Flumazenil 500micrograms/5ml solution for injection ampoules

国: イギリス

言語: 英語

ソース: MHRA (Medicines & Healthcare Products Regulatory Agency)

即購入

製品の特徴 製品の特徴 (SPC)
20-06-2018

有効成分:

Flumazenil

から入手可能:

Actavis UK Ltd

ATCコード:

V03AB25

INN(国際名):

Flumazenil

投薬量:

100microgram/1ml

医薬品形態:

Solution for injection

投与経路:

Intravenous

クラス:

No Controlled Drug Status

処方タイプ:

Valid as a prescribable product

製品概要:

BNF: 15010700; GTIN: 5012617022479

情報リーフレット

                                Flumazenil 0.5mg/5ml PIL - UK
item no: AAAC7774
print proof no: 2
origination date: 02.11.11
originated by: SA
revision date: 15.11.11
revised by: sa
dimensions: 148x570
pharmacode:
colours/plates:
approved for print/date
Non Printing Colours
1. Black
2.
3.
4.
5.
6.
1.
2.
3.
date sent: 07.11.11
supplier: Synthon
technically app. date: 15.11.11
min pt size:
TECHNICAL APPROVAL
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING
THIS MEDICINE.
t
,FFQUIJTMFBøFU:PVNBZOFFEUPSFBEJUBHBJO
t
*GZPVIBWFBOZGVSUIFSRVFTUJPOT BTLZPVSEPDUPSPS
QIBSNBDJTU
t
5IJTNFEJDJOFIBTCFFOQSFTDSJCFEGPSZPV%POPUQBTT
JUPOUPPUIFST*UNBZIBSNUIFN FWFOJGUIFJSTZNQUPNT
BSFUIFTBNFBTZPVST
t
*GBOZPGUIFTJEFFòFDUTHFUTTFSJPVT PSJGZPVOPUJDFBOZ
TJEFFòFDUTOPUMJTUFEJOUIJTMFBøFU QMFBTFUFMMZPVSEPDUPS
PSQIBSNBDJTU
t
5IFOBNFPGZPVSNFEJDJOFJT'MVNB[FOJMTPMVUJPOGPS
JOKFDUJPO XIJDIXJMMCFSFGFSSFEUPBTA'MVNB[FOJMPS
A'MVNB[FOJMNHNM4PMVUJPOGPS*OKFDUJPOUISPVHIPVU
UIJTMFBøFU
IN THIS LEAFLET:
1 WHAT FLUMAZENIL 0.1MG/ML SOLUTION
FOR INJECTION IS AND WHAT IT IS USED FOR
2 BEFORE YOU USE
3 HOW YOU USE
4 POSSIBLE SIDE EFFECTS
5 HOW TO STORE
6 FURTHER INFORMATION
1 WHAT FLUMAZENIL 0.1MG/ML SOLUTION FOR INJECTION IS
AND WHAT IT IS USED FOR
'MVNB[FOJMNHNM4PMVUJPOGPS*OKFDUJPODPOUBJOTUIFBDUJWFJOHSFEJFOU
øVNB[FOJM'MVNB[FOJMCFMPOHTUPBHSPVQPGNFEJDJOFTLOPXOBT
CFO[PEJB[FQJOFBOUBHPOJTUT
'MVNB[FOJMJTVTFEUPSFWFSTFUIFFòFDUTPGBHSPVQPGNFEJDJOFTLOPXO
BTCFO[PEJB[FQJOFT
XIJDIBSFVTFEUPDBVTFEFFQTMFFQ#ZSFWFSTJOHUIF
FòFDUTPGCFO[PEJB[FQJOFT
JUBMMPXTUIFQBUJFOUUPCFDPNFDPOTDJPVTTP
UIBUUIFZDBOCSFBUIFVOBJEFE
'MVNB[FOJMDBOCFVTFEUPQBSUMZPSDPNQMFUFMZSFWFSTFUIFFòFDUTPG
CFO[PEJB[FQJOFTFEBUJPOBOEHFOFSBMBOBFTUIFTJBBGUFSNFEJDBMUFTUTBOE
PQFSBUJPOTJOUIFIPTQJUBM*UJTVTFEPOJOUFOTJWFDBSFQBUJFOUTUPCSJOH
BCPVUVOBJEFECSFBUIJOH*UJTBMTPVTFEUPEJBHOPTFBOEUSFBUQBUJFOUT
XIPIBWFCFFO
                                
                                完全なドキュメントを読む
                                
                            

製品の特徴

                                OBJECT 1
FLUMAZENIL 0.1 MG/ML SOLUTION FOR INJECTION
Summary of Product Characteristics Updated 28-Jun-2012 | Accord-UK Ltd
1. Name of the medicinal product
Flumazenil 0.1 mg/ml solution for injection.
2. Qualitative and quantitative composition
Each ml contains 0.1 mg flumazenil.
1 ampoule with 5 ml contains 0.5 mg flumazenil.
1 ampoule with 10 ml contains 1 mg flumazenil.
Excipient: each ml of solution contains 3.8 mg sodium.
For a full list of excipients, see section 6.1.
3. Pharmaceutical form
Solution for injection.
Clear colourless solution.
4. Clinical particulars
4.1 Therapeutic indications
Flumazenil is indicated for the complete or partial reversal of the
central sedative effects of
benzodiazepines. It may therefore be used in anaesthesia and in the
intensive care in the following
situations:
_In anaesthesia_
- Termination of hypnosedative effects in general anaesthesia induced
and/or maintained with
benzodiazepines in hospitalized patients.
- Reversal of benzodiazepine sedation in short-term diagnostic and
therapeutic procedures in ambulatory
patients and hospitalized patients.
_In intensive care situations_
- For the specific reversal of the central effects of benzodiazepines,
in order to restore spontaneous
respiration.
- For diagnosis and treatment of intoxications or overdose with only
or mainly benzodiazepines.
For the reversal of conscious sedation induced with benzodiazepines in
children > 1 year of age.
4.2 Posology and method of administration
Flumazenil must be administered intravenously by an anaesthesist or
doctor with experience in
anesthesiology. Flumazenil may be administered either undiluted or
diluted.
For dilution, see section 6.6.
It can be administered together with other reanimation measures.
Adults
_Anaesthesia_
The initial dose is 0.2 mg administered i.v. in 15 seconds. If the
desired degree of consciousness is not
obtained within 60 seconds, a second dose of 0.1 mg can be
administered. This may be repeated at 60-
second intervals where necessary, up to a total dose of 1.0 mg. Th
                                
                                完全なドキュメントを読む
                                
                            

この製品に関連するアラートを検索