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Rispercol

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Package leaflet: information for the patient


Rispercol 0.5 mg orodispersible tablets

Rispercol 1 mg orodispersible tablets

Rispercol 2 mg orodispersible tablets

Risperidone


Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.


What is in this leaflet

1. What Rispercolis and what it is used for

2. What you need to know before you take Rispercol

3. How to take Rispercol

4. Possible side effects

5. How to store Rispercol

6. Contents of the pack and other information


1. What Rispercol is and what it is used for


Rispercol belongs to a group of medicines called ‘anti-psychotics’.


Rispercol is used to treat the following:



2. What you need to know before you take Rispercol


Do not take Rispercol

if you are allergic to risperidone or any of the other ingredients of this medicine (listed in section 6).


If you are not sure if the above applies to you, talk to your doctor or pharmacist before using Rispercol.


Warnings and precautions

Talk to your doctor or pharmacist before taking Rispercol.


If you are not sure if any of the above applies to you, talk to your doctor or pharmacist before using Rispercol.


As dangerously low numbers of a certain type of white blood cell needed to fight infection in your blood has been seen very rarely with patients taking risperidone, your doctor may check your white blood cell counts.


Rispercol may cause you to gain weight. Significant weight gain may adversely affect your health. Your doctor should regularly measure your body weight.


As diabetes mellitus or worsening of pre-existing diabetes mellitus have been seen with patients taking Rispercol, your doctor should check for signs of high blood sugar. In patients with pre-existing diabetes mellitus blood glucose should be monitored regularly.


During an operation on the eye for cloudiness of the lens (cataract), the pupil (the black circle in the middle of your eye) may not increase in size as needed. Also, the iris (the coloured part of the eye) may become floppy during surgery and that may lead to eye damage. If you are planning to have an operation on your eye, make sure you tell your eye doctor that you are taking this medicine.


Elderly people with dementia

In elderly patients with dementia, there is an increased risk of stroke. You should not take risperidone if you have dementia caused by stroke.

During treatment with risperidone you should frequently see your doctor.

Medical treatment should be sought straight away if you or your care‑giver notice a sudden change in your mental state or sudden weakness or numbness of your face, arms or legs, especially on one side, or slurred speech, even for a short period of time. These may be signs of a stroke.


Children and adolescents

Before treatment is started in conduct disorder, other causes of aggressive behaviour should have been ruled out.

If during treatment with risperidone tiredness occurs, a change in the time of administration might improve attention difficulties.

Before treatment is started you, or your child’s body weight may be measured and it may be regularly monitored during treatment.


Other medicines and Rispercol

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


It is especially important to talk to your doctor or pharmacist if you are taking any of the following:


The following medicines may reduce the effect of risperidone

If you start or stop taking such medicines you may need a different dose of risperidone.


The following medicines may increase the effect of risperidone

If you start or stop taking such medicines you may need a different dose of risperidone.


If you are not sure if any of the above applies to you, talk to your doctor or pharmacist before using Rispercol.


Rispercol with food, drink and alcohol

You can take this medicine with or without food. You should avoid drinking alcohol when taking Rispercol.


Pregnancy and breast-feedingand fertility


Driving and using machines

Dizziness, tiredness, and vision problems may occur during treatment with Rispercol. Do not drive or use any tools or machines without talking to your doctor first.


Rispercol containsaspartame and sorbitol

Aspartame (E951) contains a source of phenylalanine. May be harmful for people with phenylketonuria.

Rispercol orodispersible tablets contain sorbitol also. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.


3. How to take Rispercol

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.


How much to take


For the treatment of schizophrenia


Adults


Elderly people


Children and adolescents

Children and adolescents under 18 years old should not be treated with Rispercol for schizophrenia.


For the treatment of mania


Adults


Elderly people


Children and adolescents

Children and adolescents under 18 years old should not be treated with Rispercol for bipolar mania.


For the treatment of long-standing aggression in people with Alzheimer’s dementia


Adults (including elderly people)


For the treatment of conduct disorder in children and adolescents


The dose will depend on your child’s weight:


For children who weigh less than 50 kg


For children who weigh 50 kg or more

The starting dose will normally be 0.5 mg once a day


Treatment duration in patients with conduct disorder should be not more than 6 weeks.


Children under 5 years old should not be treated with Rispercol for conduct disorder.


People with kidney or liver problems

Regardless of the disease to be treated, all starting doses and following doses of risperidone should be halved. Dose increases should be slower in these patients.


Risperidone should be used with caution in this patient group.


How to take Rispercol

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.


Your doctor will tell you how much medicine to take and for how long. This will depend on your condition and varies from person to person. The amount of medicine you should take is explained under the ‘How much to take’ sub-heading below.


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

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

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

Tip the tablet out onto your hand.

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.


If you take more Rispercol than you should


If you forget to take Rispercol


If you stop taking Rispercol

You should not stop taking this medicine unless told to do so by your doctor. Your symptoms may return. If your doctor decides to stop this medicine, your dose may be decreased gradually over a few days.


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, although not everybody gets them.


Tell your doctor immediately if you:


The following side effects may happen:

Very Common (affects more than 1 user in 10):


Common (affects 1 to 10 users in 100):


Uncommon (affects 1 to 10 users in 1000):


Rare (affects 1 to 10 users in 10,000):


Very rare (affects less than 1 user in 10,000):


The following side effect has been seen with the use of another medicine called paliperidone that is very similar to risperidone, so these can also be expected withRispercol: Rapid heartbeat upon standing.


Additional side effects in children and adolescents

In general, side effects in children are expected to be similar to those in adults.

The following side effects were reported more often in children and adolescents (5 to 17 years) than in adults: feeling sleepy, or less alert, fatigue (tiredness), headache, increased appetite, vomiting, common cold symptoms, nasal congestion, abdominal pain, dizziness, cough, fever, tremor (shaking), diarrhoea, and incontinence (lack of control) of urine.


Reportingof 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 reporting system listed in Appendix V. By reporting side effects you can help provide more information on the safety of this medicine.


5. How to store Rispercol


Keep this medicine out of the sight and reach of children.


Do not use after the expiry date which is stated on the blister and outer carton after EXP. The expiry date refers to the last day of that month.


This medicine does not require any special storage conditions.


Donot throw away any medicinesvia wastewater or household waste. Ask your pharmacist how to throw awaymedicines you no longer use. These measures will help protect the environment.


6. Contents of the pack and other information


What Rispercol contains

The active substance is risperidone.

Each orodispersible tablet contains 0.5 mg, 1mgor 2mgrisperidone.

The other ingredients are mannitol, basic butylated methacrylate copolymer, povidone K25, microcrystalline cellulose, low-substituted hydroxypropylcellulose, aspartame (E951), crospovidone, red iron oxide (E172), spearmint flavour, peppermint flavour (containing in particular sorbitol (E420), levomenthol), calcium silicate, magnesium stearate.


What Rispercol looks like and contents of the pack

Round, slightly convex, pink marbled orodispersible tablets.


Pack sizes of 10, 20, 28, 30, 56 and 60orodispersible tablets.

Not all pack sizes may be marketed.


Marketing Authorisation Holder and Manufacturer


<To be completed nationally.>


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


<To be completed nationally.>


This leaflet was last revised in 2014-09-24