risperidone in the blood so that your doctor might need to adjust the dose of Risperidone:

■    phenothiazines, used to treat psychiatric disorders

■    fluoxetine, paroxetine and tricyclic antidepressants, used to treat depressive conditions

   quinidine, used to treat heart disease

■    terbinafine, used to treat certain fungal infections

■    beta-blockers, used to treat high blood pressure

■    cimetidine and ranitidine, used to treat certain stomach problems

Using Risperidone with food and drink

The tablets can be taken with or without meals. Your mouth should be empty before taking the tablet. Abundant use of alcohol should be avoided during therapy with Risperidone since concomitant use may cause somnolence.

Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking any medicine.

Insufficient information is known about the use of risperidone during pregnancy in humans to assess the possible harmfulness. Long term use until birth can result in movement disorders and withdrawal symptoms in the newborn child. Risperidone may only be used during pregnancy if your doctor has carefully weighed up the benefits against the risks.

If you are pregnant or are planning to become pregnant, discuss with your doctor who will decide whether you can use Risperidone .

Risperidone passes into the breast milk in small quantities. Your doctor will carefully weigh up the benefits of breast feeding against the possible risks to the infant.

Driving and using machines

Risperidone therapy may impair alertness and affect the ability to drive or use machines. It is recommended to avoid driving and using machines requiring precision until the doctor has ensured that Risperidone does not impair your attention.

Important information about some of the ingredients of Risperidone

Risperidone orodispersible tablets contain aspartame (E951) which is a source of phenylalanine. Aspartame may be harmful for people with phenylketonuria.

3. How to take Risperidone

Risperidone orodispersible tablets are fragile. They should not be pushed through the foil in the blister pack as this will cause damage to the tablet. Remove a tablet from the package as follows:

1.    Hold the blister strip at the edges and separate one blister cell from the rest of the strip by gently tearing along the perforations around it.

2.    Pull up the edge of the foil and peel foil off completely.

3.    Tip the tablet out onto your hand.

4.    Put the tablet on the tongue as soon as it is removed from the packaging.

In a few seconds it begins disintegrating in the mouth and subsequently can be swallowed with or without water. The mouth should be empty before placing the tablet on the tongue.

Your doctor prescribes the correct dose and duration of treatment. These are individual and the doctor checks and adjusts the dosage until a dose suitable for you is achieved.

Spain

UK


Risperidon Krka 1 mg Orodispersible Tablets Risperidone 1 mg Orodispersible Tablets


Always take Risperidone exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

Important - Never take more than 16 mg per day.

Treatment of psychosis in adults and adolescents over 15 years of age:

Treatment is started gradually, e.g. 2 mg on the first day and 4 mg on the second day.

The daily dose can be taken in one dose or divided into two subdoses, one taken in the morning and another one in the evening. However, your doctor may recommend to increase the dose more slowly.

Thereafter, the dosage may remain the same or it can be adjusted, if necessary. The usual dose is 4-6 mg daily, but a dose less than 4 mg may be adequate for some patients.

Children and adolescents

Use of the product is not recommended for children and adolescents below the age of 15 years due to lacking experience.

Elderly patients

The recommended starting dose is 0.5 mg twice daily.

This dose can be adjusted, in steps of 0.5 mg twice daily, to a dose of 1 to 2 mg twice daily. Caution should be exercised because little experience has been acquired in the treatment of elderly patients.

Patients with cardiovascular disease

The doctor will prescribe the dosage which is appropriate for you. Dependent on the kind of disease and its severity the dosage can be lower as described above.

Patients with impaired liver or kidney function

The doctor will prescribe the dosage which is appropriate for you. Dependent on the kind of impairment and its severity the dosage can be as described above or only half of that.

Follow carefully the instructions from your doctor and do not change the dosage or discontinue the medicine without discussing with your doctor first.

Tell your doctor or pharmacist if you feel that the efficacy of Risperidone tablets is too strong or too weak.

If you take more Risperidone than you should

If you have taken too much of Risperidione, contact your doctor or a hospital straight away. Signs of an overdose needing medical care straight away are: fatigue, accelerated heart beat (tachycardia), low blood pressure (hypotension) and extrapyramidal symptoms like tremor, muscular stiffness, increased salivation, slowness of movements, restless legs and sudden muscular contractions.

If you forget to take Risperidone

Skip the forgotten dose and continue taking the medicine normally as instructed by the doctor.

If you stop taking Risperidone

Do not stop treatment without talking to your doctor first because abrupt stopping of therapy can cause so called withdrawal symptoms such as nausea, vomiting, sweating and insomnia. Therefore therapy needs to be discontinued by slowly reducing the dose of Risperidone over a certain period of time, exactly according to your doctor's recommendations.

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

4. Possible Side Effects

Like all medicines, Risperidone tablets can cause side effects, although not everybody gets them.

