SIGNIFOR LAR 20 MG

국가: 이스라엘

언어: 영어

출처: Ministry of Health

지금 구매하세요

환자 정보 전단 환자 정보 전단 (PIL)
23-11-2023
제품 특성 요약 제품 특성 요약 (SPC)
02-11-2023
공공 평가 보고서 공공 평가 보고서 (PAR)
05-08-2020

유효 성분:

PASIREOTIDE AS EMBONATE

제공처:

MEDISON PHARMA LTD

ATC 코드:

H01CB05

약제 형태:

POWDER AND SOLVENT FOR SUSPENSION FOR INJECTION

구성:

PASIREOTIDE AS EMBONATE 20 MG/VIAL

관리 경로:

I.M

처방전 유형:

Required

Manufactured by:

RECORDATI RARE DISEASES, FRANCE

치료 영역:

PASIREOTIDE

치료 징후:

Signifor LAR is indicated for the treatment of adult patients with acromegaly for whom surgery is not an option or has not been curative and who are inadequately controlled on treatment with another somatostatin analogue.Treatment of adult patients with Cushing’s disease for whom surgery is not an option or for whom surgery has failed.

승인 날짜:

2020-10-31

환자 정보 전단

                                Signifor LAR 10 mg-20 mg-30 mg-40 mg-60 mg-PIL-1023-V1
Signifor LAR-10mg_20mg_30mg_40mg_60mg-PIL-ENG-D17-F
Page 1 of 12
PATIENT LEAFLET IN ACCORDANCE WITH THE PHARMACISTS' REGULATIONS
(PREPARATIONS) - 1986
The medicine is dispensed with a doctor’s
prescription only
SIGNIFOR
® LAR
1
0 MG, POWDER AND SOLVENT FOR SUSPENSION FOR
INJECTION
The active ingredient and its quantity:
Each vial of powder contains: 10 mg pasireotide (as pamoate)
SIGNIFOR
® LAR 20 MG, POWDER AND SOLVENT FOR SUSPENSION FOR
INJECTION
The active ingredient and its quantity:
Each vial of powder contains: 20 mg pasireotide (as pamoate)
SIGNIFOR
® LAR 30 MG, POWDER AND SOLVENT FOR SUSPENSION FOR
INJECTION
The active ingredient and its quantity:
Each vial of powder contains: 30 mg pasireotide (as pamoate)
SIGNIFOR
® LAR 40 MG, POWDER AND SOLVENT FOR SUSPENSION FOR
INJECTION
The active ingredient and its quantity:
Each vial of powder contains: 40 mg pasireotide (as pamoate)
SIGNIFOR
® LAR 60 MG, POWDER AND SOLVENT FOR SUSPENSION FOR
INJECTION
The active ingredient and its quantity:
Each vial of powder contains: 60 mg pasireotide (as pamoate)
INACTIVE AND ALLERGENIC INGREDIENTS:
see section 6 'Additional information' and section 2
'Important information about some of this medicine's ingredients'.
READ THE ENTIRE LEAFLET CAREFULLY BEFORE YOU START USING THIS
MEDICINE.
This leaflet
contains concise information about this medicine. If you have further
questions, refer to the
doctor or pharmacist.
This medicine has been prescribed to treat your illness. Do not pass
it on to others. It may
harm them, even if it seems to you that their illness is similar to
yours.
1. WHAT IS THIS MEDICINE INTENDED FOR?
Signifor LAR is indicated for the treatment of adult patients with
acromegaly for whom
surgery is not an option or has not been curative and who are
inadequately controlled on
treatment with other somatostatin analogues.
It is also indicated for treatment of Cushing’s disease in adult
patients
for whom surgical
treatment is not an option or for whom 
                                
                                전체 문서 읽기
                                
                            

제품 특성 요약

                                Signifor LAR 10 mg-20 mg-30 mg-40 mg-60 mg-SPC-1023-V1
Page 1 of 19
1.
NAME OF THE MEDICINAL PRODUCT
Signifor LAR 10 mg
Signifor LAR 20 mg
Signifor LAR 30 mg
Signifor LAR 40 mg
Signifor LAR 60 mg
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
One vial contains:
Signifor LAR 10 mg: 10 mg pasireotide (as pasireotide pamoate).
Signifor LAR 20 mg: 20 mg pasireotide (as pasireotide pamoate).
Signifor LAR 30 mg: 30 mg pasireotide (as pasireotide pamoate).
Signifor LAR 40 mg: 40 mg pasireotide (as pasireotide pamoate).
Signifor LAR 60 mg: 60 mg pasireotide (as pasireotide pamoate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder and solvent for suspension for injection.
Powder: slightly yellowish to yellowish powder.
Solvent: clear, colourless to slightly yellow or slightly brown
solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Signifor LAR is indicated for the treatment of adult patients with
acromegaly for whom surgery is not
an option or has not been curative and who are inadequately controlled
on treatment with another
somatostatin analogue.
Treatment of adult patients with Cushing’s disease for whom surgery
is not an option or for whom
surgery has failed.
The 60 mg strength is only to be used in the treatment of acromegaly.
The 10 mg and 30 mg are
only to be used in the treatment of Cushing’s disease.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Acromegaly _
The recommended initial dose for the treatment of acromegaly
is 40 mg of pasireotide every 4 weeks.
The dose may be increased to a maximum of 60 mg for patients whose
growth hormone (GH) and/or
insulin-like growth factor-1 (IGF-1) levels are not fully controlled
after 3 months of treatment with
Signifor LAR at 40 mg.
Signifor LAR 10 mg-20 mg-30 mg-40 mg-60 mg-SPC-1023-V1
Page 2 of 19
Management of suspected adverse reactions or over-response to
treatment (IGF-1 < lower limit of
normal) may require temporary dose reduction of Signifor LAR. The dose
may be decreased either
temporarily or permanently.
_Cushing
                                
                                전체 문서 읽기
                                
                            

다른 언어로 된 문서

환자 정보 전단 환자 정보 전단 아랍어 23-11-2023
환자 정보 전단 환자 정보 전단 히브리어 02-11-2023

이 제품과 관련된 검색 알림