Invanz

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

ertapenem sodium

Available from:

Merck Sharp & Dohme B.V.

ATC code:

J01DH03

INN (International Name):

ertapenem

Therapeutic group:

Antibacterials for systemic use,

Therapeutic area:

Community-Acquired Infections; Streptococcal Infections; Staphylococcal Infections; Gram-Negative Bacterial Infections; Surgical Wound Infection; Pneumonia, Bacterial

Therapeutic indications:

TreatmentTreatment of the following infections when caused by bacteria known or very likely to be susceptible to ertapenem and when parenteral therapy is required:intra-abdominal infections;community-acquired pneumonia;acute gynaecological infections;diabetic foot infections of the skin and soft tissue.PreventionInvanz is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery.Consideration should be given to official guidance on the appropriate use of antibacterial agents.

Product summary:

Revision: 26

Authorization status:

Authorised

Authorization date:

2002-04-18

Patient Information leaflet

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
INVANZ 1
g powder for concentrate for solution for infusion
2.
QUALITATIVE AND QUAN
T
ITATIVE COMPOSITION
Each vial contains 1.0
g ertapenem.
Excipient(s)
with known
effect
Each 1.0
g dose contains approximately 6.0
mEq of sodium (approximately 137
mg).
For the
full list of excipients,
see section 6.1.
3.
PHA
RMACEUTICAL FORM
Powder fo
r concentrate for solution for infusion.
White to off-white powder.
4.
CLINICA
L PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Treatment
INVANZ is indicated in paediatri
c patients (3
months to 17
years of age
) and in adults for t
he
treatment of the follow
i
ng infections when caused by bacteria kno
wn or very likely to be susceptible
to e
rtapenem and w
hen parenteral therapy is required (see sections
4.4 and 5.1):

Intra-abdo
minal infections

Community acquired pneumonia

Acute gynaecol
ogical infections

Diabetic
foot infections of the skin and soft tiss
ue (see section 4.4)
Prevention
INVANZ is indicated
in adults for the prophylaxis of surgical site infection following
electiv
e
colorectal surgery
(see section 4.4).
Consideration shoul
d be given to official gui
d
ance on the appropriate use of antibacter
ial agents.
4.2
POSOLOGY AND METHOD OF
ADMINISTRATION
Posology
Treatment
Adults and adolescents (13
to 17 years of age): The
dose of INVANZ is 1
gram (g) given once a day
by the intrave
nous route (
see section
6.6).
Infants and children (3
months to 12 years of age): The dose of INVANZ is 15
mg/kg given tw
ice
daily (not to exceed 1
g/day) by the intravenous route (see section
6.6).
3
Prevention
Adults:
To prevent surgical site infections
following elective colore
ctal surgery
, the recommended
dosage is 1 g administered as a single intravenous d
ose to be comp
leted within 1
hour prior to the
surgical incision.
Paediatric population
The safety and efficacy of INVANZ in children below 3
month
s of age have not yet been
established.
No data are available.
Renal impairment
INVANZ may be us
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
INVANZ 1
g powder for concentrate for solution for infusion
2.
QUALITATIVE AND QUAN
T
ITATIVE COMPOSITION
Each vial contains 1.0
g ertapenem.
Excipient(s)
with known
effect
Each 1.0
g dose contains approximately 6.0
mEq of sodium (approximately 137
mg).
For the
full list of excipients,
see section 6.1.
3.
PHA
RMACEUTICAL FORM
Powder fo
r concentrate for solution for infusion.
White to off-white powder.
4.
CLINICA
L PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Treatment
INVANZ is indicated in paediatri
c patients (3
months to 17
years of age
) and in adults for t
he
treatment of the follow
i
ng infections when caused by bacteria kno
wn or very likely to be susceptible
to e
rtapenem and w
hen parenteral therapy is required (see sections
4.4 and 5.1):

