AT 10

Land: Irland

Sprog: engelsk

Kilde: HPRA (Health Products Regulatory Authority)

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Produktets egenskaber Produktets egenskaber (SPC)
30-05-2014

Aktiv bestanddel:

DIHYDROTACHYSTEROL

Tilgængelig fra:

Intrapharm Laboratories Limited

ATC-kode:

A11CC02

INN (International Name):

DIHYDROTACHYSTEROL

Dosering:

250 Microgram/ML

Lægemiddelform:

Oral Drops Solution

Recept type:

Product subject to prescription which may be renewed (B)

Terapeutisk område:

dihydrotachysterol

Autorisation status:

Not marketed

Autorisation dato:

1986-03-26

Produktets egenskaber

                                PART II
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
AT 10 250 micrograms/ml Oral Drops, Solution
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 1 ml of liquid contains 250 micrograms of dihydrotachysterol in
arachis oil (peanut oil).
For a full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Oral drops, solution
A clear, deep straw- coloured liquid.
4 CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
AT10 is recommended in the treatment of hypocalcaemic tetany due to
hypoparathyroidism.
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
_ADULTS_
In acute cases 3 to 5ml (0.75 to 1.25mg) may be given on each of the
first three days of treatment, followed 2 to 3 days
later by blood and urinary calcium estimations. The maintenance dose
is within the range of 1 to 7ml (0.25 to 1.75mg)
each week, the precise amount depending on the results of serum and
urinary calcium determinations.
In chronic cases, an initial dose of 2ml (0.5mg) daily or on alternate
days, may be sufficient to maintain
normocalcaemia in moderate cases.
AT10 is for oral administration only.
4.3 CONTRAINDICATIONS
Hypersensitivity to dihydrotachysterol and other ingredients of the
preparation.
Hypercalcaemia.
Hypervitaminosis D.
Allergy to nuts (including peanuts).
Do not use with calcium supplements.
4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE
Uncontrolled prolonged administration can result in hypercalcaemia
which may lead to nephrocalcinosis. Accurate
blood calcium determinations must be made at initiation of treatment
and periodically during maintenance. The serum
calcium level should be kept between 2.25-2.5mmol/litre.
Serum phosphate, magnesium and alkaline phosphatase should also be
measured periodically to monitor progress.
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