COMTAN TABLET 200MG

Država: Malezija

Jezik: engleski

Izvor: NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

Kupi sada

Svojstava lijeka Svojstava lijeka (SPC)
20-09-2020

Aktivni sastojci:

ENTACAPONE

Dostupno od:

ORION PHARMA (MY) SDN. BHD.

INN (International ime):

ENTACAPONE

Jedinice u paketu:

100 Tablets; 30 Tablets

Proizveden od:

ORION CORP

Svojstava lijeka

                                156657-1
COMTAN®
Catechol-O-methyl transferase inhibitor
COMPOSITION AND PHARMACEUTICAL FORM
Tablet containing 200 mg entacapone.
For a full list of excipients, see section EXCIPIENTS.
Brownish-orange, oval, biconvex film-coated tablet with
Comtan® engraved on one side.
INDICATIONS
Entacapone is indicated as an adjunct to standard
preparations of levodopa/benserazide or levodopa/
carbidopa for use in patients with Parkinson’s disease and
end-of-dose motor fluctuations, who cannot be stabilized
on those combinations.
DOSAGE AND ADMINISTRATION
Entacapone should only be used in combination with
levodopa/benserazide or levodopa/carbidopa. The
prescribing information for these levodopa preparations
is applicable to their concomitant use with entacapone.
POSOLOGY
One 200 mg tablet is taken with each levodopa/
dopa decarboxylase inhibitor dose. The maximum
recommended dose is 200 mg ten times daily, i.e.
2,000 mg of entacapone.
Entacapone enhances the effects of levodopa. Hence, to
reduce levodopa-related dopaminergic adverse reactions,
e.g. dyskinesias, nausea, vomiting and hallucinations, it is
often necessary to adjust levodopa dosage within the first
days to first weeks after initiating entacapone treatment.
The daily dose of levodopa should be reduced by about
10 to 30% by extending the dosing intervals and/or by
reducing the amount of levodopa per dose, according to
the clinical condition of the patient.
Entacapone increases the bioavailability of levodopa from
standard levodopa/benserazide preparations slightly
more (5 to 10%) than from standard levodopa/carbidopa
preparations. Hence, patients who are taking standard
levodopa/benserazide preparations may need a larger
reduction of their levodopa dose when entacapone is
initiated.
If entacapone treatment is discontinued, it is necessary to
adjust the dosing of other antiparkinsonian treatments,
especially levodopa, to achieve a sufficient level of control
of the parkinsonian symptoms.
Renal impairment does not affect the pharmacokinetics
of entacapone and ther
                                
                                Pročitajte cijeli dokument
                                
                            

Dokumenti na drugim jezicima

Uputa o lijeku Uputa o lijeku malajski 31-03-2021

Upozorenja za pretraživanje vezana za ovaj proizvod

Pogledajte povijest dokumenata