
Go-on ONE 1 INTRA JOINT INJECTION 6ML GOON
Indicated in the symptomatic treatment of osteoarthritis.
IMPORTANT! New orders to the United States are temporarily suspended.
Indications: This medicine is indicated for the treatment of colds, rhinitis, rhinopharyngitis and influenza in adults (15 years and older): clear nasal discharge and watery eyes, sneezing, headache and/or fever.
In this manual :
1. WHAT IS FERVEX SUGAR-FREE, granulated drinkable solution in sachet AND WHAT IS IT USED FOR?
2. WHAT YOU SHOULD KNOW BEFORE TAKING FERVEX SUGAR-FREE, granulated for drinkable solution in sachet?
3. HOW DO I TAKE FERVEX SUGAR-FREE, granules for drinkable solution in sachet?
4. WHAT ARE THE POSSIBLE SIDE EFFECTS?
5. HOW TO USE FERVEX SUGAR-FREE, granules for drinkable solution in sachet?
6. ADDITIONAL INFORMATION
1. WHAT IS FERVEX SUGAR-FREE, granulated oral solution in sachet AND WHAT IS IT USED FOR?
This medicine is indicated for the treatment of colds, rhinitis, rhinopharyngitis and influenza in adults (15 years and older):
- of clear nasal discharge and watery eyes,
- sneezing,
- headaches and/or fever.
2. WHAT YOU SHOULD KNOW BEFORE TAKING FERVEX SUGAR-FREE, granules for drinkable solution in sachet
Not applicable.
Do not take FERVEX SUGAR-FREE, granulated drinkable solution in sachet in the following cases:
- children under 15 years of age,
- in case of previous allergy to the constituents of the product,
- in case of certain forms of glaucoma (increased pressure in the eye),
- in case of difficulties in urinating of prostatic or other origin,
- in case of severe liver disease due to the presence of paracetamol,
- in case of phenylketonuria (hereditary disease detected at birth), due to the presence of aspartam.
You should not generally use this medicine, unless your doctor advises otherwise, during pregnancy and breast-feeding.
IF IN DOUBT, IT IS ESSENTIAL TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE.
Be careful with FERVEX SUGAR-FREE, granulated solution for drinking in sachet:
Special warnings
DO NOT LEAVE THIS MEDICINE WITHIN THE REACH OF CHILDREN
- it is imperative that the dosage, the 5-day treatment period and the contraindications are strictly observed.
- It is not advisable to drink alcoholic beverages, take medicines containing alcohol or sedatives during treatment.
In case of overdose or if you have taken too much by mistake, consult your doctor immediately. This medicine contains paracetamol and pheniramine. Other medicines contain them. Do not combine them, so that you do not exceed the recommended daily dose (see "Dosage" section). |
Tell your pharmacist or doctor if you are taking any other medicine during the same period.
If you have:
- severe liver or kidney disease,
- predisposition to constipation, dizziness and urinary disorders,
this medicine should only be used after consulting your doctor.
Precautions for use
In case of: purulent nasal discharge, persistent fever, lack of improvement after 5 days of treatment, CONSULT YOUR DOCTOR.
To avoid the adverse effects of an overdose, DO NOT COMBINE without MEDICAL ADVICE other drugs containing antihistamines or paracetamol. IF IN DOUBT, DO NOT HESITATE TO ASK YOUR DOCTOR OR PHARMACIST FOR ADVICE. |
This medicine may cause drowsiness increased by alcohol: it is preferable to start the treatment in the evening and to abstain from alcoholic beverages during the treatment.
Not applicable.
Not applicable.
Pregnancy and breastfeeding
Ask your doctor or pharmacist for advice before taking any medicine. |
Pregnancy
This medicine should not be taken during pregnancy.
Breastfeeding
This medicine should not be taken during breastfeeding.
Not applicable.
Driving and use of machines
Attention is drawn, particularly in drivers of vehicles and users of machines, to the possibility of drowsiness or reduced vigilance associated with the use of this medicine.
This phenomenon is accentuated by the use of alcoholic beverages, medicines containing alcohol or sedative medicines.
List of excipients with a notorious effect:
Aspartam (source of phenylalanine) (E 951).
3. HOW TO TAKE FERVEX SUGAR-FREE, granulated oral solution in sachet?
Not applicable.
