METOCLOPRAMIDE S.A.L.F 10 MG2 ML

국가: 이스라엘

언어: 영어

출처: Ministry of Health

지금 구매하세요

Download 제품 특성 요약 (SPC)
25-12-2023
Download 공공 평가 보고서 (PAR)
04-08-2022

유효 성분:

METOCLOPRAMIDE HYDROCHLORIDE

제공처:

RAZ PHARMACEUTICS LTD, ISRAEL

ATC 코드:

A03FA01

약제 형태:

SOLUTION FOR INJECTION

구성:

METOCLOPRAMIDE HYDROCHLORIDE 5 MG/ML

관리 경로:

I.M, I.V

처방전 유형:

Required

Manufactured by:

S.A.L.F. S.P.A. LABORATORIO FARMACOLOGICO, ITALY

치료 영역:

METOCLOPRAMIDE

치료 징후:

METOCLOPRAMIDE S.A.L.F 10 MG/2 ML is indicated in adults for: - Prevention of postoperative nausea and vomiting (PONV) - Prevention of delayed nausea and vomiting caused by chemotherapy (delayed CINV) - Prevention of nausea and vomiting caused by radiation therapy - Symptomatic treatment of nausea and vomiting, including nausea and vomiting caused by migraine attack. In migraine attacks, metoclopramide can be used concomitantly with oral analgesics to improve their absorption. - Diabetic gastroparesis - To faciliate diagnostic procedures (ie, to faciliate small bowel intubation and as an aid in radiological examinations) Pediatric population. METOCLOPRAMIDE S.A.L.F 10 MG/2 ML is indicated in children aged 1 to 18 years for: - Second line-therapy: Treatment of established postoperative nausea and vomiting (PONV) - Second-line therapy: Prevention of delayed nausea and vomiting caused by chemotherapy (delayed CINV) - To facilitate diagnostic procedures (ie, to faciliate small bowel intubation and as an aid in radiological examinations).

승인 날짜:

2022-04-30

제품 특성 요약

                                SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAME OF THE MEDICINAL PRODUCT
METOCLOPRAMIDE S.A.L.F 10mg/2ml
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 1ml solution contains:
Metoclopramide hydrochloride monohydrate 5.25 mg
(equivalent to 5 mg of Metoclopramide hydrochloride
anhydrous).
Each ampoule of 2ml contains:
Metoclopramide hydrochloride monohydrate 10.5 mg
(equivalent to 10 mg of Metoclopramide
hydrochloride anhydrous).
Excipients with known effect:
Each ampoule of 2ml contains 2.96 mg of sodium
metabisulphite.
Each ampoule of 2ml contains 1.29 mg of sodium.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for I.V or I.M injection.
Clear colorless solution.
4.
CLINICAL PARTICULARS
4.1
Therapeutic indications
Metoclopramide is an antiemetic and stimulates GI
motility.
Adult population
METOCLOPRAMIDE S.A.L.F 10mg/2ml is indicated in
adults for:
-
Prevention of postoperative nausea and vomiting
(PONV).
-
Prevention of delayed nausea and vomiting caused
by chemotherapy (delayed CINV).
-
Prevention of nausea and vomiting caused by
radiation therapy.
-
Symptomatic treatment of nausea and vomiting,
including nausea and vomiting caused by migraine
attack. In migraine attacks, metoclopramide can be
used concomitantly with oral analgesics to improve
their absorption.
-
Diabetic gastroparesis.
-
To facilitate diagnostic procedures (i.e., to facilitate
small bowel intubation and as an aid in radiological
examinations).
Pediatric population
METOCLOPRAMIDE S.A.L.F 10mg/2ml is indicated in
children aged 1 to 18 years for:
-
Second line-therapy: Treatment of established
postoperative nausea and vomiting (PONV).
-
Second-line therapy: Prevention of delayed nausea
and vomiting caused by chemotherapy (delayed
CINV).
-
To facilitate diagnostic procedures (i.e., to facilitate
small bowel intubation and as an aid in radiological
examinations).
4.2
Posology and method of administration
Posology
Adult patients
For all adult indications except diabetic gastroparesis
and facilitation of diagnostic pro
                                
                                전체 문서 읽기
                                
                            

이 제품과 관련된 검색 알림