Bromhexine | Bromhexine tablets 8 mg 50 pcs.
Special Price
$13.72
Regular Price
$21.00
In stock
SKU
BID494189
Release form
Tablets
Tablets
Release form
Tablets
Packaging
50 units
Pharmacological action
Bromhexine has a mucolytic (secretolytic) and expectorant effect. The mucolytic effect is associated with the depolymerization and liquefaction of mucoprotein and mucopolysaccharide fibers. Bromhexine has a weak antitussive effect. It stimulates the production of endogenous surfactant, which ensures the stability of alveolar cells during respiration. The clinical effect is manifested after 2-5 days from the start of treatment with the drug.
Pharmacokinetics
When taken orally, bromhexine is almost completely absorbed (99%) within 30 minutes. Bioavailability is 20-25% (effect of the first passage through the liver). In plasma, bromhexine firmly binds to 95% proteins, penetrates the blood-brain and placental barriers. In the liver, bromhexine undergoes demethylation and oxidation. The half-life is 15 hours due to slow back diffusion from the tissues. It is excreted by the kidneys. In chronic renal failure, the excretion of bromhexine metabolites is impaired. With repeated use, bromhexine can accumulate.
Indications
Secretolytic therapy of acute and chronic bronchopulmonary diseases accompanied by impaired sputum formation and transport.
Contraindications
Hypersensitivity to bromhexine and / or to any auxiliary component of the drug, including lactose and sucrose, gastric ulcer and 12 duodenal ulcer in the acute phase, pregnancy (I trimester), lactation, childhood (up to 3 years).
Use during pregnancy and lactation
During pregnancy and lactation, bromhexine is used in cases where the expected benefits to the mother outweigh the potential risk to the fetus or baby.
Special instructions
For gastric ulcer, as well as for indications of a history of gastric bleeding, bromhexine should be used under medical supervision.
Use with caution in patients with bronchial asthma.
Bromhexine is not used concurrently with medicines containing codeine, because this makes it difficult to cough up liquefied sputum.
Used as part of combined herbal preparations with essential oils (including with eucalyptus oil, anise oil, peppermint oil, menthol).
Composition
1 tablet contains:
active ingredient - bromhexine hydrochloride - 8 mg
excipients: sucrose, lactose monohydrate, potato starch, stearic acid 95, microcrystalline cellulose type 101.
Dosage and administration
Tablets should be taken orally, after meals, with plenty of fluids.
Adults and adolescents over 14 years of age are prescribed 1 to 2 tablets (8 to 16 mg) 3 times a day.
Children and adolescents from 6 to 14 years old, as well as persons weighing less than 50 kg, 1 tablet (8 mg) 3 times a day. Children under 6 years of age should take lower dosage forms.
Children under 6 years of age should take lower dosage dosage forms of bromhexine and only on the advice of a doctor.
Therapeutic effect may occur on day 4-6. The course of treatment is from 4 to 28 days (determined individually depending on the indications and course of the disease). Patients with renal failure or impaired liver function are prescribed lower doses or increase the interval between doses.
Side effects of the
From the digestive system: dyspeptic symptoms, transient increase in the activity of hepatic transaminases in the blood serum.
From the side of the central nervous system: headache, dizziness.
Dermatological reactions: increased sweating, skin rash.
From the respiratory system: cough, bronchospasm.
Drug Interactions
Bromhexine can be prescribed concurrently with other drugs used in the treatment of bronchopulmonary diseases.
Bromhexine is not prescribed simultaneously with antitussive drugs (including those containing codeine), because they may make it difficult to cough up Bromhexine-diluted sputum.
Bromhexine promotes the penetration of antibiotics (amoxicillin, erythromycin, cephalexin, oxytetracycline), sulfonamide drugs into bronchial secretion in the first 4-5 days of antimicrobial therapy.
Bromhexine is not compatible with alkaline solutions.
Overdose
Symptoms: nausea, vomiting, diarrhea, dyspeptic disorders.
Treatment: artificial vomiting, gastric lavage (in the first 1-2 h after admission).