Intra-abdo
minal infections

Community acquired pneumonia

Acute gynaecol
ogical infections

Diabetic
foot infections of the skin and soft tiss
ue (see section 4.4)
Prevention
INVANZ is indicated
in adults for the prophylaxis of surgical site infection following
electiv
e
colorectal surgery
(see section 4.4).
Consideration shoul
d be given to official gui
d
ance on the appropriate use of antibacter
ial agents.
4.2
POSOLOGY AND METHOD OF
ADMINISTRATION
Posology
Treatment
Adults and adolescents (13
to 17 years of age): The
dose of INVANZ is 1
gram (g) given once a day
by the intrave
nous route (
see section
6.6).
Infants and children (3
months to 12 years of age): The dose of INVANZ is 15
mg/kg given tw
ice
daily (not to exceed 1
g/day) by the intravenous route (see section
6.6).
3
Prevention
Adults:
To prevent surgical site infections
following elective colore
ctal surgery
, the recommended
dosage is 1 g administered as a single intravenous d
ose to be comp
leted within 1
hour prior to the
surgical incision.
Paediatric population
The safety and efficacy of INVANZ in children below 3
month
s of age have not yet been
established.
No data are available.
Renal impairment
INVANZ may be us
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 25-10-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 25-10-2022
Public Assessment Report Public Assessment Report Bulgarian 02-12-2016
Patient Information leaflet Patient Information leaflet Spanish 25-10-2022
Public Assessment Report Public Assessment Report Spanish 02-12-2016
Patient Information leaflet Patient Information leaflet Czech 25-10-2022
Public Assessment Report Public Assessment Report Czech 02-12-2016
Patient Information leaflet Patient Information leaflet Danish 25-10-2022
Public Assessment Report Public Assessment Report Danish 02-12-2016
Patient Information leaflet Patient Information leaflet German 25-10-2022
Public Assessment Report Public Assessment Report German 02-12-2016
Patient Information leaflet Patient Information leaflet Estonian 25-10-2022
Public Assessment Report Public Assessment Report Estonian 02-12-2016
Patient Information leaflet Patient Information leaflet Greek 25-10-2022
Public Assessment Report Public Assessment Report Greek 02-12-2016
Patient Information leaflet Patient Information leaflet French 25-10-2022
Public Assessment Report Public Assessment Report French 02-12-2016
Patient Information leaflet Patient Information leaflet Italian 25-10-2022
Public Assessment Report Public Assessment Report Italian 02-12-2016
Patient Information leaflet Patient Information leaflet Latvian 25-10-2022
Public Assessment Report Public Assessment Report Latvian 02-12-2016
Patient Information leaflet Patient Information leaflet Lithuanian 25-10-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 25-10-2022
Public Assessment Report Public Assessment Report Lithuanian 02-12-2016
Patient Information leaflet Patient Information leaflet Hungarian 25-10-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 25-10-2022
Public Assessment Report Public Assessment Report Hungarian 02-12-2016
Patient Information leaflet Patient Information leaflet Maltese 25-10-2022
Public Assessment Report Public Assessment Report Maltese 02-12-2016
Patient Information leaflet Patient Information leaflet Dutch 25-10-2022
Public Assessment Report Public Assessment Report Dutch 02-12-2016
Patient Information leaflet Patient Information leaflet Polish 25-10-2022
Public Assessment Report Public Assessment Report Polish 02-12-2016
Patient Information leaflet Patient Information leaflet Portuguese 25-10-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 25-10-2022
Public Assessment Report Public Assessment Report Portuguese 02-12-2016
Patient Information leaflet Patient Information leaflet Romanian 25-10-2022
Public Assessment Report Public Assessment Report Romanian 02-12-2016
Patient Information leaflet Patient Information leaflet Slovak 25-10-2022
Public Assessment Report Public Assessment Report Slovak 02-12-2016
Patient Information leaflet Patient Information leaflet Slovenian 25-10-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 25-10-2022
Public Assessment Report Public Assessment Report Slovenian 02-12-2016
Patient Information leaflet Patient Information leaflet Finnish 25-10-2022
Public Assessment Report Public Assessment Report Finnish 02-12-2016
Patient Information leaflet Patient Information leaflet Swedish 25-10-2022
Public Assessment Report Public Assessment Report Swedish 02-12-2016
Patient Information leaflet Patient Information leaflet Norwegian 25-10-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 25-10-2022
Patient Information leaflet Patient Information leaflet Icelandic 25-10-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 25-10-2022
Patient Information leaflet Patient Information leaflet Croatian 25-10-2022
Public Assessment Report Public Assessment Report Croatian 02-12-2016

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