Zoledronic acid Teva Pharma

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
12-12-2018

Ingredient activ:

zoledronic acid

Disponibil de la:

Teva B.V.

Codul ATC:

M05BA08

INN (nume internaţional):

zoledronic acid

Grupul Terapeutică:

Drugs for treatment of bone diseases

Zonă Terapeutică:

Osteoporosis; Osteitis Deformans; Osteoporosis, Postmenopausal

Indicații terapeutice:

Treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture including those with a recent low-trauma hip fracture. Treatment of osteoporosis associated with long-term systemic glucocorticoid therapy: , in post-menopausal women;, in men; , at increased risk of fracture. Treatment of Paget’s disease of the bone in adults.,

Rezumat produs:

Revision: 11

Statutul autorizaţiei:

Withdrawn

Data de autorizare:

2012-08-15

Prospect

                                53
B. PACKAGE LEAFLET
Medicinal product no longer authorised
54
PACKAGE LEAFLET: INFORMATION FOR THE USER
_ _
ZOLEDRONIC ACID TEVA PHARMA 5 MG SOLUTION FOR INFUSION IN BOTTLES
zoledronic acid
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU ARE GIVEN 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, pharmacist or
nurse.
-
If you get any side effects talk to your doctor, pharmacist or nurse.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Zoledronic acid Teva Pharma is and what it is used for
2.
What you need to know before you are given Zoledronic acid Teva Pharma
3.
How Zoledronic acid Teva Pharma is given
4.
Possible side effects
5.
How to store Zoledronic acid Teva Pharma
6.
Contents of the pack and other information
1.
WHAT ZOLEDRONIC ACID TEVA PHARMA IS AND WHAT IT IS USED FOR
Zoledronic acid Teva Pharma contains the active substance zoledronic
acid. It belongs to a group of
medicines called bisphosphonates and is used to treat post-menopausal
women and adult men with
osteoporosis or osteoporosis caused by treatment with corticosteroids
used to treat inflammation, and
Paget’s disease of the bone in adults.
OSTEOPOROSIS
Osteoporosis is a disease that involves the thinning and weakening of
the bones and is common in
women after the menopause, but can also occur in men. At the
menopause, a woman’s ovaries stop
producing the female hormone oestrogen, which helps keep bones
healthy. Following the menopause
bone loss occurs, bones become weaker and break more easily.
Osteoporosis could also occur in men
and women because of the long term use of steroids, which can affect
the strength of bones. Many
patients with osteoporosis have no symptoms but they are still at risk
of breaking bones because
osteoporosis has made their bones weaker. Decreased circulating levels
of sex hormones, mainly
oestrogens converted from androgens, also 
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Zoledronic acid Teva Pharma 5 mg solution for infusion in bottles
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each bottle with 100 ml of solution contains 5 mg zoledronic acid (as
monohydrate).
Each ml of the solution contains 0.05 mg zoledronic acid (as
monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for infusion.
Clear and colourless solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Treatment of osteoporosis
•
in post-menopausal women
•
in adult men
at increased risk of fracture, including those with a recent
low-trauma hip fracture.
Treatment of osteoporosis associated with long-term systemic
glucocorticoid therapy
•
in post-menopausal women
•
in adult men
at increased risk of fracture.
Treatment of Paget’s disease of the bone in adults.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
Patients must be appropriately hydrated prior to administration of
Zoledronic acid Teva Pharma. This
is especially important for the elderly (≥ 65 years) and for
patients receiving diuretic therapy.
Adequate calcium and vitamin D intake are recommended in association
with Zoledronic acid Teva
Pharma administration.
_Osteoporosis_
For the treatment of post-menopausal osteoporosis, osteoporosis in men
and the treatment of
osteoporosis associated with long-term systemic glucocorticoid
therapy, the recommended dose is a
single intravenous infusion of 5 mg Zoledronic acid Teva Pharma
administered once a year.
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
Zoledronic acid Teva Pharma on an individual patient basis,
particularly after 5 or more years of use.
In patients with a recent low-trauma hip fracture, it is recommended
to give the zoledronic acid
infusion at least two weeks after hip
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului bulgară 12-12-2018
Raport public de evaluare Raport public de evaluare bulgară 12-12-2018
Prospect Prospect spaniolă 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului spaniolă 12-12-2018
Raport public de evaluare Raport public de evaluare spaniolă 12-12-2018
Prospect Prospect cehă 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului cehă 12-12-2018
Raport public de evaluare Raport public de evaluare cehă 12-12-2018
Prospect Prospect daneză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului daneză 12-12-2018
Raport public de evaluare Raport public de evaluare daneză 12-12-2018
Prospect Prospect germană 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului germană 12-12-2018
Raport public de evaluare Raport public de evaluare germană 12-12-2018
Prospect Prospect estoniană 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului estoniană 12-12-2018
Raport public de evaluare Raport public de evaluare estoniană 12-12-2018
Prospect Prospect greacă 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului greacă 12-12-2018
Raport public de evaluare Raport public de evaluare greacă 12-12-2018
Prospect Prospect franceză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului franceză 12-12-2018
Raport public de evaluare Raport public de evaluare franceză 12-12-2018
Prospect Prospect italiană 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului italiană 12-12-2018
Raport public de evaluare Raport public de evaluare italiană 12-12-2018
Prospect Prospect letonă 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului letonă 12-12-2018
Raport public de evaluare Raport public de evaluare letonă 12-12-2018
Prospect Prospect lituaniană 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului lituaniană 12-12-2018
Raport public de evaluare Raport public de evaluare lituaniană 12-12-2018
Prospect Prospect maghiară 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului maghiară 12-12-2018
Raport public de evaluare Raport public de evaluare maghiară 12-12-2018
Prospect Prospect malteză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului malteză 12-12-2018
Raport public de evaluare Raport public de evaluare malteză 12-12-2018
Prospect Prospect olandeză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului olandeză 12-12-2018
Raport public de evaluare Raport public de evaluare olandeză 12-12-2018
Prospect Prospect poloneză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului poloneză 12-12-2018
Raport public de evaluare Raport public de evaluare poloneză 12-12-2018
Prospect Prospect portugheză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului portugheză 12-12-2018
Raport public de evaluare Raport public de evaluare portugheză 12-12-2018
Prospect Prospect română 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului română 12-12-2018
Raport public de evaluare Raport public de evaluare română 12-12-2018
Prospect Prospect slovacă 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului slovacă 12-12-2018
Raport public de evaluare Raport public de evaluare slovacă 12-12-2018
Prospect Prospect slovenă 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului slovenă 12-12-2018
Raport public de evaluare Raport public de evaluare slovenă 12-12-2018
Prospect Prospect finlandeză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului finlandeză 12-12-2018
Raport public de evaluare Raport public de evaluare finlandeză 12-12-2018
Prospect Prospect suedeză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului suedeză 12-12-2018
Raport public de evaluare Raport public de evaluare suedeză 12-12-2018
Prospect Prospect norvegiană 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului norvegiană 12-12-2018
Prospect Prospect islandeză 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului islandeză 12-12-2018
Prospect Prospect croată 12-12-2018
Caracteristicilor produsului Caracteristicilor produsului croată 12-12-2018
Raport public de evaluare Raport public de evaluare croată 12-12-2018

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor