Lenalidomide ratiopharm 7,5 mg, harde capsules

Šalis: Nyderlandai

kalba: olandų

Šaltinis: CBG-MEB (College ter Beoordeling van Geneesmiddelen)

Nusipirk tai dabar

Parsisiųsti Pakuotės lapelis (PIL)
13-07-2023
Parsisiųsti Prekės savybės (SPC)
13-07-2023

Veiklioji medžiaga:

LENALIDOMIDEHYDROCHLORIDE 1-WATER 9,1 mg/stuk SAMENSTELLING overeenkomend met ; LENALIDOMIDE 7,5 mg/stuk

Prieinama:

Ratiopharm GmbH Graf-Arco-Strasse 3 89079 ULM (DUITSLAND)

ATC kodas:

L04AX04

INN (Tarptautinis Pavadinimas):

LENALIDOMIDEHYDROCHLORIDE 1-WATER 9,1 mg/stuk SAMENSTELLING overeenkomend met ; LENALIDOMIDE 7,5 mg/stuk

Vaisto forma:

Capsule, hard

Sudėtis:

AMMONIA (E 527) ; CELLULOSE, MICROKRISTALLIJN (E 460(i)) ; CROSCARMELLOSE NATRIUM (E 468) ; GELATINE (E 441) ; IJZEROXIDE GEEL (E 172) ; IJZEROXIDE ZWART (E 172) ; KALIUMHYDROXIDE (E 525) ; PROPYLEENGLYCOL (E 1520) ; SCHELLAK (E 904) ; SILICIUMDIOXIDE (E 551) ; TALK (E 553 B) ; TITAANDIOXIDE (E 171) ; ZWARTE INKT, AMMONIA (E 527) ; CELLULOSE, MICROKRISTALLIJN (E 460) ; CROSCARMELLOSE NATRIUM (E 468) ; GELATINE (E 441) ; IJZEROXIDE GEEL (E 172) ; IJZEROXIDE ZWART (E 172) ; KALIUMHYDROXIDE (E 525) ; PROPYLEENGLYCOL (E 1520) ; SCHELLAK (E 904) ; SILICIUMDIOXIDE (E 551) ; TALK (E 553 B) ; TITAANDIOXIDE (E 171) ; ZWARTE INKT

Vartojimo būdas:

Oraal gebruik

Gydymo sritis:

Lenalidomide

Leidimo data:

2018-11-20

Pakuotės lapelis

                                Lenalidomide, NL/H/4068/001-007, 08.03.2023
1
rvg 121419_33_34_36_38_41_46 EU PIL IB/024/G met NL info-tracked
BIJSLUITER: INFORMATIE VOOR DE GEBRUIKER
LENALIDOMIDE RATIOPHARM 2,5 MG, HARDE CAPSULES
LENALIDOMIDE RATIOPHARM 5 MG, HARDE CAPSULES
LENALIDOMIDE RATIOPHARM 7,5 MG, HARDE CAPSULES
LENALIDOMIDE RATIOPHARM 10 MG, HARDE CAPSULES
LENALIDOMIDE RATIOPHARM 15 MG, HARDE CAPSULES
LENALIDOMIDE RATIOPHARM 20 MG, HARDE CAPSULES
LENALIDOMIDE RATIOPHARM 25 MG, HARDE CAPSULES
lenalidomide
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
-
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 only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What [Product name] is and what it is used for
2.
What you need to know before you take [Product name]
3.
How to take [Product name]
4.
Possible side effects
5.
How to store [Product name]
6.
Contents of the pack and other information
1.
WHAT [PRODUCT NAME] IS AND WHAT IT IS USED FOR
WHAT [PRODUCT NAME] IS
[Product name] contains the active substance ‘lenalidomide’. This
medicine belongs to a group of
medicines which affect how your immune system works.
WHAT {PRODUCT NAME] IS USED FOR
[Product name] is used in adults for
•
Multiple myeloma
•
Myelodysplastic syndromes
•
Mantle cell lymphoma
•
Follicular lymphoma
MULTIPLE MY
ELOMA
Multiple myeloma is a type of cancer which affects a certain kind of
white blood cell, called the plasma
cell. These cells collect in the bone marrow and divide, becoming out
of control. This can damage the
bones and kidneys.
Multiple myeloma generally cannot be cured. However, the signs and
symptoms can be greatly reduced
or disappear fo
                                
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Prekės savybės

                                Lenalidomide, NL/H/4068/001-007, 08.03.2023
1
rvg 121419_33_34_36_38_41_46 EU SPC IB/024/G met NL info-tracked
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAAM VAN HET GENEESMIDDEL
Lenalidomide ratiopharm 2,5 mg, harde capsules
Lenalidomide ratiopharm 5 mg, harde capsules
Lenalidomide ratiopharm 7,5 mg, harde capsules
Lenalidomide ratiopharm 10 mg, harde capsules
Lenalidomide ratiopharm 15 mg, harde capsules
Lenalidomide ratiopharm 20 mg, harde capsules
Lenalidomide ratiopharm 25 mg, harde capsules
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
[Product name] 2.5 mg hard capsules
Each capsule contains lenalidomide hydrochloride hydrate corresponding
to 2.5 mg of lenalidomide.
[Product name] 5 mg hard capsules
Each capsule contains lenalidomide hydrochloride hydrate corresponding
to 5 mg of lenalidomide.
[Product name] 7.5 mg hard capsules
Each capsule contains lenalidomide hydrochloride hydrate corresponding
to 7.5 mg of lenalidomide.
[Product name] 10 mg hard capsules
Each capsule contains lenalidomide hydrochloride hydrate corresponding
to 10 mg of lenalidomide.
[Product name] 15 mg hard capsules
Each capsule contains lenalidomide hydrochloride hydrate corresponding
to 15 mg of lenalidomide.
[Product name] 20 mg hard capsules
Each capsule contains lenalidomide hydrochloride hydrate corresponding
to 20 mg of lenalidomide.
[Product name] 25 mg hard capsules
Each capsule contains lenalidomide hydrochloride hydrate corresponding
to 25 mg of lenalidomide.
Excipients with known effect:
[Product name] 2.5 mg hard capsules:
Each capsule contains 0.5 mg of sodium.
[Product name] 5 mg hard capsules:
Each capsule contains 0.5 mg of sodium.
[Product name] 7.5 mg hard capsules:
Each capsule contains 0.67 mg of sodium.
[Product name] 10 mg hard capsules:
Each capsule contains 0.9 mg of sodium.
[Product name] 15 mg hard capsules:
Each capsule contains 1.35 mg of sodium.
[Product name] 20 mg hard capsules:
Each capsule contains 1.80 mg of sodium.
Lenalidomide, NL/H/4068/001-007, 08.03.2023
2
rvg 121419_33_34_36_38_41_46 EU SPC IB/024/G
                                
                                Perskaitykite visą dokumentą