Bromhexine syrup

Release form

Syrup 8 mg/5 ml or syrup 4 mg/5 ml. Transparent, colorless or slightly yellowish with the smell of vanillin.

Compound

Active ingredient : bromhexine hydrochloride (80 mg or 160 mg per 100 ml of syrup).

Excipients : propylene glycol, sodium benzoate, food grade sorbitol, citric acid monohydrate, saccharin (sodium saccharinate), vanillin, purified water.

Production

ROZFARM, LLC (Russia)
ROZLEKS PHARM, LLC (Russia)
Scan Biotech Ltd. (India)

Package

Syrup for oral administration, 50 ml or 100 ml in dark bottles made of polyethylene terephthalate or glass. Each bottle is placed together with instructions for use, a 5 ml measuring spoon or a 5 ml measuring cup in individual cardboard packs.

Pharmacological group

Mucolytic and expectorant drug

Action

Secretomotor, secretolytic, weak antitussive.

Bromhexine: description of the substance

Indications

Acute and chronic diseases of the respiratory tract, accompanied by difficulty in the discharge of viscous sputum: tracheobronchitis, bronchitis of various etiologies (including complicated by bronchiectasis), pneumonia, bronchial asthma, pulmonary tuberculosis, cystic fibrosis.

Sanitation of the bronchial tree in the preoperative period and during therapeutic and diagnostic intrabronchial manipulations, prevention of accumulation of thick viscous sputum in the bronchi after surgery.

Application and dosage

Inside. 1 measuring spoon or 1 measuring cup contains 5 ml of syrup.

Syrup 8 mg/5 ml is prescribed:

adults and children over 14 years old, 8–16 mg (5–10 ml) 3 times a day,
children 6–14 years old - 8 mg (5 ml) 3 times a day.

Syrup 4 mg/5 ml is prescribed to children in the following doses:

up to 2 years 2 mg (2.5 ml) 3 times a day,
2–6 years - 4 mg (5 ml) 3 times a day,
6–14 years - 8 mg (10 ml) 3 times a day.

Contraindications and restrictions

Hypersensitivity, peptic ulcer of the stomach and duodenum, pregnancy (first trimester), lactation period, children under 6 years of age (for syrup 8 mg/5 ml).

With caution : renal failure, liver failure, bronchial diseases accompanied by excessive accumulation of secretions, a history of gastrointestinal bleeding.

Side effects

Allergic reactions, nausea, vomiting, dyspepsia, exacerbation of gastric and duodenal ulcers, dizziness, headache, increased activity of liver transaminases (extremely rare).

Overdose

Symptoms: nausea, vomiting, diarrhea and other dyspeptic disorders. Treatment: artificial vomiting, gastric lavage (in the first 1–2 hours after administration).

special instructions

During treatment, it is necessary to consume a sufficient amount of fluid, which increases the expectorant effect of bromhexine.

Treatment should be combined with postural drainage or vibration massage of the chest, which facilitates the removal of secretions from the bronchi.

Bromhexine does not contain sugar; the syrup contains sweeteners, so it can be used in patients with diabetes and obesity.

Storage

Store in a dry place, protected from light, out of reach of children, at room temperature not lower than 15°C. Shelf life: 3 years.

Recipe

Available without a prescription.

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Trade name: Bromhexine 4 Berlin - Hemi

International nonproprietary name: bromhexine

Chemical name: N - (2-amino-3,5 - dibromobenzyl) - N - methylcyclohexanamine hydrochloride

Dosage form: oral solution

Composition per 100 ml solution:

Active ingredient: bromhexine hydrochloride – 0.08 g;

Excipients: propylene glycol, sorbitol, apricot-scented aromatic concentrate, hydrochloric acid 0.1 M (3.5%) solution, purified water.

Description: transparent, colorless, slightly viscous liquid with a characteristic apricot odor.

Pharmacotherapeutic group: expectorant mucolytic agent

ATX code: R05CB02

Pharmacological properties

Pharmacodynamics

Bromhexine has a mucolytic (secretolytic) and expectorant (secretomotor) effect. Reduces the viscosity of sputum; activates the ciliated epithelium, increases the volume of sputum and improves its discharge. Stimulates the production of endogenous surfactant, which ensures the stability of alveolar cells during respiration. The effect appears within 2-5 days from the start of treatment.

Pharmacokinetics

Suction. After oral administration, bromhexine is quickly and almost completely absorbed from the gastrointestinal tract. The half-life of absorption is about 0.4 hours. The maximum concentration in the blood plasma after oral administration is reached after 1 hour.

