Australian By Nature Propolis Mouth Spray

Country: Awstralja

Lingwa: Ingliż

Sors: Department of Health (Therapeutic Goods Administration)

Ingredjent attiv:

Propolis resin, Quantity: 100 mg/mL (Equivalent: Propolis, Qty 200 mg/mL; Equivalent: lead, Qty 100 ng/mL)

Disponibbli minn:

Australian By Nature Pty Ltd

INN (Isem Internazzjonali):

Propolis

Għamla farmaċewtika:

Liquid, multipurpose

Kompożizzjoni:

Excipient Ingredients: Spearmint oil; Eucalyptus Oil; propylene glycol

Rotta amministrattiva:

Oral

Klassi:

Medicine Listed

Indikazzjonijiet terapewtiċi:

Antioxidant/Reduce free radicals formed in the body ; Helps reduce/decrease free radical damage to body cells ; Maintain/support general health and wellbeing ; Traditionally used in Naturopathic medicine to Soothe/relieve mouth/oral irritation ; Traditionally used in Naturopathic medicine to Decrease/reduce/relieve symptoms of mild mouth ulcers ; Maintain/support immune system health ; Maintain/support healthy immune system function

Sommarju tal-prodott:

Visual Identification: ;

L-istatus ta 'awtorizzazzjoni:

Listed

Data ta 'l-awtorizzazzjoni:

2006-07-04

Fuljett ta 'informazzjoni

DUROMINE
®
D
u
r
o
m
i
n
e
®
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 DUROMINE?
Duromine contains the active ingredient phentermine. Duromine is used
to reduce body weight in obese or overweight patients. For
more information, see Section 1. Why am I using Duromine? in the full
CMI.
2.
WHAT SHOULD I KNOW BEFORE I USE DUROMINE?
Do not use if you have ever had an allergic reaction to phentermine or
any of the ingredients listed at the end of the CMI.
There are a number of circumstances in which a person should not use
this medicine or may need to use caution. It is important to
understand if these apply to you before taking Duromine (see the full
CMI for more details).
TALK TO YOUR DOCTOR IF YOU HAVE ANY OTHER MEDICAL CONDITIONS, TAKE ANY
OTHER MEDICINES, OR ARE PREGNANT OR PLAN TO BECOME
PREGNANT OR ARE BREASTFEEDING.
For more information, see Section 2. What should I know before I use
Duromine? in the full CMI.
3.
WHAT IF I AM TAKING OTHER MEDICINES?
Some medicines may interfere with Duromine 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 DUROMINE?
•
Carefully follow all directions given by your doctor or other
healthcare professionals and never change the dose yourself.
•
The usual dose of Duromine is one capsule a day.
•
Swallow the capsule whole with plenty of water. Do not chew or open
the capsules.
More instructions can be found in Section 4. How do I use Duromine? in
the full CMI.
5.
WHAT SHOULD I KNOW WHILE USING DUROMINE?
THINGS YOU
SHOULD DO
•
Remind any doctor, dentist, or pharmacist you visit that you are using
Duromine.
•
If you are going to have surgery, tell the surgeon or anaesthetist
that you are taking Duromine.
•
Stop taking and contact your doctor immediately if you become pregnant
while taking Duromine.
•
Tell your doctor immediately if you

Karatteristiċi tal-prodott

1
AUSTRALIAN PRODUCT INFORMATION – DUROMINE (PHENTERMINE)
CAPSULE
1
NAME OF THE MEDICINE
Phentermine
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each Duromine capsule contains phentermine as an ion-exchange resin
complex equivalent to 15,
30 or 40 mg phentermine depending on strength. The ion-exchange resin
is quite stable, highly
insoluble and without pharmacological effect until it reacts with
cations (hydrogen, potassium,
sodium etc) present in the gastrointestinal fluids. Phentermine is
then released from the resin
complex at a rate dependent on the total concentration of these
cations. Since this concentration
is fairly constant throughout the entire gastrointestinal tract,
continuous and controlled ionic
release occurs over a 10 to 14 hour period.
Each Duromine capsule also contains, as inactive ingredients, lactose
monohydrate, liquid
paraffin, magnesium stearate, gelatin capsules hard PI (1947),
titanium dioxide, iron oxide black
(CI 77499) and sodium polystyrene sulfonate. In addition, Duromine 15
also contains brilliant
blue FCF (CI 42090), iron oxide yellow (CI 77492); Duromine 30 also
contains iron oxide red (CI
77491); Duromine 40 also contains erythrosine (CI 45430) and sunset
yellow FCF (CI 15985).
Duromine capsules are gluten-free.
Excipient with known effect:
Each modified-release capsule contains sugars as lactose monohydrate.
3
PHARMACEUTICAL FORM
Modified-release capsule.
15mg capsule – grey and green, marked Duromine 15 on cap and body
30mg capsule – grey and reddish brown, marked Duromine 30 on cap and
body
40mg capsule – grey and orange, marked Duromine 40 on cap and body
4
CLINICAL PARTICULARS
4.1
T
HERAPEUTIC INDICATIONS
Duromine is an anorectic agent indicated in the management of obesity
as a short-term adjunct
in a medically monitored comprehensive regimen of weight reduction
based, for example, on
exercise, diet (caloric/kilojoule restriction) and behaviour
modification in obese patients with a
body mass index (BMI) of 30 kg/m
2
or greater. The treatment with Duromine can be in