Storage conditions
Store at a temperature not exceeding 25 РC.
shelf life
5 years
Deystvuyushtee substance
Bromgeksin
Conditions of sale from
pharmacies Without prescription
Dosage form
tablets
Prescribing
Prescribing
For adults, Pregnant women II and III trimester as prescribed by a doctor, Children over 3 years old
Borisov factory, Belarus
Tablets
Packaging
50 units
Pharmacological action
Bromhexine has a mucolytic (secretolytic) and expectorant effect. The mucolytic effect is associated with the depolymerization and liquefaction of mucoprotein and mucopolysaccharide fibers. Bromhexine has a weak antitussive effect. It stimulates the production of endogenous surfactant, which ensures the stability of alveolar cells during respiration. The clinical effect is manifested after 2-5 days from the start of treatment with the drug.
Pharmacokinetics
When taken orally, bromhexine is almost completely absorbed (99%) within 30 minutes. Bioavailability is 20-25% (effect of the first passage through the liver). In plasma, bromhexine firmly binds to 95% proteins, penetrates the blood-brain and placental barriers. In the liver, bromhexine undergoes demethylation and oxidation. The half-life is 15 hours due to slow back diffusion from the tissues. It is excreted by the kidneys. In chronic renal failure, the excretion of bromhexine metabolites is impaired. With repeated use, bromhexine can accumulate.
Indications
Secretolytic therapy of acute and chronic bronchopulmonary diseases accompanied by impaired sputum formation and transport.
Contraindications
Hypersensitivity to bromhexine and / or to any auxiliary component of the drug, including lactose and sucrose, gastric ulcer and 12 duodenal ulcer in the acute phase, pregnancy (I trimester), lactation, childhood (up to 3 years).
Use during pregnancy and lactation
During pregnancy and lactation, bromhexine is used in cases where the expected benefits to the mother outweigh the potential risk to the fetus or baby.
Special instructions
For gastric ulcer, as well as for indications of a history of gastric bleeding, bromhexine should be used under medical supervision.
Use with caution in patients with bronchial asthma.
Bromhexine is not used concurrently with medicines containing codeine, because this makes it difficult to cough up liquefied sputum.
Used as part of combined herbal preparations with essential oils (including with eucalyptus oil, anise oil, peppermint oil, menthol).
Composition
1 tablet contains:
active ingredient - bromhexine hydrochloride - 8 mg
excipients: sucrose, lactose monohydrate, potato starch, stearic acid 95, microcrystalline cellulose type 101.
Dosage and administration
Tablets should be taken orally, after meals, with plenty of fluids.
Adults and adolescents over 14 years of age are prescribed 1 to 2 tablets (8 to 16 mg) 3 times a day.
Children and adolescents from 6 to 14 years old, as well as persons weighing less than 50 kg, 1 tablet (8 mg) 3 times a day. Children under 6 years of age should take lower dosage forms.
Children under 6 years of age should take lower dosage dosage forms of bromhexine and only on the advice of a doctor.
Therapeutic effect may occur on day 4-6. The course of treatment is from 4 to 28 days (determined individually depending on the indications and course of the disease). Patients with renal failure or impaired liver function are prescribed lower doses or increase the interval between doses.
Side effects of the
From the digestive system: dyspeptic symptoms, transient increase in the activity of hepatic transaminases in the blood serum.
From the side of the central nervous system: headache, dizziness.
Dermatological reactions: increased sweating, skin rash.
From the respiratory system: cough, bronchospasm.
Drug Interactions
Bromhexine can be prescribed concurrently with other drugs used in the treatment of bronchopulmonary diseases.
Bromhexine is not prescribed simultaneously with antitussive drugs (including those containing codeine), because they may make it difficult to cough up Bromhexine-diluted sputum.
Bromhexine promotes the penetration of antibiotics (amoxicillin, erythromycin, cephalexin, oxytetracycline), sulfonamide drugs into bronchial secretion in the first 4-5 days of antimicrobial therapy.
Bromhexine is not compatible with alkaline solutions.
Overdose
Symptoms: nausea, vomiting, diarrhea, dyspeptic disorders.
Treatment: artificial vomiting, gastric lavage (in the first 1-2 h after admission).
Storage conditions
Store at a temperature not exceeding 25 РC.
shelf life
5 years
Deystvuyushtee substance
Bromgeksin
Conditions of sale from
pharmacies Without prescription
Dosage form
tablets
Prescribing
Prescribing
For adults, Pregnant women II and III trimester as prescribed by a doctor, Children over 3 years old
Borisov factory, Belarus
Write Your Own Review