Ambroxol hydrochloride
important information for the patient.
This medicine should always be taken exactly as described in this patient leaflet, or according to
the doctor's or pharmacist's instructions.
Envil cough junior contains the active substance – ambroxol hydrochloride, which has expectorant and mucolytic properties in the respiratory tract. The medicine is in the form of a syrup for oral use.
As an adjunct in acute and chronic respiratory diseases with difficulty in expectorating viscous bronchial secretions, such as chronic bronchitis, asthma, bronchiectasis, cystic fibrosis, bronchitis, laryngitis.
If after 4 to 5 days there is no improvement or the patient feels worse, the doctor should be consulted.
Before starting to take Envil cough junior, the doctor or pharmacist should be consulted:
At the beginning of treatment, an excessive amount of fluid secretions from the respiratory tract may appear.
In such a case, coughing should be induced to expectorate it. It may be necessary to aspirate the secretions, then the patient should consult a doctor.
Severe skin reactions associated with the use of ambroxol hydrochloride have been reported. If a rash appears (including changes in the mucous membranes, e.g. mouth, throat, nose, eyes, genitals), the use of Envil cough junior should be discontinued and the doctor should be consulted immediately.
The doctor or pharmacist should be informed about all medicines the patient is currently taking or has recently taken, as well as about medicines the patient plans to take.
The doctor should be informed if the patient is taking:
Envil cough junior should be taken after a meal.
The medicine should not be taken before bedtime.
This subsection does not apply to Envil cough junior, syrup, as this medicine is intended for use in children up to 12 years of age. However, the following information is relevant to the active substance - ambroxol hydrochloride.
If the patient is pregnant or breastfeeding, thinks she may be pregnant, or plans to have a child, she should consult a doctor or pharmacist before taking this medicine.
The use of this medicine is not recommended during pregnancy, as it may be harmful to the fetus.
The use of this medicine is not recommended during breastfeeding, as it passes into breast milk.
The medicine has no influence or negligible influence on the ability to drive and use machines. If headache occurs, the patient should not drive vehicles, operate machinery, or perform other activities that require concentration.
The medicine contains 152.03 mg of propylene glycol in each 5 ml of syrup.
Before administering the medicine to a child under 4 weeks of age, the doctor or pharmacist should be consulted, especially if the child is taking other medicines containing propylene glycol or alcohol.
The medicine contains 10 mg of benzoic acid in each 5 ml of syrup.
Benzoic acid may increase the risk of jaundice (yellowing of the skin and whites of the eyes) in newborns (up to 4 weeks of age).
The medicine contains 2500 mg of sorbitol in each 5 ml of syrup.
Sorbitol is a source of fructose. If the patient (or their child) has previously been diagnosed with intolerance to some sugars or has been diagnosed with hereditary fructose intolerance, a rare genetic disorder in which the patient's body does not break down fructose, the patient should consult a doctor before taking the medicine or giving it to their child.
Sorbitol may cause gastrointestinal discomfort and may have a mild laxative effect.
The medicine contains 0.042 mg of sodium in each 5 ml of syrup.
The medicine contains less than 1 mmol (23 mg) of sodium in 5 ml of syrup, which means the medicine is considered "sodium-free".
This medicine contains 0.02 micrograms of alcohol (ethanol) in 5 ml of syrup. The amount of alcohol in 5 ml of this medicine is equivalent to less than 1 ml of beer or 1 ml of wine.
The small amount of alcohol in this medicine will not cause noticeable effects.
This medicine should always be taken exactly as described in this patient leaflet, or according to the doctor's or pharmacist's instructions. In case of doubt, the doctor or pharmacist should be consulted.
Recommended doses are used to treat acute respiratory diseases and in the initial period of treatment of chronic conditions.
In long-term treatment (more than 14 days), the dose can be reduced to half.
Patient's age | Dose | Administration |
children under 2 years | 2.5 ml of syrup | 2 times a day |
children from 3 to 5 years | 2.5 ml of syrup | 3 times a day |
children from 6 to 12 years | 5 ml of syrup | 2 to 3 times a day |
The medicine should be taken orally.
The medicine should be taken after a meal.
The medicine should not be taken before bedtime.
A measuring cup is attached to the packaging to facilitate dosing, with which the medicine should be measured.
The syrup does not contain sugar.
In case of taking a higher dose of the medicine than recommended, the doctor should be consulted.
Overdose symptoms may occur: nausea, fatigue, excessive secretion of mucus from the bronchi.
The syrup should be taken as soon as possible, and the next dose should be taken at the usual time.
A double dose should not be taken to make up for the missed dose.
In case of any further doubts about the use of this medicine, the doctor or pharmacist should be consulted.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Rarely:may occur in up to 1 in 1,000 people:
Frequency not known:frequency cannot be estimated from the available data
If any side effects occur, including those not listed in this leaflet, the doctor or pharmacist should be informed.
Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
By reporting side effects, more information can be collected on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
Store in a temperature below 25°C. Do not freeze. Store in the original packaging to protect from light.
Do not use this medicine after the expiry date stated on the label and carton.
The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. The pharmacist should be asked how to dispose of medicines that are no longer used. This will help protect the environment.
Envil cough junior is a syrup.
The packaging of the medicine is a brown glass bottle containing 100 ml, 120 ml of syrup, closed with an aluminum cap with a measuring cup, in a cardboard box.
Aflofarm Farmacja Polska Sp. z o.o.
ul. Partyzancka 133/151
95-200 Pabianice
phone: (42) 22-53-100
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