Lenalidomide Krka d.d.

Nchi: Umoja wa Ulaya

Lugha: Kiingereza

Chanzo: EMA (European Medicines Agency)

Nunua Sasa

Taarifa za kipeperushi Taarifa za kipeperushi (PIL)
10-07-2023
Tabia za bidhaa Tabia za bidhaa (SPC)
10-07-2023

Viambatanisho vya kazi:

lenalidomide hydrochloride hydrate

Inapatikana kutoka:

Krka, d.d., Novo mesto 

ATC kanuni:

L04AX04

INN (Jina la Kimataifa):

lenalidomide

Kundi la matibabu:

Immunosuppressants

Eneo la matibabu:

Multiple Myeloma; Lymphoma, Follicular; Myelodysplastic Syndromes

Matibabu dalili:

Multiple myelomaLenalidomide Krka d.d. as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation.Lenalidomide Krka d.d. as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4.2) is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant.Lenalidomide Krka d.d. in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy.Myelodysplastic syndromesLenalidomide Krka d.d. as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate.Follicular lymphomaLenalidomide Krka d.d. in combination with rituximab (anti-CD20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (Grade 1 – 3a).

Bidhaa muhtasari:

Revision: 2

Idhini hali ya:

Withdrawn

Idhini ya tarehe:

2021-02-11

Taarifa za kipeperushi

                                84
B. PACKAGE LEAFLET
Medicinal product no longer authorised
85
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
LENALIDOMIDE KRKA D.D. 2.5 MG HARD CAPSULES
LENALIDOMIDE KRKA D.D. 5 MG HARD CAPSULES
LENALIDOMIDE KRKA D.D. 7.5 MG HARD CAPSULES
LENALIDOMIDE KRKA D.D. 10 MG HARD CAPSULES
LENALIDOMIDE KRKA D.D. 15 MG HARD CAPSULES
LENALIDOMIDE KRKA D.D. 20 MG HARD CAPSULES
LENALIDOMIDE KRKA D.D. 25 MG HARD 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 Lenalidomide Krka d.d. is and what it is used for
2.
What you need to know before you take Lenalidomide Krka d.d.
3.
How to take Lenalidomide Krka d.d.
4.
Possible side effects
5.
How to store Lenalidomide Krka d.d.
6.
Contents of the pack and other information
1.
WHAT LENALIDOMIDE KRKA D.D. IS AND WHAT IT IS USED FOR
WHAT LENALIDOMIDE KRKA D.D. IS
Lenalidomide Krka d.d. contains the active substance
‘lenalidomide’. This medicine belongs to a
group of medicines which affect how your immune system works.
WHAT LENALIDOMIDE KRKA D.D. IS USED FOR
Lenalidomide Krka d.d. is used in adults for:
-
Multiple myeloma
-
Myelodysplastic syndromes
-
Follicular lymphoma
MULTIPLE MYELOMA
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 for a period of time. Thi
                                
                                Soma hati kamili
                                
                            

Tabia za bidhaa

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Lenalidomide Krka d.d. 2.5 mg hard capsules
Lenalidomide Krka d.d. 5 mg hard capsules
Lenalidomide Krka d.d. 7.5 mg hard capsules
Lenalidomide Krka d.d. 10 mg hard capsules
Lenalidomide Krka d.d. 15 mg hard capsules
Lenalidomide Krka d.d. 20 mg hard capsules
Lenalidomide Krka d.d. 25 mg hard capsules
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each hard capsule contains lenalidomide hydrochloride monohydrate
equivalent to 2.5 mg, 5 mg,
7.5 mg, 10 mg, 15 mg, 20 mg or 25 mg lenalidomide.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Hard capsule (capsule)
Lenalidomide Krka d.d. 2.5 mg hard capsules
Capsule cap is green, capsule body is green with imprinted black mark
2.5. Capsule content is white to
yellow white or to brown white powder. Hard capsule size: 4, length 14
± 1 mm.
Lenalidomide Krka d.d. 5 mg hard capsules
Capsule cap is blue, capsule body is blue with imprinted black mark 5.
Capsule content is white to
yellow white or to brown white powder. Hard capsule size: 2, length 18
± 1 mm.
Lenalidomide Krka d.d. 7.5 mg hard capsules
Capsule cap is brown, capsule body is brown with imprinted white mark
7.5. Capsule content is white
to yellow white or to brown white powder. Hard capsule size: 1, length
19 ± 1 mm.
Lenalidomide Krka d.d. 10 mg hard capsules
Capsule cap is green, capsule body is brown with imprinted white mark
10. Capsule content is white to
yellow white or to brown white powder. Hard capsule size: 0, length 21
± 1 mm.
Lenalidomide Krka d.d. 15 mg hard capsules
Capsule cap is brown, capsule body is blue with imprinted black mark
15. Capsule content is white to
yellow white or to brown white powder. Hard capsule size: 2, length 18
± 1 mm.
Lenalidomide Krka d.d. 20 mg hard capsules
Capsule cap is green, capsule body is blue with imprinted black mark
20. Capsule content is white to
yellow white or to brown white powder. Hard capsule size: 1, length 19
± 
                                
                                Soma hati kamili
                                
                            

Nyaraka katika lugha zingine

Taarifa za kipeperushi Taarifa za kipeperushi Kibulgaria 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kibulgaria 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kibulgaria 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kihispania 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kihispania 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihispania 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kicheki 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kicheki 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kicheki 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kidenmaki 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kidenmaki 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kidenmaki 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kijerumani 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kijerumani 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kijerumani 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiestonia 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kiestonia 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiestonia 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kigiriki 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kigiriki 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kigiriki 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kifaransa 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kifaransa 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifaransa 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiitaliano 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kiitaliano 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiitaliano 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kilatvia 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kilatvia 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilatvia 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kilithuania 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kilithuania 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilithuania 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kihungari 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kihungari 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihungari 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kimalta 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kimalta 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kimalta 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiholanzi 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kiholanzi 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiholanzi 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kipolandi 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kipolandi 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kipolandi 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kireno 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kireno 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kireno 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiromania 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kiromania 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiromania 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kislovakia 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kislovakia 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovakia 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kislovenia 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kislovenia 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovenia 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kifinlandi 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kifinlandi 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifinlandi 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiswidi 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kiswidi 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiswidi 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kinorwe 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kinorwe 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kiaisilandi 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kiaisilandi 10-07-2023
Taarifa za kipeperushi Taarifa za kipeperushi Kroeshia 10-07-2023
Tabia za bidhaa Tabia za bidhaa Kroeshia 10-07-2023
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kroeshia 10-07-2023

Tafuta arifu zinazohusiana na bidhaa hii