FERVEX / Fervex for children with raspberry flavor x 8 sachets
COMPOSITION
Paracetamol (Paracetamol) 0.280 g Pheniramine maleate (Phemramine maleate) 0.010 g
Vitamin C (Ascorbic acid) 0.100 g
Excipients: sucrose, riboflavin phosphate (sodium salt), anhydrous magnesium nitrate, aspartame, banana-caramel flavor sq for one sachet
MEDICINAL FORM
Granules for oral solution
CASES IN WHICH THIS MEDICATION SHOULD BE USED
This medicine contains paracetamol (pain reliever and fever reducer), pheniramine (anti-allergy) and vitamin C. It is used for the short-term treatment of fever and nasal discharge in acute nasopharyngitis in children.
IMPORTANT!
- CASES IN WHICH THIS MEDICATION SHOULD NOT BE USED
This medicine SHOULD NEVER BE USED in the following cases:
• allergy to any of the ingredients
• serious liver disease
• some forms of glaucoma
• diseases of the prostate and urinary tract
• in children under 6 years old
• in cases of phenylketonuria (a hereditary disease detected at birth) due to the presence of aspartame
• with fructose intolerance, glucose-galactose malabsorption syndrome or sucrose-isomaltase deficiency due to the presence of glucose.
WHEN IN DOUBT ALWAYS CONSULT YOUR DOCTOR OR PHARMACIST
■ SPECIAL WARNINGS
Consult a doctor immediately in case of overdose or accidentally taking too high a dose.
This medicine contains paracetamol. Other medicines also contain this substance. Do not combine such drugs so as not to exceed the recommended daily dose (see "Dosage").___
Do not exceed the indicated dosage and consult a doctor immediately in case of accidental overdose.
The temperature should drop quickly. Consult a doctor immediately if the temperature does not go down or worsens, or if other disorders appear.
Inform the doctor if the illness lasts more than 3 days.
Do not combine with other drugs (especially sedatives) without first consulting your doctor or pharmacist
Inform your doctor in case of kidney disease
WHEN IN DOUBT, DON'T HESITATE TO CALL YOUR DOCTOR OR PHARMACIST.
■ Keep out of reach of children.
■ Each sachet contains 2.4 g of sucrose, which should be taken into account in low-sugar diets or diabetes.
■ DRUG AND OTHER INTERACTIONS
TO AVOID POTENTIAL DRUG INTERACTIONS, YOU SHOULD ALWAYS INFORM YOUR DOCTOR OR PHARMACIST THAT YOU ARE TAKING OTHER MEDICINES.
To avoid the harmful effects of an overdose, DO NOT COMBINE other medicines containing antihistamines or paracetamol WITHOUT CONSULTING A PHYSICIAN.
• PRECAUTIONS FOR USE
WHEN IN DOUBT, DON'T HESITATE TO CALL YOUR DOCTOR OR PHARMACIST.
Alcohol should not be taken during treatment.
• PREGNANCY AND BREAST-FEEDING
As a precaution, this drug is not recommended during pregnancy and breastfeeding.
AS A GENERAL RULE, ALWAYS CONSULT YOUR DOCTOR OR PHARMACIST BEFORE TAKING ANY MEDICATION WHILE PREGNANT OR BREASTFEEDING.
• EFFECT ON ABILITY TO DRIVE OR OPERATE MACHINERY
People who drive motor vehicles and operate machinery are warned about the risk of drowsiness when using this medicine.
This effect is enhanced by taking alcohol or drugs containing alcohol.
• LIST OF EXCIPIENTS THAT SHOULD BE CONSIDERED FOR SAFE USE IN CERTAIN PATIENTS
Sucrose
Aspartame (source of phenylalanine) (E951)
HOW TO TAKE THIS MEDICINE
• DOSAGE
■ children from 6 to 10 years: 1 sachet 2 times in 24 hours
■ children from 10 to 12 years: 1 sachet 3 times in 24 hours
■ children from 12 to 15 years: 1 sachet 4 times in 24 hours
METHOD AND METHOD OF ADMINISTRATION
An interval of at least 4 hours is required between applications. Sachets should be taken with a sufficient amount of hot or cold water. Oral administration.
• TREATMENT FREQUENCY
In cases of acute renal failure (creatinine clearance < 10 ml/mm), the interval between two doses should be at least 8 hours. The maximum dose of paracetamol is 80 mg/kg/day in children weighing less than 37 kg and 3 g per day in children weighing 3 8 to 50 kg.
Each sachet contains 2.4 g of sugar.
MEDICAL INSTRUCTIONS MUST BE STRICTLY FOLLOWED AT ALL TIMES.
• DURATION OF TREATMENT
Do not use this medicine for long-term treatment without medical advice, especially if the disturbances last more than 3 days
• OVERDOSE BEHAVIOR
In case of accidental overdose, inform your doctor or pharmacist.
ADVERSE DRUG REACTIONS
AS WITH ALL ACTIVE PRODUCTS, THIS MEDICATION MAY CAUSE ADVERSE REACTIONS OF GREATER OR LESS SEVERITY IN CERTAIN INDIVIDUALS:
Occurrence of an acute attack of glaucoma in people who have such a predisposition.
■ Urinary disorders (significant decrease in urine, difficulty urinating)
■ Dry mouth, accommodation disorders (the ability of the eye to adjust to see at different distances), constipation
■ Impaired memory or concentration, confusion, dizziness (more common in elderly patients).
■ Lack of coordination in movements, tremors.
■ Drowsiness, reduced attention - more pronounced at the beginning of treatment.
■ Rare cases of skin rash, reddening of the skin, or an allergic reaction in the form of sudden swelling of the face or neck or sudden malaise with a drop in blood pressure have been reported. Treatment should be stopped immediately, a doctor should be consulted and no more medicines containing paracetamol or pheniramine should be taken.
■ A few rare cases of changes in laboratory test results have been reported, e.g. very low levels of some white blood cells or platelets, which can cause nosebleeds or bleeding gums. In this case, consult a doctor
NOTIFY YOUR DOCTOR OR PHARMACIST OF ANY ADVERSE DRUG REACTIONS 3 A NOT MENTIONED IN THIS INFORMATION.
STORAGE
* Do not use after the expiration date indicated on the package.
- SPECIAL STORAGE PRECAUTIONS
This medicinal product does not require special storage conditions.
Keep out of the reach of children
