BRIDION

Ország: Izrael

Nyelv: angol

Forrás: Ministry of Health

Aktív összetevők:

SUGAMMADEX

Beszerezhető a:

MERCK SHARP & DOHME (ISRAEL - 1996) COMPANY LTD, ISRAEL

ATC-kód:

V03AB35

Gyógyszerészeti forma:

SOLUTION FOR INJECTION

Összetétel:

SUGAMMADEX 100 MG/ML

Az alkalmazás módja:

I.V

Recept típusa:

Required

Gyártó:

N.V. ORGANON, THE NETHERLANDS

Terápiás csoport:

SUGAMMADEX

Terápiás terület:

SUGAMMADEX

Terápiás javallatok:

Reversal of neuromuscular blockade induced by rocuronium or vecuronium.

Engedély dátuma:

2014-12-31

Termékjellemzők

Bridion
®
100 mg/mL
S
olution for injection
, IV
Sugammadex
1.
NAME OF THE M
EDICINAL PRODUCT
BRIDION
®
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
1 mL
contains sugammadex sodium
equivalent to 1
00 mg
sugammadex.
Each vial of 2 mL
contains sugammadex sodiu
m equivalent to 200
mg sugammadex.
Excipient(s)
with known effect
Contains up to 9.7 mg/mL
sodium (see section
4.4).
For the full list of excipients, se
e section 6.1.
3. PHARMACEUTICAL FORM
Solut
ion for injection
(injection).
Clea
r and colourless to sl
ightly yellow solution.
The pH is between 7 and 8 and osmolality is between 300 and 500
mOsm/kg.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Reversal of neu
romuscular blo
ckade induced b
y ro
curonium or vecuro
nium.
4.2 POSOLO
GY AND METHOD OF ADMIN
ISTRATION
Posology
Sugammadex should only be administered by, or under the supervision of
an anaesthetist.
The use of an appropriate neuromuscular monito
ring techniq
ue is recommen
ded to monitor
the
recovery of neurom
uscular blockade (see section 4.4).
Th
e recommended dose of sugammadex depends on the level of neuromuscular
blockade to
be reversed.
The recommended dose does not depend on the anaesthetic re
gimen.
Sugam
madex can be u
sed to reverse
dif
ferent levels of ro
curonium or vecur
onium induced
neuromus
cular blockade:
_Adults_
Routine reversal:
A dose of 4
mg/kg sugammadex is recommended if recovery has reached at least 1
-2 post-
tetanic counts (PTC) foll
owing rocuro
nium or vecuro
nium induced bl
ock
ade. Median time to
recovery of the T
4
/T
1
ratio to 0.9 is around 3
minutes (see section
5.1).
A dose of 2
mg/kg sugammadex is recommended, if spontaneous recovery has occurred
up to
at least the reappearance of T
2
following
rocuronium or
vecuronium indu
c
ed blockade.
Median time to recovery of the T
4
/T
1
ratio to 0
.9 is around 2
minutes (see section
5.1).
Using the recommended doses for routine reversal will result in a
slightly faster median time
to recovery of the
T
4
/T
1
ratio to 0.9 of roc
uronium when co
mpared to vecuronium