Distribution. The volume of distribution is approximately 7 l/kg body weight. The degree of binding to plasma proteins is 99%. Bromhexine penetrates the blood-brain barrier and the placental barrier. Penetrates into breast milk and cerebrospinal fluid. Bromhexine does not accumulate.

Metabolism. 80% of bromhexine undergoes a “first pass” effect through the liver with the formation of biologically active metabolites. In severe liver diseases, a decrease in the clearance of bromhexine is observed.

Excretion. Bromhexine is excreted from the body mainly in the form of metabolites. The half-life to achieve the minimum effective concentration after achieving equilibrium between the processes of absorption and excretion is approximately 1 hour. The final half-life is approximately 16 hours due to the reverse distribution of small amounts of bromhexine from tissues.

It is excreted primarily by the kidneys in the form of metabolites formed in the liver. Due to the high degree of binding to plasma proteins and the high volume of distribution, as well as the slow redistribution from tissues to the blood, significant elimination of bromhexine by dialysis or forced diuresis should not be expected.

In severe renal failure, an increase in the half-life of bromhexine metabolites cannot be excluded. Nitrosation of bromhexine is possible under physiological conditions in the stomach.

Indications for use

Secretolytic therapy for acute and chronic bronchopulmonary diseases associated with impaired secretion and transport of sputum (for example, acute and chronic bronchitis, bronchiectasis, tracheobronchitis, pneumonia, emphysema, cystic fibrosis, tuberculosis, pneumoconiosis).

Contraindications

hypersensitivity to bromhexine and other components of the drug;
peptic ulcer of the stomach and/or duodenum (including a history);
pregnancy (first trimester);
breastfeeding period;
children under 2 years of age;
congenital fructose intolerance.

Carefully

renal and/or liver failure;
in case of impaired bronchial motility, accompanied by excessive accumulation of secretions;
children aged from 2 to 6 years (used as prescribed by a doctor).

Use during pregnancy and breastfeeding

The use of the drug in the first trimester of pregnancy is contraindicated. In the second and third trimesters of pregnancy, the use of the drug is possible only if the expected benefit to the mother outweighs the possible risk to the fetus. The use of the drug during breastfeeding is contraindicated.

Directions for use and doses

Oral solution. 1 measuring spoon contains 5 ml of solution.

Unless otherwise prescribed, the following doses are recommended:

Adults and adolescents over 14 years of age: 3 times a day, 2-4 scoops (24-48 mg of bromhexine per day).

Children from 6 to 14 years of age, as well as patients weighing less than 50 kg: 3 times a day, 2 scoops (24 mg of bromhexine per day).

Children from 2 to 6 years: 3 times a day, 1 measuring spoon (12 mg of bromhexine per day) - used as prescribed by a doctor.

In case of impaired renal function and/or severe liver disease, the intervals between doses should be increased or the dose reduced. You should consult your doctor on this issue.

During therapy with Bromhexine 4 Berlin-Chemie, it is recommended to drink sufficient amounts of fluid.

Bromhexine 4 Berlin-Chemie should not be taken for more than 4-5 days without consulting your doctor. The duration of use is determined by the doctor individually and depends on the indications and course of the disease.

Side effect

Possible side effects are listed below in descending frequency of occurrence: very common (>1/10), common (>1/100, >1/10), uncommon (>1/1000, >1/100), rare (>1/100) 10000, <1/1000), very rare, including isolated reports (<1/10000), frequency not established (cannot be estimated from available data).

From the gastrointestinal tract

Uncommon: nausea, vomiting, diarrhea, abdominal pain;

From the immune system

Rarely: hypersensitivity reactions;

Frequency not established: anaphylactic reactions, including anaphylactic shock, angioedema, pruritus.

From the skin and subcutaneous tissues

Rarely: skin rash, urticaria;

Frequency not established: severe skin reactions, including erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell's syndrome), acute generalized exanthematous pustulosis (see section "Special instructions").

General violations

Uncommon: fever.

In case of all forms of allergic reactions (hypersensitivity, anaphylaxis) or in the event of any damage to the skin and/or mucous membranes, you must stop taking this drug and immediately inform your doctor.

Overdose

Life-threatening symptoms of overdose with Bromhexine 4 Berlin-Chemie are unknown.

