APO-MYCOPHENOLATE mycophenolate mofetil 500 mg tablet bottle

국가: 오스트레일리아

언어: 영어

출처: Department of Health (Therapeutic Goods Administration)

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제품 특성 요약 제품 특성 요약 (SPC)
24-08-2020
공공 평가 보고서 공공 평가 보고서 (PAR)
29-11-2017

유효 성분:

mycophenolate mofetil, Quantity: 500 mg

제공처:

Arrotex Pharmaceuticals Pty Ltd

INN (International Name):

Mycophenolate mofetil

약제 형태:

Tablet

구성:

Excipient Ingredients: microcrystalline cellulose; croscarmellose sodium; colloidal anhydrous silica; magnesium stearate; titanium dioxide; hypromellose; hyprolose; iron oxide red; iron oxide black; macrogol 400

관리 경로:

Oral

패키지 단위:

500 Tablets, 150 Tablets, 50 Tablets

처방전 유형:

(S4) Prescription Only Medicine

치료 징후:

Mycophenolate mofetil is indicated for the prophylaxis of solid organ rejection in adults receiving allogeneic organ transplants.,Mycophenolate mofetil is indicated for the prophylaxis of organ rejection in paediatric patients (2 to 18 years) receiving allogeneic renal transplants.

제품 요약:

Visual Identification: Lavender, film-coated, capsule shaped tablets engraved "APO" on one side and "MYC500" on the other side.; Container Type: Bottle; Container Material: HDPE; Container Life Time: 3 Years; Container Temperature: Store below 25 degrees Celsius

승인 상태:

Registered

승인 날짜:

2011-11-08

제품 특성 요약

                                1
AUSTRALIAN PRODUCT INFORMATION
APO-MYCOPHENOLATE (MYCOPHENOLATE MOFETIL)
TABLETS
1
NAME OF THE MEDICINE
Mycophenolate mofetil
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 500 mg mycophenolate mofetil as the active
ingredient.
For the full list of excipients see section 6.1 LIST OF EXCIPIENTS.
3
PHARMACEUTICAL FORM
500 MG TABLETS:
Lavender coloured, capsule shaped, film coated tablets, engraved with
‘APO’ and ‘MYC500’
on the other.
4
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Mycophenolate mofetil is indicated for the prophylaxis of solid organ
rejection in adults
receiving allogeneic organ transplants.
Mycophenolate mofetil is indicated for the prophylaxis of organ
rejection in paediatric patients
(2 to 18 years) receiving allogeneic renal transplants.
4.2
DOSE AND METHOD OF ADMINISTRATION
APO-Mycophenolate tablets are intended for oral administration.
DOSAGE
The initial dose of mycophenolate mofetil should be given as soon as
clinically feasible
following transplantation. Intravenous administration is recommended
in those patients unable
to take oral medication. However, oral administration should be
initiated as soon as possible.
Note: Alternative preparations will be required for IV administration
and dosages requiring an
oral suspension.
ADULTS
_RENAL TRANSPLANTATION _
The recommended dose in renal transplant patients is 1 g administered
orally or intravenously
twice daily (2 g daily dose).
_CARDIAC TRANSPLANTATION _
The recommended dose in cardiac transplant patients is 1.5 g
administered orally or
intravenously twice daily (3 g daily dose).
2
_HEPATIC TRANSPLANTATION _
The recommended dose in hepatic transplant patients is 1 g
administered intravenously twice
daily (2 g daily dose) followed by 1.5 g administered orally twice
daily (3 g daily dose).
_OTHER TRANSPLANTS _
The recommended dose in other transplants is 2 to 3g per day depending
on the level of
immunosuppression required.
_PAEDIATRICS (2 TO 18 YEARS) _
The recommended dose for renal transplant patients is 600 mg/
                                
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