Adrovance

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

colecalciferol, alendronic acid (as sodium trihydrate)

Available from:

N.V. Organon

ATC code:

M05BB03

INN (International Name):

alendronic acid, colecalciferol

Therapeutic group:

Drugs for treatment of bone diseases

Therapeutic area:

Osteoporosis, Postmenopausal

Therapeutic indications:

Treatment of postmenopausal osteoporosis in patients at risk of vitamin-D insufficiency.Adrovance reduces the risk of vertebral and hip fractures.

Product summary:

Revision: 25

Authorization status:

Authorised

Authorization date:

2007-01-04

Patient Information leaflet

                                28
B. PACKAGE LEAFLET
29
PACKAGE LEAFLET: INFORMATION FOR THE USER
ADROVANCE 70 MG/2,800 IU TABLETS
ADROVANCE 70 MG/5,600 IU TABLETS
alendronic acid/colecalciferol
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, ask your doctor or pharmacist.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
-
If you get any side effects talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
-
It is particularly important to understand the information in section
3 before taking this
medicine.
WHAT IS IN THIS LEAFLET
1.
What ADROVANCE is and what it is used for
2.
What you need to know before you take ADROVANCE
3.
How to take ADROVANCE
4.
Possible side effects
5
How to store ADROVANCE
6.
Contents of the pack and other information
1.
WHAT ADROVANCE IS AND WHAT IT IS USED FOR
WHAT IS ADROVANCE?
ADROVANCE is a tablet containing the two active substances, alendronic
acid (commonly called
alendronate) and colecalciferol known as vitamin D
3
.
WHAT IS ALENDRONATE?
Alendronate belongs to a group of non-hormonal medicines called
bisphosphonates. Alendronate
prevents the loss of bone that occurs in women after they have been
through the menopause, and helps
to rebuild bone. It reduces the risk of spine and hip fractures.
WHAT IS VITAMIN D?
Vitamin D is an essential nutrient, required for calcium absorption
and healthy bones. The body can
only absorb calcium properly from our food if it has enough vitamin D.
Very few foods contain
vitamin D. The main source is through exposure to summer sunlight,
which makes vitamin D in our
skin. As we get older our skin makes less vitamin D. Too little
vitamin D may lead to bone loss and
osteoporosis. Severe vitamin D deficiency may cause muscle weakness
which can lead to falls and 
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
ADROVANCE 70 mg/2,800 IU tablets
ADROVANCE 70 mg/5,600 IU tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
ADROVANCE 70 mg/2,800 IU tablets
Each tablet contains 70 mg alendronic acid (as sodium trihydrate) and
70 micrograms (2,800 IU)
colecalciferol (vitamin D
3
).
_Excipients with known effect_
Each tablet contains 62 mg lactose (as lactose anhydrous) and 8 mg
sucrose.
ADROVANCE 70 mg/5,600 IU tablets
Each tablet contains 70 mg alendronic acid (as sodium trihydrate) and
140 micrograms (5,600 IU)
colecalciferol (vitamin D
3
).
_Excipients with known effect _
Each tablet contains 63 mg lactose (as lactose anhydrous) and 16 mg
sucrose.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet
ADROVANCE 70 mg/2,800 IU tablets
Modified capsule-shaped, white to off-white tablets, marked with an
outline of a bone image on one
side, and '710' on the other.
ADROVANCE 70 mg/5,600 IU tablets
Modified rectangle-shaped, white to off-white tablets, marked with an
outline of a bone image on one
side, and '270' on the other.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
ADROVANCE is indicated for the treatment of postmenopausal
osteoporosis in women at risk of
vitamin D insufficiency. It reduces the risk of vertebral and hip
fractures.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_ _
The recommended dose is one tablet once weekly.
Patients should be instructed that if they miss a dose of ADROVANCE
they should take one tablet on
the morning after they remember. They should not take two tablets on
the same day but should return
to taking one tablet once a week, as originally scheduled on their
chosen day.
Due to the nature of the disease process in osteoporosis, ADROVANCE is
intended for long-term use.
3
The optimal duration of bisphosphonate treatment for osteoporosis has
not been established. The need
for continued treatment should be re-evaluated periodically based on
the benefits and potential risks of
ADROVANC
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 20-02-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 20-02-2024
Public Assessment Report Public Assessment Report Bulgarian 19-05-2011
Patient Information leaflet Patient Information leaflet Spanish 20-02-2024
Public Assessment Report Public Assessment Report Spanish 19-05-2011
Patient Information leaflet Patient Information leaflet Czech 20-02-2024
Public Assessment Report Public Assessment Report Czech 19-05-2011
Patient Information leaflet Patient Information leaflet Danish 20-02-2024
Public Assessment Report Public Assessment Report Danish 19-05-2011
Patient Information leaflet Patient Information leaflet German 20-02-2024
Public Assessment Report Public Assessment Report German 19-05-2011
Patient Information leaflet Patient Information leaflet Estonian 20-02-2024
Public Assessment Report Public Assessment Report Estonian 19-05-2011
Patient Information leaflet Patient Information leaflet Greek 20-02-2024
Public Assessment Report Public Assessment Report Greek 19-05-2011
Patient Information leaflet Patient Information leaflet French 20-02-2024
Public Assessment Report Public Assessment Report French 19-05-2011
Patient Information leaflet Patient Information leaflet Italian 20-02-2024
Public Assessment Report Public Assessment Report Italian 19-05-2011
Patient Information leaflet Patient Information leaflet Latvian 20-02-2024
Public Assessment Report Public Assessment Report Latvian 19-05-2011
Patient Information leaflet Patient Information leaflet Lithuanian 20-02-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 20-02-2024
Public Assessment Report Public Assessment Report Lithuanian 19-05-2011
Patient Information leaflet Patient Information leaflet Hungarian 20-02-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 20-02-2024
Public Assessment Report Public Assessment Report Hungarian 19-05-2011
Patient Information leaflet Patient Information leaflet Maltese 20-02-2024
Public Assessment Report Public Assessment Report Maltese 19-05-2011
Patient Information leaflet Patient Information leaflet Dutch 20-02-2024
Public Assessment Report Public Assessment Report Dutch 19-05-2011
Patient Information leaflet Patient Information leaflet Polish 20-02-2024
Public Assessment Report Public Assessment Report Polish 19-05-2011
Patient Information leaflet Patient Information leaflet Portuguese 20-02-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 20-02-2024
Public Assessment Report Public Assessment Report Portuguese 19-05-2011
Patient Information leaflet Patient Information leaflet Romanian 20-02-2024
Public Assessment Report Public Assessment Report Romanian 19-05-2011
Patient Information leaflet Patient Information leaflet Slovak 20-02-2024
Public Assessment Report Public Assessment Report Slovak 19-05-2011
Patient Information leaflet Patient Information leaflet Slovenian 20-02-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 20-02-2024
Public Assessment Report Public Assessment Report Slovenian 19-05-2011
Patient Information leaflet Patient Information leaflet Finnish 20-02-2024
Public Assessment Report Public Assessment Report Finnish 19-05-2011
Patient Information leaflet Patient Information leaflet Swedish 20-02-2024
Public Assessment Report Public Assessment Report Swedish 19-05-2011
Patient Information leaflet Patient Information leaflet Norwegian 20-02-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 20-02-2024
Patient Information leaflet Patient Information leaflet Icelandic 20-02-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 20-02-2024
Patient Information leaflet Patient Information leaflet Croatian 20-02-2024

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