Zoledronic Acid Accord

Krajina: Európska únia

Jazyk: angličtina

Zdroj: EMA (European Medicines Agency)

Aktívna zložka:

zoledronic acid monohydrate

Dostupné z:

Accord Healthcare S.L.U.

ATC kód:

M05BA08

INN (Medzinárodný Name):

zoledronic acid

Terapeutické skupiny:

Bisphosphonates

Terapeutické oblasti:

Hypercalcemia; Fractures, Bone; Cancer

Terapeutické indikácie:

Prevention of skeletal related events (pathological fractures, spinal compression, radiation or surgery to bone, or tumour-induced hypercalcaemia) in adult patients with advanced malignancies involving bone.Treatment of adult patients with tumour-induced hypercalcaemia (TIH).

Prehľad produktov:

Revision: 9

Stav Autorizácia:

Authorised

Dátum Autorizácia:

2014-01-16

Príbalový leták

26
B. PACKAGE LEAFLET
27
PACKAGE LEAFLET: INFORMATION FOR THE USER
ZOLEDRONIC ACID ACCORD 4 MG/5 ML CONCENTRATE FOR SOLUTION FOR
INFUSION
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 Accord is and what it is used for
2.
What you need to know before you are given Zoledronic Acid Accord
3.
How Zoledronic Acid Accord is used
4.
Possible side effects
5.
How to store Zoledronic Acid Accord
6.
Contents of the pack and other information
1.
WHAT ZOLEDRONIC ACID ACCORD IS AND WHAT IT IS USED FOR
The active substance in Zoledronic Acid Accord is zoledronic acid,
which belongs to a group of
substances called bisphosphonates. Zoledronic acid works by attaching
itself to the bone and slowing
down the rate of bone change. It is used:
•
TO PREVENT BONE COMPLICATIONS,
e.g. fractures, in adult patients with bone metastases (spread
of cancer from primary site to the bone).
•
TO REDUCE THE AMOUNT OF CALCIUM
in the blood in adult patients where it is too high due to the
presence of a tumour. Tumours can accelerate normal bone change in
such a way that the
release of calcium from bone is increased. This condition is known as
tumour-induced
hypercalcaemia (TIH).
2.
WHAT YOU NEED TO KNOW BEFORE YOU ARE GIVEN ZOLEDRONIC ACID ACCORD
Follow carefully all instructions given to you by your doctor.
Your doctor will carry out blood tests before you start treatment with
Zoledronic Acid Accord
and will check your response to treatment at regular intervals.
DO NOT RECEIVE ZOLEDRONIC ACID ACCORD:
•
if you are breast-feeding.
•
if you are allergic to zoledronic acid, another bisphosphonate (the
group of substances to
w

Súhrn charakteristických

1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Zoledronic Acid Accord 4 mg/5 ml concentrate for solution for infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
One vial with 5 ml concentrate contains 4 mg zoledronic acid (as
monohydrate)
One ml concentrate contains 0.8 mg zoledronic acid (as monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Concentrate for solution for infusion (sterile concentrate)
Clear and colourless solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
-
Prevention of skeletal related events (pathological fractures, spinal
compression, radiation or
surgery to bone, or tumour-induced hypercalcaemia) in adult patients
with advanced
malignancies involving bone.
-
Treatment of adult patients with tumour-induced hypercalcaemia (TIH).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Zoledronic Acid Accord must only be prescribed and administered to
patients by healthcare
professionals experienced in the administration of intravenous
bisphosphonates. Patients treated with
Zoledronic Acid Accord should be given the package leaflet and the
patient reminder card.
Posology
_ _
_Prevention of skeletal related events in patients with advanced
malignancies involving bone_
_Adults and older people_
The recommended dose in the prevention of skeletal related events in
patients with advanced
malignancies involving bone is 4 mg zoledronic acid every 3 to 4
weeks.
Patients should also be administered an oral calcium supplement of 500
mg and 400 IU vitamin D
daily.
The decision to treat patients with bone metastases for the prevention
of skeletal related events should
consider that the onset of treatment effect is 2-3 months.
_Treatment of TIH_
_Adults and older people_
The recommended dose in hypercalcaemia (albumin-corrected serum
calcium ≥12.0 mg/dl or
3.0 mmol/l) is a single dose of 4 mg zoledronic acid.
_ _
_Renal impairment_
_TIH:_
3
Zoledronic Acid Accord treatment in TIH patients who also have severe
renal impairment should be
cons