Symptoms: A study of overdose cases has been published, according to which vomiting was observed in 4 out of 25 overdose cases. Three children experienced vomiting, as well as stunned consciousness, ataxia, diplopia, mild metabolic acidosis, and tachypnea. In children, symptoms did not occur when taking bromhexine at doses up to 40 mg, even in the absence of treatment.

There is no evidence of chronic toxicity of bromhexine in humans.

Treatment: in case of severe overdose, monitoring of blood circulation and, if necessary, symptomatic treatment are indicated. Due to the low toxicity of bromhexine, as a rule, there is no need for invasive measures aimed at reducing its absorption (forced vomiting, gastric lavage) or accelerating excretion. In addition, due to the pharmacokinetics (high volume of distribution, slow redistribution processes and high degree of protein binding), effective removal of bromhexine from the body by dialysis or forced diuresis should not be expected.

Since in children over 2 years of age, even after taking large doses of bromhexine, only mild symptoms are expected, with a dose of bromhexine hydrochloride up to 80 mg (for example, 100 ml of Bromhexine 4 Berlin-Chemie), detoxification may not be necessary. In younger children, the appropriate dose limit is 60 mg bromhexine hydrochloride (6 mg/kg body weight).

In case of overdose, it is also possible to develop side effects caused by excipients.

Interaction with other drugs

Bromhexine 4 Berlin-Chemie can be prescribed simultaneously with other drugs used in the treatment of bronchopulmonary diseases.

Bromhexine is not prescribed simultaneously with antitussives (including those containing codeine), because due to the suppression of the reflex, the evacuation of liquefied sputum is difficult, which can lead to the accumulation of secretions in the respiratory tract.

Bromhexine 4 Berlin-Chemie promotes the penetration of antibiotics (erythromycin, cephalexin, oxytetracycline, ampicillin, amoxicillin) into bronchial secretions in the first 4-5 days of antimicrobial therapy. The clinical significance of this possible interaction has not been proven.

When used simultaneously with drugs that irritate the gastrointestinal tract (for example, some non-steroidal anti-inflammatory drugs), the irritant effect of the latter on the gastric mucosa may be increased.

special instructions

In cases of impaired bronchial motility or with a significant volume of sputum secreted (for example, in the rare syndrome of primary ciliary dyskinesia), the use of Bromhexine 4 Berlin-Chemie requires caution due to the increased risk of airway obstruction.

In case of impaired renal function and severe liver disease, Bromhexine 4 Berlin-Chemie should be used with extreme caution (for example, it is recommended to reduce the dose or increase the intervals between doses). In severe renal failure, it is necessary to take into account the possibility of accumulation of metabolites formed in the liver.

Monitoring of liver function is recommended, especially during long-term treatment.

There is evidence of the occurrence in very rare cases of severe skin reactions (such as erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, acute generalized exanthematous pustulosis) while taking bromhexine.

If allergic reactions and/or signs of progressive skin rash occur (sometimes in combination with the appearance of blisters and damage to the mucous membranes), you should immediately stop using the drug and consult a doctor.

The use of Bromhexine 4 Berlin-Chemie in children over 2 years of age is possible only under the supervision of a physician.

Propylene glycol, which is part of the drug Bromhexine 4 Berlin-Chemie, can cause symptoms in children similar to those that occur after drinking alcohol.

Instructions for patients with diabetes: 5 ml of solution (1 scoop) contains 2 g of sorbitol (equivalent to 0.5 g of fructose), which corresponds to 0.17 bread units.

Sorbitol may have a slight laxative effect.

The effect of the drug on the ability to drive vehicles and machinery

When taken in recommended doses, Bromhexine 4 Berlin-Chemie does not affect the speed of psychomotor reactions.

Release form

Oral solution 4 mg/5 ml.

60 or 100 ml of solution in dark glass bottles with a screw-on plastic or aluminum stopper with a sealing gasket.

1 bottle complete with a measuring spoon along with instructions for use is placed in a cardboard box.

Storage conditions

At a temperature not higher than 25 oC.

Keep the medicine out of the reach of children!

Best before date

3 years.

3 months - after the first opening of the bottle.

Do not use after the expiration date stated on the packaging.

Vacation conditions

Available without a prescription.

Manufacturer

Berlin-Chemie AG

Glinker Weg, 125

12489 Berlin, Germany

Organization receiving complaints from consumers:

LLC "Berlin-Chemie/A. Menarini", Russia

123112, Moscow, Presnenskaya embankment, building 10, Business Center "Tower on the Embankment", Blok, tel., fax.