TORVALIPIN 80 atorvastatin (as calcium trihydrate) 80 mg film-coated tablet bottle

Country: Australia

Bahasa: Inggeris

Sumber: Department of Health (Therapeutic Goods Administration)

Beli sekarang

Ciri produk Ciri produk (SPC)
24-08-2020
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
26-11-2017

Bahan aktif:

atorvastatin calcium trihydrate, Quantity: 86.8 mg

Boleh didapati daripada:

Medis Pharma Pty Ltd

INN (Nama Antarabangsa):

atorvastatin calcium trihydrate

Borang farmaseutikal:

Tablet, film coated

Komposisi:

Excipient Ingredients: sodium carbonate; magnesium stearate; glycerol dibehenate; crospovidone; povidone; microcrystalline cellulose; titanium dioxide; hypromellose; macrogol 6000

Laluan pentadbiran:

Oral

Unit dalam pakej:

90, 100

Jenis preskripsi:

(S4) Prescription Only Medicine

Tanda-tanda terapeutik:

Atorvastatin is indicated as an adjunct to diet for the treatment of patients with hypercholesterolaemia. Prior to initiating therapy with atorvastatin, secondary causes of hypercholesterolaemia (e.g. poorly controlled diabetes mellitus, hypothyroidism, nephrotic syndrome, dysproteinaemias, obstructive liver disease, other drug therapy, and alcoholism) should be identified and treated. ,Atorvastatin is indicated in hypertensive patients with multiple risk factors for coronary heart disease (CHD) which may include diabetes, history of stroke or other cerebrovascular disease, peripheral vascular disease or existing asymptomatic CHD (see Clinical Trials, Prevention of Cardiovascular Disease) to reduce the risk of non-fatal myocardial infarction and non-fatal stroke.,These effects do not replace the need to independently control known causes of cardiovascular mortality and morbidity such as hypertension, diabetes and smoking.

Ringkasan produk:

Visual Identification: oval, white, biconvex tablet, embossed with '80' on one side and A on the other side.; Container Type: Bottle; Container Material: HDPE; Container Life Time: 24 Months; Container Temperature: Store below 25 degrees Celsius

Status kebenaran:

Licence status A

Tarikh kebenaran:

2014-10-24

Ciri produk

                                Torvalipin – Product information
Page 1 of 21
AUSTRALIAN PRODUCT INFORMATION – TORVALIPIN (ATORVASTATIN CALCIUM)
1.
NAME OF THE MEDICINE
Atorvastatin Calcium.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
TORVALIPIN tablets come in four strengths and contain 10 mg, 20 mg, 40
mg or 80 mg of
atorvastatin
(calcium).
The
10
mg,
20
mg
and
40
mg
tablets
also
contain:
mannitol,
microcrystalline cellulose, crospovidone, sodium carbonate anhydrous,
povidone, methionine,
magnesium
stearate,
Opadry
White
03F28466
(107577).
The
80
mg
tablets
also
contain
microcrystalline
cellulose,
crospovidone,
sodium
carbonate
anhydrous,
povidone,
glycerol
dibehenate, magnesium stearate and Opadry white 03F28446 (107577). The
tablets are gluten
free.
3.
PHARMACEUTICAL FORM
_TORVALIPIN 10_
Atorvastatin (as calcium) 10 mg; oval, white, biconvex tablet,
embossed with ‘10’ on one side and A on the other side.
_TORVALIPIN 20_
Atorvastatin (as calcium) 20 mg; oval, white, biconvex tablet,
embossed with ‘20’ on one side and A on the other side.
_TORVALIPIN 40_
Atorvastatin (as calcium) 40 mg; oval, white, biconvex tablet,
embossed with ‘40’ on one side and A on the other side.
_TORVALIPIN 80_
Atorvastatin (as calcium) 80 mg; oval, white, biconvex tablet,
embossed with ‘80’ on one side and A on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Atorvastatin
is
indicated
as
an
adjunct
to
diet
for
the
treatment
of
patients
with
hypercholesterolaemia.
Prior to initiating therapy with atorvastatin, secondary causes of
hypercholesterolaemia (e.g.
poorly controlled diabetes mellitus, hypothyroidism, nephrotic
syndrome, dysproteinaemias,
obstructive liver disease, other drug therapy and alcoholism) should
be identified and treated.
Hypertensive patients with multiple risk factors for CHD which may
include diabetes, history of
stroke or other cerebrovascular disease, peripheral vascular disease
or existing asymptomatic CHD
(see Section 5.1 PHARMACODYNAMIC PROPERTIES, CLINICAL TRIALS,
PREVENTION OF CARDIOVASCULAR
DISEASE)
                                
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