Dosage, Method and/or route(s) of administration, Frequency of administration and Duration of treatment
For adults only (from 15 years of age)
1 sachet to be repeated if necessary after at least 4 hours, without exceeding 3 sachets per day.
Mode and route of administration
Oral use.
The sachets should be taken in a sufficient quantity of water, cold or hot.
During flu-like conditions it is better to take this medicine in warm water in the evening.
Frequency of administration
In case of renal insufficiency (creatinine clearance less than 10 ml/min), the interval between two doses should be at least 8 hours.
Duration of treatment
The maximum duration of treatment is 5 days.
If you have taken more FERVEX SUGAR-FREE granules in a sachet than you should have: STOP THE TREATMENT AND SEEK MEDICAL CARE IMMEDIATELY.
If you forget to take FERVEX SUGAR-FREE granules in a sachet: DO NOT TAKE A DOUBLE DOSE TO MAKE UP FOR THE SINGLE DOSE YOU MISSED.
Not applicable.
4. WHAT ARE THE POSSIBLE SIDE EFFECTS?
Like all medicines, FERVEX SUGAR-FREE, granules for oral solution in sachet is likely to have undesirable effects, although not everyone is subject to them.
- The onset of acute glaucoma in susceptible individuals.
- Urinary disorders (significant decrease in urination, difficulty in urinating).
- Dry mouth, visual disturbances, constipation.
- Memory or concentration problems, confusion, dizziness (more frequent in the elderly).
- Motor incoordination, tremors.
- Drowsiness, decreased alertness, more pronounced at the beginning of treatment.
- A drop in blood pressure when moving to a standing position, which may be accompanied by dizziness.
- In rare cases, a rash or redness of the skin or an allergic reaction may occur, which may include sudden swelling of the face and neck or sudden discomfort with a fall in blood pressure. Treatment must be stopped immediately, your doctor must be informed and you must not take any other medication containing paracetamol or pheniramine.
- In exceptional cases, biological changes requiring a blood test have been observed: abnormally low levels of certain white blood cells or certain blood cells such as platelets, which may result in nose or gum bleeds. In this case, consult a doctor.
If you notice any side effects not listed in this leaflet, or if any side effects become serious, please tell your doctor or pharmacist.
5. HOW TO USE FERVEX SUGAR-FREE, granulated solution for drinking in sachet?
Keep out of the reach and sight of children.
Do not use FERVEX SUGAR-FREE, granules for oral solution in sachet after the expiry date stated on the box.
Store away from heat and moisture.
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.
What does FERVEX SUGAR-FREE, granulated oral solution in sachet, contain and what is in the outer packaging?
The active ingredients are:
Paracetamol .................................................................................................................................... 0,500 g
Ascorbic acid ............................................................................................................................. 0,200 g
Pheniramine maleate .................................................................................................................... 0,025 g
For a sachet of 4.950 g.
Other components are:
Mannitol, anhydrous citric acid, polyvidone, anhydrous magnesium citrate, aspartam, West Indian flavour 87 57 48 (essential oils of lemon, cinnamon and clove, natural extracts of rum and vanilla, balsam of Peru, caramel, on a carrier composed of maltodextrin cerelose and gum arabic).
What is FERVEX SUGAR-FREE, granulated drinkable solution in a sachet and what does it contain?
This medicine comes in the form of granules for oral solution in sachets.
Boxes of 6, 8, 10 and 12 sachets.
Name and address of the marketing authorisation holder and of the manufacturing authorisation holder responsible for batch release, if different
UPSA CONSEIL
3, rue Joseph Monier
92500 RUEIL-MALMAISON
UPSA CONSEIL
3, rue Joseph Monier
BP 325
92506 RUEIL-MALMAISON CEDEX
BRISTOL-MYERS SQUIBB
304, avenue du Docteur Jean Bru
47000 AGEN
or
BRISTOL-MYERS SQUIBB
979, avenue des Pyrenees
47520 LE PASSAGE
Not applicable.
The last date on which this package insert was approved was {date}.
Not applicable.
Detailed information on this medicinal product is available on the website of Afssaps (France).
Not applicable.
Not applicable.
Indicated in the symptomatic treatment of osteoarthritis.
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