Voorbeelden van het gebruik van Corbilta in het Engels en hun vertalingen in het Nederlands
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How to store Corbilta.
Why is Corbilta approved?
Other information about Corbilta.
How is Corbilta used?
Corbilta contains sucrose 1.2 mg/tablet.
You should not breast-feed during treatment with Corbilta.
Corbilta may be taken with or without food.
Women should not breast-feed during treatment with Corbilta.
Corbilta must not be used in patients with.
If you must undergo surgery, please tell your doctor that you are using Corbilta.
Corbilta may induce orthostatic hypotension.
The possibility that the patient has taken other active substances in addition to Corbilta should be taken into consideration.
Corbilta may make it harder for you to digest iron.
Paediatric population: The safety and efficacy of Corbilta in children aged below 18 years have not been established.
What Corbilta looks like and contents of the pack?
If other levodopa products are used concomitantly with a Corbilta tablet, the maximum dose recommendations should be followed.
Corbilta is used for the treatment of Parkinson's disease.
neuroleptic malignant syndrome may occur with Corbilta although no cases have been identified from the clinical trial data.
Corbilta comes in six different pack sizes 10,
a general medical evaluation including liver function should be considered feel the need to stop using Corbilta, see section'If you stop taking Corbilta. .
Corbilta is a medicine that contains three active substances:
Patients who are currently treated with entacapone and with standard release levodopa/carbidopa in doses equal to Corbilta tablet strengths can be directly transferred to corresponding Corbilta tablets.
Corbilta is not recommended for the treatment of drug-induced extrapyramidal reactions.
At the initiation, Corbilta should be adjusted to correspond as closely as possible to the total daily dose of levodopa currently used.
Corbilta contains three active substances(levodopa,
Corbilta is used when these fluctuations cannot be treated with the standard combination alone.
Each Corbilta 100 mg/25 mg/200 mg tablet contains 100 mg of levodopa, 25 mg of carbidopa and 200 mg of entacapone.
Corbilta should not be used during pregnancy unless the benefits for the mother outweigh the possible risks to the foetus.
Usually Corbilta is to be used in patients who are currently treated with corresponding doses of standard release levodopa/DDC inhibitor and entacapone.
Corbilta is not recommended to be used for treatment of extrapyramidal symptoms(e.g. involuntary movements,