Mayzent

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
16-01-2024
Toote omadused Toote omadused (SPC)
16-01-2024
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
23-01-2020

Toimeaine:

Siponimod fumaric acid

Saadav alates:

Novartis Europharm Limited 

ATC kood:

L04

INN (Rahvusvaheline Nimetus):

siponimod

Terapeutiline rühm:

Selective immunosuppressants

Terapeutiline ala:

Multiple Sclerosis, Relapsing-Remitting

Näidustused:

Mayzent is indicated for the treatment of adult patients with secondary progressive multiple sclerosis (SPMS) with active disease evidenced by relapses or imaging features of inflammatory activity.

Toote kokkuvõte:

Revision: 10

Volitamisolek:

Authorised

Loa andmise kuupäev:

2020-01-13

Infovoldik

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of
new safety information. Healthcare professionals are asked to report
any suspected adverse reactions.
See section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
Mayzent 0.25 mg film-coated tablets
Mayzent 1 mg film-coated tablets
Mayzent 2 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Mayzent 0.25 mg film-coated tablets
Each film-coated tablet contains siponimod fumaric acid equivalent to
0.25 mg siponimod.
_Excipient with known effect _
Each tablet contains 59.1 mg lactose (as monohydrate) and 0.092 mg
soya lecithin.
Mayzent 1 mg film-coated tablets
Each film-coated tablet contains siponimod fumaric acid equivalent to
1 mg siponimod.
_Excipient with known effect _
Each tablet contains 58.3 mg lactose (as monohydrate) and 0.092 mg
soya lecithin.
Mayzent 2 mg film-coated tablets
Each film-coated tablet contains siponimod fumaric acid equivalent to
2 mg siponimod.
_Excipient with known effect _
Each tablet contains 57.3 mg lactose (as monohydrate) and 0.092 mg
soya lecithin.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet
Mayzent 0.25 mg film-coated tablets
Pale red, round, biconvex, bevelled-edged film-coated tablet of
approximately 6.1 mm diameter with
company logo on one side and “T” on the other side.
Mayzent 1 mg film-coated tablets
Violet white, round, biconvex, bevelled-edged film-coated tablet of
approximately 6.1 mm diameter
with company logo on one side and “L” on the other side.
Mayzent 2 mg film-coated tablets
Pale yellow, round, biconvex, bevelled-edged film-coated tablet of
approximately 6.1 mm diameter
with company logo on one side and “II” on the other side.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Mayzent is indicated for the treatment of adult patients with
secondary progressive multiple sclerosis
(SPMS) with active disease evidenced by r
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of
new safety information. Healthcare professionals are asked to report
any suspected adverse reactions.
See section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
Mayzent 0.25 mg film-coated tablets
Mayzent 1 mg film-coated tablets
Mayzent 2 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Mayzent 0.25 mg film-coated tablets
Each film-coated tablet contains siponimod fumaric acid equivalent to
0.25 mg siponimod.
_Excipient with known effect _
Each tablet contains 59.1 mg lactose (as monohydrate) and 0.092 mg
soya lecithin.
Mayzent 1 mg film-coated tablets
Each film-coated tablet contains siponimod fumaric acid equivalent to
1 mg siponimod.
_Excipient with known effect _
Each tablet contains 58.3 mg lactose (as monohydrate) and 0.092 mg
soya lecithin.
Mayzent 2 mg film-coated tablets
Each film-coated tablet contains siponimod fumaric acid equivalent to
2 mg siponimod.
_Excipient with known effect _
Each tablet contains 57.3 mg lactose (as monohydrate) and 0.092 mg
soya lecithin.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet
Mayzent 0.25 mg film-coated tablets
Pale red, round, biconvex, bevelled-edged film-coated tablet of
approximately 6.1 mm diameter with
company logo on one side and “T” on the other side.
Mayzent 1 mg film-coated tablets
Violet white, round, biconvex, bevelled-edged film-coated tablet of
approximately 6.1 mm diameter
with company logo on one side and “L” on the other side.
Mayzent 2 mg film-coated tablets
Pale yellow, round, biconvex, bevelled-edged film-coated tablet of
approximately 6.1 mm diameter
with company logo on one side and “II” on the other side.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Mayzent is indicated for the treatment of adult patients with
secondary progressive multiple sclerosis
(SPMS) with active disease evidenced by r
                                
                                Lugege kogu dokumenti
                                
                            

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