Parareg

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

cinacalcet

Available from:

Dompé Biotec S.p.A.

ATC code:

H05BX01

INN (International Name):

cinacalcet

Therapeutic group:

Calcium homeostasis

Therapeutic area:

Hypercalcemia; Parathyroid Neoplasms; Hyperparathyroidism

Therapeutic indications:

Treatment of secondary hyperparathyroidism (HPT) in patients with end-stage renal disease (ESRD) on maintenance dialysis therapy.Mimpara may be used as part of a therapeutic regimen including phosphate binders and/or Vitamin D sterols, as appropriate (see section 5.1).Reduction of hypercalcaemia in patients with:-parathyroid carcinoma.- primary HPT for whom parathyroidectomy would be indicated on the basis of serum calciumlevels (as defined by relevant treatment guidelines), but in whom parathyroidectomy is not clinically appropriate or is contraindicated.

Product summary:

Revision: 6

Authorization status:

Withdrawn

Authorization date:

2004-10-22

Patient Information leaflet

                                B. PACKAGE LEAFLET
57
Medicinal product no longer authorised
PACKAGE LEAFLET : INFORMATION FOR THE USER
PARAREG 30 MG FILM-COATED TABLETS
PARAREG 60 MG FILM-COATED TABLETS
PARAREG 90 MG FILM-COATED TABLETS
Cinacalcet
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE.
Keep this leaflet. You may need to read it again.
If you have further questions, please ask your doctor or pharmacist.
This medicine has been prescribed for you. Do not pass it on to
others. It m
ay harm them, even if their
symptoms are the same as yours.
If any of the side effects gets serious, or if you notice any
side effects not listed in this leaflet, please
tell your doctor or pharmacist.
IN THIS LEAFLET
1.
What Parareg is and what it is used for
2.
Before you take Parareg
3.
How to take Parareg
4.
Possible side effects
5
How to store Parareg
6.
Further information
1.
WHAT PARAREG IS AND WHAT IT IS USED FOR
Parareg works by controlling the levels of parathy
roid hormone (PTH), calcium and phosphorous in
your body. It is used to treat problems with organs called parathyroid
glands. The parathyroids are
four small glands in the neck, near the thyroid gland, that produce
parathyroid hormone (PTH).
Parareg is used:
•
to treat secondary
hyperparathyroidism in patients with kidney disease on dialysis.
•
to reduce high levels of calcium
in the blood (hypercalcaemia) in patients with parathyroid
cancer
•
to reduce high levels of calcium in the blood (hypercalcaemia) in
patients with primary
hyperparathyroidism who still have high calcium levels after removal
of the parathyroid gland
or when removal of the gland is not possible.
In primary and secondary hyperparathyroidism too much PTH is produced
by the parathyroids. This
can cause the loss of calcium in the bones, which can lead to bone
pain and fractures, problems with
blood and heart vessels, kidney stones, mental illness and coma.
2.
BEFORE YOU TAKE PARAREG
DO NOT TAKE PARAREG:
•
DO NOT
take Parareg if y
ou are
ALLERGIC
(hypersensitive) to cinacalcet or any of the oth
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
1
Medicinal product no longer authorised
1.
NAME OF THE MEDICINAL PRODUCT
Parareg 30 mg film-coated tablets.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 30 mg cinacalcet (as hydrochloride).
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
30 mg: Light green, oval, film-coated tablets marked “AMGEN” on
one side and “30” on the other.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Treatment of secondary hyperparathyroidism (HPT) in patients with
end-stage renal disease (ESRD)
on m
aintenance dialysis therapy.
Parareg may be used as part of a therapeutic regim
en including phosphate binders and/or Vitamin D
sterols, as appropriate (see section 5.1).
Reduction of hypercalcaemia in patients with:
•
parathyroid carcinoma.
•
prim
ary HPT for whom parathyroidectomy would be indicated on the basis of
serum calcium
levels (as defined by relevant treatment guidelines), but in whom
parathyroidectomy is not
clinically appropriate or is contraindicated.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
For oral use. It is recommended that Parareg be taken with food or
shortly after a meal, as studies have
shown that bioavailability of cinacalcet is increased when taken with
