Tadalafil Alphapharm tadalafil 5mg film-coated tablets blister pack

국가: 오스트레일리아

언어: 영어

출처: Department of Health (Therapeutic Goods Administration)

지금 구매하세요

환자 정보 전단 환자 정보 전단 (PIL)
26-05-2021
제품 특성 요약 제품 특성 요약 (SPC)
24-05-2021
공공 평가 보고서 공공 평가 보고서 (PAR)
16-04-2021

유효 성분:

tadalafil, Quantity: 5 mg

제공처:

Alphapharm Pty Ltd

약제 형태:

Tablet, film coated

구성:

Excipient Ingredients: croscarmellose sodium; povidone; microcrystalline cellulose; sodium lauryl sulfate; poloxamer; colloidal anhydrous silica; lactose; magnesium stearate; titanium dioxide; lactose monohydrate; hypromellose; triacetin; iron oxide yellow

관리 경로:

Oral

패키지 단위:

28, 7

처방전 유형:

(S4) Prescription Only Medicine

치료 징후:

Tadalafil Alphapharm is indicated for the treatment of:,? erectile dysfunction (ED) in adult males,? moderate to severe lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH) in adult males

제품 요약:

Visual Identification: A light yellow, film-coated, round, biconvex tablet debossed with M on one side of the tablet and TL over 2 on the other side; Container Type: Blister Pack; Container Material: PVC/PE/PVDC/Al; Container Life Time: 36 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Child resistant closure

승인 상태:

Registered

승인 날짜:

2021-02-03

환자 정보 전단

                                TADALAFIL ALPHAPHARM
T
A
D
A
L
A
F
I
L
A
L
P
H
A
P
H
A
R
M
CONSUMER MEDICINE INFORMATION (CMI) SUMMARY
The full CMI on the next page has more details. If you are worried
about using this medicine, speak to your doctor or pharmacist.
1.
WHY AM I USING TADALAFIL ALPHAPHARM?
TADALAFIL ALPHAPHARM contains the active ingredient tadalafil.
TADALAFIL ALPHAPHARM is used to treat erectile dysfunction
and urinary symptoms associated with benign prostatic hyperplasia in
adult men.
For more information, see Section 1. Why am I using TADALAFIL
ALPHAPHARM? in the full CMI.
2.
WHAT SHOULD I KNOW BEFORE I USE TADALAFIL ALPHAPHARM?
Do not use if you have ever had an allergic reaction to TADALAFIL
ALPHAPHARM or any of the ingredients listed at the end of the
CMI.
Do not take TADALAFIL ALPHAPHARM if you are currently taking any
nitrates or amyl nitrite.
TALK TO YOUR DOCTOR IF YOU HAVE ANY OTHER MEDICAL CONDITIONS SUCH AS
HEART PROBLEMS OR IF YOU TAKE ANY OTHER MEDICINES.
For more information, see Section 2. What should I know before I use
TADALAFIL ALPHAPHARM? in the full CMI.
3.
WHAT IF I AM TAKING OTHER MEDICINES?
Some medicines may interfere with TADALAFIL ALPHAPHARM and affect how
it works.
A list of these medicines is in Section 3. What if I am taking other
medicines? in the full CMI.
4.
HOW DO I USE TADALAFIL ALPHAPHARM?
•
Always take TADALAFIL ALPHAPHARM exactly as your doctor has told you.
•
Follow all directions given to you by your doctor or pharmacist.
More instructions can be found in Section 4. How do I use TADALAFIL
ALPHAPHARM? in the full CMI.
5.
WHAT SHOULD I KNOW WHILE USING TADALAFIL ALPHAPHARM?
THINGS YOU
SHOULD DO
•
Remind any doctor, dentist or pharmacist that you are using TADALAFIL
ALPHAPHARM.
•
If you have emergency treatment for any suspected heart condition,
tell the emergency medical or
ambulance staff that you are taking TADALAFIL ALPHAPHARM.
THINGS YOU
SHOULD NOT DO
•
Do not take TADALAFIL ALPHAPHARM to treat any other complaints.
•
Do not give your medicine to anyone else, even if they have
                                
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제품 특성 요약

                                AUSTRALIAN PRODUCT INFORMATION
TADALAFIL ALPHAPHARM
_Tadalafil film coated tablets _
1
NAME OF THE MEDICINE
Tadalafil
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each TADALAFIL ALPHAPHARM film-coated tablet contains 2.5 mg, 5 mg, 10
mg or 20 mg of tadalafil
as the active ingredient.
Excipients of known effect: Sugars (as lactose).
For the full list of excipients, see section 6.1 List of Excipients.
3
PHARMACEUTICAL FORM
2.5mg: a light yellow, film-coated, round, biconvex tablet debossed
with ‘M’ on one side of the tablet and ‘TL
over 1’ on the other side.
5 mg: a light yellow, film-coated, round, biconvex tablet debossed
with ‘M’ on one side of the tablet and ‘TL
over 2’ on the other side.
10 mg: a light yellow, film-coated, round, biconvex tablet debossed
with ‘M’ on one side of the tablet and
‘TL3’ on the other side.
20 mg: a light yellow, film-coated, round, biconvex tablet debossed
with ‘M’ on one side of the tablet and
‘TL4’ on the other side.
4
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
TADALAFIL ALPHAPHARM is indicated for the treatment of:
•
erectile dysfunction (ED) in adult males
•
moderate to severe lower urinary tract symptoms (LUTS) associated with
benign prostatic hyperplasia
(BPH) in adult males
4.2
DOSE AND METHOD OF ADMINISTRATION
TADALAFIL ALPHAPHARM is for oral use.
TADALAFIL ALPHAPHARM can be taken with or without food.
ERECTILE DYSFUNCTION IN ADULT MALES - ON-DEMAND DOSING
The recommended dose of TADALAFIL ALPHAPHARM is either 10 mg or 20 mg,
taken prior to anticipated
sexual activity. The maximum recommended dose is 20 mg. The maximum
recommended dosing frequency
is once per day. TADALAFIL ALPHAPHARM 10 and 20 mg is intended for use
prior to anticipated sexual
activity and is not for continuous daily use.
Tadalafil has been proven effective up to 36 hours after dosing and,
in some patients, as early as 16 minutes
after dosing. Patients may initiate sexual activity at varying time
points relative to dosing in order to determine
their own optimal window
                                
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