Efficib

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

sitagliptin, metformin hydrochloride

Available from:

Merck Sharp and Dohme B.V

ATC code:

A10BD07

INN (International Name):

sitagliptin, metformin

Therapeutic group:

Drugs used in diabetes

Therapeutic area:

Diabetes Mellitus, Type 2

Therapeutic indications:

For patients with type-2 diabetes mellitus:Efficib is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin.Efficib is indicated in combination with a sulphonylurea (i.e. triple combination therapy) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a sulphonylurea.Efficib is indicated as triple combination therapy with a PPAR agonist (i.e. a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a PPAR agonist.Efficib is also indicated as add on to insulin (i.e., triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dosage of insulin and metformin alone do not provide adequate glycaemic control.

Product summary:

Revision: 33

Authorization status:

Authorised

Authorization date:

2008-07-15

Patient Information leaflet

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDI
CINAL PRODUCT
Efficib 50 mg/850 mg film-
coated tablets
Efficib 50 mg/1,000 mg film-
coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Efficib 50 mg/850 mg film-coated tablets
Each tablet contains sitagliptin phosphate monohydrate
equivalent to 50
mg of sitagliptin and 850
mg
of metf
ormin hydrochloride.
Efficib 50 mg/1,000 mg film-coated tablets
Each tablet contains sitagliptin phosphate monohydrate
equivalent to 50
mg of sitagliptin and
1,000 mg of metf
ormin hydrochloride.
For the full list of
excipients, see section
6.1.
3.
PHARMACEUTICAL
FORM
Film-
coated tablet (tablet).
Efficib 50 mg/850 mg film-coated tablets
Capsule-sh
aped, pink film
-coated tablet with
“515” debossed on one side.
Efficib 50 mg/1,000 mg film-coated tablets
Capsule-shaped, red film-
coated tablet with “
577
” debossed on one side
.
4.
CLINICA
L PARTICULARS
4.1
THERAPEUTIC INDICATIONS
For adult
patients with type
2 diabetes mellitus:
Efficib
is indicated as an adjunct to diet and exercise to improve glycaemic
contro
l in patients
inadequately controlled on their maximal tolerated dose of met
fo
rmin alone or those already being
treated with the combination of
sitagliptin and
metformin.
Efficib
is indicated in combination with a sulphonylurea (i.e., triple
combination t
herapy) as an
adjunct to diet and exercise in patients inadequately controll
ed
on their maximal tolerated dose of
metformin and a s
u
lphonylurea.
Efficib
is indicated as tr
iple
combination therapy with a
peroxisome proliferator
-
activated receptor
gamma (PPAR

) agonist
(i.e., a thiazolidinedione) as an adjunct to diet and exercise
in patients
inadequately controlled on their maximal to
l
erated dose of metformin and a PPAR

agonist.
Efficib is also indicated as add
-
on to insulin (i.e., triple combination ther
apy) a
s an adjunct to diet and
exercise to improve glycaemic control in pati
en
ts when stable
dose
of insulin and metformin alone do
not provide adequate glycaemic contro
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDI
CINAL PRODUCT
Efficib 50 mg/850 mg film-
coated tablets
Efficib 50 mg/1,000 mg film-
coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Efficib 50 mg/850 mg film-coated tablets
Each tablet contains sitagliptin phosphate monohydrate
equivalent to 50
mg of sitagliptin and 850
mg
of metf
ormin hydrochloride.
Efficib 50 mg/1,000 mg film-coated tablets
Each tablet contains sitagliptin phosphate monohydrate
equivalent to 50
mg of sitagliptin and
1,000 mg of metf
ormin hydrochloride.
For the full list of
excipients, see section
6.1.
3.
PHARMACEUTICAL
FORM
Film-
coated tablet (tablet).
Efficib 50 mg/850 mg film-coated tablets
Capsule-sh
aped, pink film
-coated tablet with
“515” debossed on one side.
Efficib 50 mg/1,000 mg film-coated tablets
Capsule-shaped, red film-
coated tablet with “
577
” debossed on one side
.
4.
CLINICA
L PARTICULARS
4.1
THERAPEUTIC INDICATIONS
For adult
patients with type
2 diabetes mellitus:
Efficib
is indicated as an adjunct to diet and exercise to improve glycaemic
contro
l in patients
inadequately controlled on their maximal tolerated dose of met
fo
rmin alone or those already being
treated with the combination of
sitagliptin and
metformin.
Efficib
is indicated in combination with a sulphonylurea (i.e., triple
combination t
herapy) as an
adjunct to diet and exercise in patients inadequately controll
ed
on their maximal tolerated dose of
metformin and a s
u
lphonylurea.
Efficib
is indicated as tr
iple
combination therapy with a
peroxisome proliferator
-
activated receptor
gamma (PPAR

