Teva Pharmaceutical Industries Ltd,Ambrosol syrup 30mg/5ml 200ml,Ambrosol syrop 30mg/5ml 200ml

Compound
The active ingredient is ambroxol hydrochloride. 5 ml of syrup (1 scoop) contains 30 mg of ambroxol hydrochloride. – Other ingredients of the drug: liquid sorbitol 70% (E420), glycerin (E422), citric acid monohydrate (E330), propylene glycol (E1520), methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate (E216), raspberry flavor, purified water.
Indications
Ambrosol Teva is indicated for acute and chronic respiratory diseases that cause difficulty in expectorating viscous bronchial secretions, such as:
acute and chronic bronchitis,
bronchial asthma,
cystic fibrosis,
emphysema,
bronchiectasis.
Action
Teva Ambrosol syrup contains the active substance ambroxol hydrochloride. Increases the amount of mucus in the respiratory tract, reduces its viscosity, accelerates the transport of secretions into the respiratory tract, which facilitates expectoration and relieves coughing.
Dosage:
Always take Ambrosol Teva exactly as your doctor prescribed. If you are unsure, consult your doctor or pharmacist. Take the medicine orally after meals. Do not take the medicine immediately before bed. Adults and children over 12 years old. years: initially, for 2–3 days, take 30 mg of ambroxol hydrochloride (5 ml of syrup, i.e. 1 measuring spoon) 3 times a day; then the dose should be reduced to 30 mg (5 ml syrup, i.e. 1 measuring spoon) 2 times a day. Children aged 6 to 12 years: 15 mg ambroxol hydrochloride (2.5 ml syrup, i.e. half measuring spoon) 2 times. up to 3 times a day. Children aged 2 to 6 years: 7.5 mg ambroxol hydrochloride (1.25 ml syrup, i.e. ¼ scoop) 3 times a day. Do not use in children without consulting a doctor. If treatment continues for longer than 7–14 days, the dose should be reduced. If symptoms worsen or do not improve after 4–5 days, consult a doctor. This medicine does not contain sucrose. If you have the impression that the effect of Ambrosol Teva is too strong or too weak, consult a doctor. If you take more Ambrosol Teva than you should; At the moment, a person does not have specific symptoms of an overdose. If you take more Ambrosol Teva than you should, you may experience the symptoms listed in section 4.” Possible side effects.” Symptomatic treatment is recommended. In young children and patients with a weakened cough reflex (elderly people, unconscious people), ensure the removal of bronchial secretions from the respiratory tract. If you take a dose of the drug that exceeds the recommended one, you should consult a doctor or contact your pharmacist immediately. If you forget to take Ambrosol Teva: If you miss a dose, take it as soon as you remember, and then resume your regular dosing schedule. Do not take a double dose to make up for a missed dose. If you have any additional questions about the use of this medication, ask your doctor.
Contraindications
If you are allergic (hypersensitive) to ambroxol hydrochloride, bromhexine or any of the excipients listed in section 6.1. If you have a rare hereditary intolerance to excipients (see also the section “Teva Ambrosol contains methyl parahydroxybenzoate and propyl parahydroxybenzoate, propylene glycol, sorbitol”). .In children under 2 years of age.
Side effects
Like all medicines, Ambrosol Teva can cause side effects, although not everyone gets them. The following side effects may occur: Common (may affect up to 1 in 10 people):
taste disturbances (eg, taste changes), nausea, decreased sensation (hypesthesia) in the mouth and throat. Uncommon (may affect up to 1 in 100 people):
vomiting, diarrhea, abdominal pain, upset stomach, dry mouth. Rare (may affect up to 1 in 1000 people):
hypersensitivity reactions,
rash, hives,
heartburn. Frequency unknown (frequency cannot be estimated from available data):
anaphylactic reactions, including anaphylactic shock, angioedema (rapidly progressive swelling of the skin, subcutaneous tissue, mucous membrane or submucosal tissue) and itching;
serious skin side effects (including erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis and acute generalized pustulosis)
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