food (see section 5.2). Tablets
should be taken whole and not divided.
Hepatic impairment
No change in starting dose is necessary. Parareg should be used with
caution in
_ _
patients with m
oderate
to severe hepatic impairment and treatment should be closely monitored
during dose titration and
continued treatment (see sections 4.4 and 5.2).
SECONDARY HYPERPARATHYROIDISM
Adults and elderly (> 65 years)
The recommended starting dose for adults is 30 mg once per day
. Parareg should be titrated every 2 to
4 weeks to a maximum dose of 180 mg once daily to achieve a target
parathyroid hormone (PTH) in
dialysis patients of between 150-300 pg/ml (15.9-31.8 pmol/l) in the
intact PTH (iPTH) assay. PTH
levels should be assessed at least 12 hours
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 14-05-2009
Summary of Product characteristics Summary of Product characteristics Bulgarian 14-05-2009
Public Assessment Report Public Assessment Report Bulgarian 13-05-2009
Patient Information leaflet Patient Information leaflet Spanish 14-05-2009
Public Assessment Report Public Assessment Report Spanish 13-05-2009
Patient Information leaflet Patient Information leaflet Czech 14-05-2009
Public Assessment Report Public Assessment Report Czech 13-05-2009
Patient Information leaflet Patient Information leaflet Danish 14-05-2009
Public Assessment Report Public Assessment Report Danish 13-05-2009
Patient Information leaflet Patient Information leaflet German 14-05-2009
Public Assessment Report Public Assessment Report German 13-05-2009
Patient Information leaflet Patient Information leaflet Estonian 14-05-2009
Public Assessment Report Public Assessment Report Estonian 13-05-2009
Patient Information leaflet Patient Information leaflet Greek 14-05-2009
Public Assessment Report Public Assessment Report Greek 13-05-2009
Patient Information leaflet Patient Information leaflet French 14-05-2009
Public Assessment Report Public Assessment Report French 13-05-2009
Patient Information leaflet Patient Information leaflet Italian 14-05-2009
Public Assessment Report Public Assessment Report Italian 13-05-2009
Patient Information leaflet Patient Information leaflet Latvian 14-05-2009
Public Assessment Report Public Assessment Report Latvian 13-05-2009
Patient Information leaflet Patient Information leaflet Lithuanian 14-05-2009
Summary of Product characteristics Summary of Product characteristics Lithuanian 14-05-2009
Public Assessment Report Public Assessment Report Lithuanian 13-05-2009
Patient Information leaflet Patient Information leaflet Hungarian 14-05-2009
Summary of Product characteristics Summary of Product characteristics Hungarian 14-05-2009
Public Assessment Report Public Assessment Report Hungarian 13-05-2009
Patient Information leaflet Patient Information leaflet Maltese 14-05-2009
Public Assessment Report Public Assessment Report Maltese 13-05-2009
Patient Information leaflet Patient Information leaflet Dutch 14-05-2009
Public Assessment Report Public Assessment Report Dutch 13-05-2009
Patient Information leaflet Patient Information leaflet Polish 14-05-2009
Public Assessment Report Public Assessment Report Polish 13-05-2009
Patient Information leaflet Patient Information leaflet Portuguese 14-05-2009
Summary of Product characteristics Summary of Product characteristics Portuguese 14-05-2009
Public Assessment Report Public Assessment Report Portuguese 13-05-2009
Patient Information leaflet Patient Information leaflet Romanian 14-05-2009
Public Assessment Report Public Assessment Report Romanian 13-05-2009
Patient Information leaflet Patient Information leaflet Slovak 14-05-2009
Public Assessment Report Public Assessment Report Slovak 13-05-2009
Patient Information leaflet Patient Information leaflet Slovenian 14-05-2009
Summary of Product characteristics Summary of Product characteristics Slovenian 14-05-2009
Public Assessment Report Public Assessment Report Slovenian 13-05-2009
Patient Information leaflet Patient Information leaflet Finnish 14-05-2009
Public Assessment Report Public Assessment Report Finnish 13-05-2009
Patient Information leaflet Patient Information leaflet Swedish 14-05-2009
Public Assessment Report Public Assessment Report Swedish 13-05-2009

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