AEROLET
(ivy leaf extract)




COMPOSITION

100 ml of syrup contains: Active ingredient – ivy leaf extract 0.7 g. Excipients –potassium sorbate, anhydrous citric acid, sorbitol, xanthan gum, black cherry flavoring agent, sunset yellow, purified water.

THERAPEUTIC INDICATIONS

- Symptomatic treatment of acute and chronic respiratory inflammatory diseases accompanied by coughing and production of viscous respiratory tract secretions, difficult to expel, such as acute and chronic bronchitis, especially with bronchial obstruction syndrome.

CONTRAINDICATIONS

- hypersensitivity to any of the component of the medication.

ADVERSE EFFECTS

Allergic reactions (rash, urticaria, Quincke's edema), gastrointestinal disorders (nausea, vomiting, diarrhea).

DOSAGE AND ADMINISTRATION

Aerolet syrup is administered orally after the meals. The syrup is taken undiluted by adults and adolescents, but it is recommended to dilute the syrup with small amount of water if the medicine is taken by infants or children. If other dosage has not been prescribed by doctor, the posology of Aerolet is as follows:

- Infants under 1 year old: 2.5 ml of syrup once daily;

- Children between 1-4 years old: 2.5 ml of syrup 4 times daily;

- Children between 4-10 years old: 2.5 ml of syrup 4 times daily;

- Adults and children aged 10 years and older: 5 ml of syrup 3 times daily.

The duration of treatment depends on the severity of the disease, but the therapy should last for at least 7 days. After the symptoms subside, it is recommended to continue the treatment with Aerolet for 2-3 days. In case of the absence of therapeutic effect or/and the duration of treatment is more than 2 weeks, it is recommended to consult a doctor.

Dose-measuring cup gauged for 5 ml, 10 ml, and 15 ml is used for measuring the dose.

DRUG INTERACTIONS

The antacids containing aluminium ions and ion-exchange resins (cholesteramine), reduce absorption of the medicine.
Hypolipidaemic drugs (especially clofibrate), estrogen, neomicin or progestins increase saturation of bile with cholesterol and can reduce ability of the medicine to dissolve cholesteric bilious concrements.

PREGNANCY AND LACTATION

The administration of Aerolet during pregnancy and lactation is not recommended as there are no sufficient data regarding the safety in this period.

100 ml oral syrup in a light brown glass vial with a protecting screw cap. One vial with a leaflet and a dose-measuring cup in a carton box.

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