) agonist
(i.e., a thiazolidinedione) as an adjunct to diet and exercise
in patients
inadequately controlled on their maximal to
l
erated dose of metformin and a PPAR

agonist.
Efficib is also indicated as add
-
on to insulin (i.e., triple combination ther
apy) a
s an adjunct to diet and
exercise to improve glycaemic control in pati
en
ts when stable
dose
of insulin and metformin alone do
not provide adequate glycaemic contro
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 07-09-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 07-09-2023
Public Assessment Report Public Assessment Report Bulgarian 05-07-2013
Patient Information leaflet Patient Information leaflet Spanish 07-09-2023
Public Assessment Report Public Assessment Report Spanish 05-07-2013
Patient Information leaflet Patient Information leaflet Czech 07-09-2023
Public Assessment Report Public Assessment Report Czech 05-07-2013
Patient Information leaflet Patient Information leaflet Danish 07-09-2023
Public Assessment Report Public Assessment Report Danish 05-07-2013
Patient Information leaflet Patient Information leaflet German 07-09-2023
Public Assessment Report Public Assessment Report German 05-07-2013
Patient Information leaflet Patient Information leaflet Estonian 07-09-2023
Public Assessment Report Public Assessment Report Estonian 05-07-2013
Patient Information leaflet Patient Information leaflet Greek 07-09-2023
Public Assessment Report Public Assessment Report Greek 05-07-2013
Patient Information leaflet Patient Information leaflet French 07-09-2023
Public Assessment Report Public Assessment Report French 05-07-2013
Patient Information leaflet Patient Information leaflet Italian 07-09-2023
Public Assessment Report Public Assessment Report Italian 05-07-2013
Patient Information leaflet Patient Information leaflet Latvian 07-09-2023
Public Assessment Report Public Assessment Report Latvian 05-07-2013
Patient Information leaflet Patient Information leaflet Lithuanian 07-09-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 07-09-2023
Public Assessment Report Public Assessment Report Lithuanian 05-07-2013
Patient Information leaflet Patient Information leaflet Hungarian 07-09-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 07-09-2023
Public Assessment Report Public Assessment Report Hungarian 05-07-2013
Patient Information leaflet Patient Information leaflet Maltese 07-09-2023
Public Assessment Report Public Assessment Report Maltese 05-07-2013
Patient Information leaflet Patient Information leaflet Dutch 07-09-2023
Public Assessment Report Public Assessment Report Dutch 05-07-2013
Patient Information leaflet Patient Information leaflet Polish 07-09-2023
Public Assessment Report Public Assessment Report Polish 05-07-2013
Patient Information leaflet Patient Information leaflet Portuguese 07-09-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 07-09-2023
Public Assessment Report Public Assessment Report Portuguese 05-07-2013
Patient Information leaflet Patient Information leaflet Romanian 07-09-2023
Public Assessment Report Public Assessment Report Romanian 05-07-2013
Patient Information leaflet Patient Information leaflet Slovak 07-09-2023
Public Assessment Report Public Assessment Report Slovak 05-07-2013
Patient Information leaflet Patient Information leaflet Slovenian 07-09-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 07-09-2023
Public Assessment Report Public Assessment Report Slovenian 05-07-2013
Patient Information leaflet Patient Information leaflet Finnish 07-09-2023
Public Assessment Report Public Assessment Report Finnish 05-07-2013
Patient Information leaflet Patient Information leaflet Swedish 07-09-2023
Public Assessment Report Public Assessment Report Swedish 05-07-2013
Patient Information leaflet Patient Information leaflet Norwegian 07-09-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 07-09-2023
Patient Information leaflet Patient Information leaflet Icelandic 07-09-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 07-09-2023
Patient Information leaflet Patient Information leaflet Croatian 07-09-2023

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