ProQuad

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Bipacksedel Bipacksedel (PIL)
22-07-2022
Produktens egenskaper Produktens egenskaper (SPC)
22-07-2022

Aktiva substanser:

virus, live attenuated, measles, virus, live attenuated, mumps, virus, live attenuated, rubella, virus, live attenuated, varicella

Tillgänglig från:

Merck Sharp & Dohme B.V.

ATC-kod:

J07BD54

INN (International namn):

measles, mumps, rubella and varicella vaccine (live)

Terapeutisk grupp:

Vaccines

Terapiområde:

Chickenpox; Rubella; Measles; Mumps; Immunization

Terapeutiska indikationer:

ProQuad is indicated for simultaneous vaccination against measles, mumps, rubella and varicella in individuals from 12 months of age. ProQuad can be administered to individuals from 9 months of age under special circumstances (e.g., to conform with national vaccination schedules, outbreak situations, or travel to a region with high prevalence of measles.,

Produktsammanfattning:

Revision: 31

Bemyndigande status:

Authorised

Tillstånd datum:

2006-04-05

Bipacksedel

                                38
B. PACKAGE LEAFLET
39
PACKAGE LE
AFLET: INFORMATION FOR THE USER
PROQUAD
POWDER AND SO
LVENT FOR SUSPENSION FOR INJECTION
Measles, mumps, rubella and varicella vac
cine (live)
R
EAD ALL OF THIS LEAFLE
T CAREFULLY BEFORE YOU OR YO
UR CHILD IS VACCINA
TED
BECAUSE IT CONTAINS
IMPORTANT INFORMATI
ON FOR YOU.
-
Keep this leaflet. You may ne
ed to read it again.
-
If you have any further questions, ask your doctor or your pharm
acist.
-
This
vaccine has been presc
ribed for you o
r your child
only. Do not pass i
t on to others.
-
If you get any of the sid
e effects, talk to your doctor or pharmacis
t. This inc
ludes any possible
side effects not listed in this leaflet.
See section 4.
WHAT IS IN THIS LEAFLET
1.
What Pro
Quad is and wha
t it is used for
2.
What you need
to know before you receive ProQuad
3.
How
to use ProQuad
4.
Possible side effects
5.
How to store ProQuad
6.
Contents of the pack and other information
1.
WHAT PROQUAD I
S AND WHAT IT IS USED FOR
ProQuad
is a vaccine co
ntaining meas
les, mumps, rubella,
and chickenpox (varicella) viruses that
h
ave been weakened. When
a person is
given the vaccine, the immune system (the body’s natural
defences
) will make antibodies agains
t the measles,
mumps, rubella, and
varicella viruses. The
antibo
dies help protect against diseases caused by these viruses.
P
roQuad is given to help
protect you
r child against measles, mumps, rubella
, and chickenpox
(varicella)
. The vaccine may be adminis
tered to perso
ns from 12 months of
age.
ProQuad ma
y also be adm
inistered to infants from 9 months of age under special circum
stances (to
co
nform with national vaccination schedules, outbreak situatio
ns, or travel to a
region with high
prevalence of measle
s).
Although
ProQuad contains liv
e
viruses, they a
re too weak t
o cause measles, mumps, rubella, or
chickenpox (varicella) in
healthy people.
2.
WHAT YOU NEED TO KNOW BEFORE YOU
RECEIVE PROQUAD
DO
NOT USE PROQUAD