Common (in more than 1 in 100, but in less than 1 in 10 patients)

Uncommon (in more than 1 in 1,000, but in less than 1 in 100 patients)

Rare (in more than 1 in 10,000, but in less than 1 in 1,000 patients)

Very rare (in less than 1 in 10,000 patients)

Blood

Very rare: slight decrease in the amount of certain blood cells (neutrophils and thrombocytes)

Endocrine disorders:

Uncommon: elevated blood levels of the hormone prolactin leading to abnormal milk discharge from the breasts, disturbances of the menstrual cycle and even absence of menstruation.

Rare: enlargement of breasts in men

Metabolism

Very rare: high blood sugar (hyperglycaemia), exacerbation of preexisting diabetes

Mental disorders

Common: agitation, anxiety

Nervous system

Common: sleeplessness, headache, sedation (sedation has been reported more frequently in children and adolescents than in adults. Sedation is usually mild and transient).

Uncommon: drowsiness, fatigue, dizziness, concentration difficulties, extrapyramidal symptoms: involuntary shaking (tremor), muscular stiffness (rigidity), increased salivation, slowness of movements (bradykinesia), restless legs (akathisia), sudden muscular contractions (acute dystonia) (these symptoms are usually mild and are reversible upon dose reduction and/or administration of antiparkinson drugs, if necessary)

Very rare: movement disorders (tardive dyskinesia), neuroleptic malignant syndrome with symptoms such as fever, muscular stiffness, lowering of the level of consciousness, fits (seizures), panic reactions

Eye disorders

Uncommon: blurred vision

Heart

Uncommon: increased heart rate (tachycardia)

Very rare: specific cardiac arrhythmias (QT prolongation, torsades de pointes)

Blood vessels

Uncommon: low blood pressure (hypotension) including dizziness on getting up (orthostatic hypotension) or high blood pressure (hypertension)

Rare: strokes or temporary reduction of blood flow to the brain (TIA's)

Respiration and chest

Uncommon: cold (rhinitis)

Stomach and intestine

Uncommon: constipation, digestive disorders (dyspepsia), nausea/vomiting, stomach ache, weight increase

Liver

Very rare: rise in liver values (hepatic enzymes)

Skin and subcutaneous tissue

Uncommon: rash and other allergic reactions Very rare: swelling, itching and inflamed skin (pruritus, exanthema), photosensitivity

Kidney and urinary tract

Uncommon: urinary incontinence

Sex organs and breasts

Uncommon: erectile dysfunction, dysfunctional ejaculation and orgasm disturbances, impotence in men who previously did not have any sexual disturbances Rare: prolonged painful erection (priapism)

Muscles

Very rare: muscle weakness

Others

Very rare: abnormally lowered body temperature (hypothermia), abnormally elevated body temperature (hyperthermia)

In rare cases, Risperidone may cause a disturbance of the water balance due to overdrinking or disturbances in the secretion of a specific hormone (antidiuretic hormone).

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

5.    How to store Risperidone

Keep out of the reach and sight of children.

Do not use after the exiry date stated on the package.

This medicinal product does not require any special storage conditions.

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 to protect the environment.

6.    Further information

What Risperidone contains

■    The active ingredient is risperidone. Each tablet contains 1 mg risperidone.

■    Other ingredients are mannitol (E421), basic butylated methacrylate copolymer, povidone K-25, microcrystalline cellulose, hydroxypropylcellulose, aspartame (E951), crospovidone, red iron oxide (E172), spearmint flavour, peppermint flavour, calcium silicate, magnesium stearate.

What Risperidone looks like and contents of the pack

Orodispersible Tablets:

Tablets are round, slightly convex, pink marbled tablets. Contents of the packs: 28 or 56 in blister pack.

Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Marketing Authorisation Holder:

KRKA, d.d., Novo mesto, Smarjeska cesta 6,

8501 Novo mesto, Slovenia Manufacturer:

KRKA, d.d., Novo mesto, Smarjeska cesta 6,

8501 Novo mesto, Slovenia

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

Czech Rep Rorendo Q-Tab 1 mg, orodispersible tablets Germany Risperidon Krka 1 mg Schmelztabletten Denmark    Risperidon Krka

Estonia    Torendo Q-Tab 1 mg

Finland Risperidon Norpharm 1 mg Orodispersible Tablets

Hungary Torendo Q-Tab 1 mg Lithuania Torendo Q-Tab 1 mg, orodispersible tablets Latvia    Torendo Q-Tab 1 mg

Norway    Risperidon Krka 1 mg    Orodispersible Tablets

Poland    Torendo Q-Tab 1 mg

Portugal    Risperidon Krka

Sweden    Risperidon Krka 1 mg    ODT tablet

Slovak Rep Torendo Q-Tab 1 mg

This leaflet was last approved: 27/09/2006