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  • Percutaféine Gel 5% 192g

Percutaféine Gel 5% 192g


€8.99

Indications: Symptomatic treatment of localized subcutaneous fatty deposits.

48 hours
Qty
In stock

In this manual :

1. WHAT IS PERCUTAFEINE, gel AND WHAT IS IT USED FOR?

2. WHAT DO YOU NEED TO KNOW BEFORE USING PERCUTAFEINE, gel?

3. HOW DO I USE PERCUTAFEINE, gel?

4. WHAT ARE THE POSSIBLE SIDE EFFECTS?

5. HOW TO USE PERCUTAFEINE, gel?

6. ADDITIONAL INFORMATION

1. WHAT IS PERCUTAFEINE, gel AND WHAT IS IT USED FOR?

Pharmacotherapeutic class

Not applicable.

Therapeutic indications

Symptomatic treatment of localized subcutaneous fat deposits.

2. WHAT YOU SHOULD KNOW BEFORE USING PERCUTAFEINE, gel

List of information needed before taking the medicine

Not applicable.

Contraindications

Never use PERCUTAFEINE, gel in the following case:

- If you are allergic (hypersensitive) to caffeine or any of the other components contained in PERCUTAFEINE, gel.

IN CASE OF DOUBT, IT IS ESSENTIAL TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE

Precautions for use; special warnings

Be careful with PERCUTAFEINE, gel:

- do not apply to irritated or injured skin,

- because of the alcohol content of the gel, it should not be used in patients treated with disulfiram (ESPERAL),

- this treatment does not constitute in any way a basic treatment for obesity.

IF IN DOUBT, DO NOT HESITATE TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.

Interactions with other medicines

Taking or using other medicines

IN ORDER TO AVOID POSSIBLE INTERACTIONS WITH OTHER MEDICINES, YOU SHOULD ALWAYS INFORM YOUR DOCTOR OR PHARMACIST OF ANY OTHER TREATMENT IN PROGRESS

Interactions with food and drink

Not applicable.

Interactions with herbal products or alternative therapies

Not applicable.

Use during pregnancy and lactation

Pregnancy and lactation

This medicine should be used with caution during pregnancy and lactation. In the case of breastfeeding women, if applied to the breasts, clean the skin before each feed following application to the breasts.

In general, it is advisable to ask your doctor or pharmacist for advice before taking any medication.

Sportsmen

Not applicable.

Effects on ability to drive or use machines

Not applicable.

List of excipients with a known effect

Not applicable.

3. HOW TO USE PERCUTAFEINE, gel

Instructions for proper use

Not applicable.

Dosage, Method and/or route(s) of administration, Frequency of administration and Duration of treatment

Dosage

Apply locally 10 to 20 g per day and massage in.

Symptoms and instructions in case of overdose

Not applicable.

Instructions in case of missed dose(s)

Not applicable.

Risk of withdrawal syndrome

Not applicable.

4. WHAT ARE THE POSSIBLE SIDE EFFECTS?

Description of side effects

Like all medicines, PERCUTAFEINE, gel is likely to have undesirable effects, although not everyone is subject to them.

Redness of the skin may appear, in which case it is advisable to stop treatment.

If you notice any side effects not mentioned in this leaflet, or if any side effects become serious, please tell your doctor or pharmacist.

5. HOW TO CONSERVE PERCUTAFEINE, gel?

Keep out of the reach and sight of children.

Expiry date

Do not use PERCUTAFEINE, gel after the expiry date stated on the outer packaging.

Storage conditions

Do not refrigerate.

If necessary, warnings against certain visible signs of deterioration

Medicines should not be disposed of down the drain or in the household waste. Ask your pharmacist what to do with unused medicines. This will help to protect the environment.

6. ADDITIONAL INFORMATION

Complete list of active substances and excipients

What does PERCUTAFEINE gel contain?

The active substance is:

Caffeine ............................................................................................................................................ 5,000 g

Per 100 g of gel.

The other components are:

Carbomer (synthalene K), trolamine, cocoate of macrogol 7 glycerol (CETHIOL HE), 96 per cent ethanol, purified water.

Pharmaceutical form and content

What is PERCUTAFEINE gel and what does it contain?

This medicine is available as a gel in tubes of 20 g, 72 g, 80 g, 96 g, 144 g, 150 g, 192 g.

Name and address of the marketing authorisation holder and of the manufacturing authorisation holder responsible for batch release, if different

Holder

PIERRE FABRE MEDICAMENT

45, PLACE ABEL GANCE

92100 BOULOGNE BILLANCOURT

Operator

LABORATOIRES PIERRE FABRE MEDICAMENT

45, PLACE ABEL GANCE

92100 BOULOGNE

Manufacturer

Not known

Names of the medicinal product in the Member States of the European Economic Area

Not applicable.

Date of approval of the notice

The last date on which this leaflet was approved was {date}.

MA under exceptional circumstances

Not applicable.

Internet information

Detailed information on this medicinal product is available on the website of Afssaps (France).

Information reserved for health professionals

Not applicable.

Other

Not applicable.

3400934628825

Specific References

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