If the person to be vaccinated is aller
gic to any varicella
vaccine or mea
sles, mumps, or rubella
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                1
ANNEX I
SUMMARY
OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
ProQuad powder and solvent for suspension for injection
ProQuad powder and solvent for suspension for
injection in a pre-filled syringe
Measles, mump
s,
rubella and varicella vaccin
e (live).
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
After reconstitution, one dose (0.5
mL) contains:
Measles virus
1
Enders’ Edmonston strain (live, attenuated)
........ not less than 3.00 log
10
TCID
50
*
Mumps virus
1
Jeryl Lynn
™
(Le
vel B) strain (live, attenua
ted) ...
not less than 4.30 log
10
TCID
50
*
Rubella virus
2
Wistar RA 27/3 strain (live, attenuated)
...............
not less than 3.00 log
10
TCID
50
*
Varicella virus
3
Oka/Merck strain (live, attenuat
ed) ...................
not less than 3.99 log
10
PFU**
*50% tissue cultur
e infectious dose
**plaque-f
orming units
(
1
) Produced in chick embryo cells.
(
2
) Produced in human diploid lung (WI
-38) fibroblasts.
(
3
) Produced in human diploid (MRC
-5) cells.
The vaccine may contain
traces of recombinant human alb
umin (rHA).
This vacc
ine contains a trace amount
of neomycin. See section 4.3.
Excipient(s)
with known effect
The vaccine contains 16
milligrams
of sorbitol per dose.
See section 4.4.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder and solve
nt for suspension for injection
Before r
econstitution, the pow
der is a white to pale yellow
compact
crystalline cake and the solvent is
a clear colourless liquid.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
ProQuad is indicated for simultaneous
vaccination against measles, mumps, rub
ella and varicella in
individuals from 12
months of age.
ProQuad
can be administered to individuals from 9
months of
age under special circumstances (e.g.,
to conform with national vaccination sche
dules, outbreak
situations, or travel to a region with hig
h
prevalence of measle
s; see sections 4.2, 4.4, and
5.1).
3
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
ProQu
ad should be used in accordance to official r
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 22-07-2022
Produktens egenskaper Produktens egenskaper bulgariska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 08-10-2020
Bipacksedel Bipacksedel spanska 22-07-2022
Produktens egenskaper Produktens egenskaper spanska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 08-10-2020
Bipacksedel Bipacksedel tjeckiska 22-07-2022
Produktens egenskaper Produktens egenskaper tjeckiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 08-10-2020
Bipacksedel Bipacksedel danska 22-07-2022
Produktens egenskaper Produktens egenskaper danska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 08-10-2020
Bipacksedel Bipacksedel tyska 22-07-2022
Produktens egenskaper Produktens egenskaper tyska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 08-10-2020
Bipacksedel Bipacksedel estniska 22-07-2022
Produktens egenskaper Produktens egenskaper estniska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 08-10-2020
Bipacksedel Bipacksedel grekiska 22-07-2022
Produktens egenskaper Produktens egenskaper grekiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 08-10-2020
Bipacksedel Bipacksedel franska 22-07-2022
Produktens egenskaper Produktens egenskaper franska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 08-10-2020
Bipacksedel Bipacksedel italienska 22-07-2022
Produktens egenskaper Produktens egenskaper italienska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 08-10-2020
Bipacksedel Bipacksedel lettiska 22-07-2022
Produktens egenskaper Produktens egenskaper lettiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 08-10-2020
Bipacksedel Bipacksedel litauiska 22-07-2022
Produktens egenskaper Produktens egenskaper litauiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 08-10-2020
Bipacksedel Bipacksedel ungerska 22-07-2022
Produktens egenskaper Produktens egenskaper ungerska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 08-10-2020
Bipacksedel Bipacksedel maltesiska 22-07-2022
Produktens egenskaper Produktens egenskaper maltesiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 08-10-2020
Bipacksedel Bipacksedel nederländska 22-07-2022
Produktens egenskaper Produktens egenskaper nederländska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 08-10-2020
Bipacksedel Bipacksedel polska 22-07-2022
Produktens egenskaper Produktens egenskaper polska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 08-10-2020
Bipacksedel Bipacksedel portugisiska 22-07-2022
Produktens egenskaper Produktens egenskaper portugisiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 08-10-2020
Bipacksedel Bipacksedel rumänska 22-07-2022
Produktens egenskaper Produktens egenskaper rumänska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 08-10-2020
Bipacksedel Bipacksedel slovakiska 22-07-2022
Produktens egenskaper Produktens egenskaper slovakiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 08-10-2020
Bipacksedel Bipacksedel slovenska 22-07-2022
Produktens egenskaper Produktens egenskaper slovenska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 08-10-2020
Bipacksedel Bipacksedel finska 22-07-2022
Produktens egenskaper Produktens egenskaper finska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 08-10-2020
Bipacksedel Bipacksedel svenska 22-07-2022
Produktens egenskaper Produktens egenskaper svenska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 08-10-2020
Bipacksedel Bipacksedel norska 22-07-2022
Produktens egenskaper Produktens egenskaper norska 22-07-2022
Bipacksedel Bipacksedel isländska 22-07-2022
Produktens egenskaper Produktens egenskaper isländska 22-07-2022
Bipacksedel Bipacksedel kroatiska 22-07-2022
Produktens egenskaper Produktens egenskaper kroatiska 22-07-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport kroatiska 08-10-2020

Visa dokumenthistorik