Acetamol early childhood 100 mg/ ml - antipyretic analgesic drops - 30 ml

Product Description

Symptomatic treatment of fever and mild to moderate pain.

Composition

ACETAMOL early childhood 100 mg/mL oral drops; 30 ml of oral drops contain:

Active ingredient: paracetamol 3 g One drop contains: Active ingredient: paracetamol 2.8 mg. 

Excipients: 

ACETAMOL early childhood 100 mg / mL oral drops, solution: Macrogol 300, glycerol, diethylene glycol monoethyl ether, sorbitol, sodium saccharin, propyl gallate, orange flavoring, lemon flavoring, purified water. 

Contraindications

Hypersensitivity to the active ingredient, to any of the excipients or other closely related substances from a chemical point of view, in particular to other analgesics and antipyretics.

Dosage

ACETAMOL early childhood 100 mg/mL oral drops solutioncan be taken by children of any age by calculating the correct dose based on weight. However, the medicine is identified as Early Childhood because, being packaged in 30 mL bottles, it can be taken by children of any age. may be insufficient for children weighing more than 15 kg and cannot cover an adequate number of days of treatment.

Warnings and Precautions

Children Consult your doctor before administering the medicine to a child.

Warnings relating to excipients

Oral drops: Patients with rare hereditary problems of fructose intolerance should not take this medicine. Any browning of the solution does not affect the efficacy and tolerability of the product in any way. Effervescent granules, syrup: Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption, or sucrase-isomaltase insufficiency should not take this medicine. The product contains sugar: of which there are no known side effects. should be taken into account when administering to diabetics or those on low-calorie diets.

Side Effects

Skin reactions of various types and severity have been reported with the use of paracetamol, including cases of erythema multiforme, Stevens-Johnson syndrome, and epidermal necrolysis. Hypersensitivity reactions such as angioedema, laryngeal edema, and anaphylactic shock have been reported. The following side effects have also been reported: thrombocytopenia, leukopenia, anemia, agranulocytosis, alterations in liver function and hepatitis, alterations affecting the kidney (acute renal failure, interstitial nephritis, hematuria, anuria), gastrointestinal reactions, and dizziness. Reporting of suspected adverse reactions Reporting suspected adverse reactions that occur after authorization of the medicinal product is important, as it allows continuous monitoring of the benefit/risk balance of the medicinal product.

Pregnancy and Breastfeeding

Although clinical studies in pregnant or breastfeeding patients have not revealed any particular contraindications to the use of paracetamol, nor have it caused any adverse effects on the mother or child, it is recommended to administer the product only in cases of real need and under the direct supervision of a doctor.

Storage

This medicinal product does not require any special storage conditions.