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Bronchostop (Syrup) Instructions for Use

Marketing Authorization Holder

Slavic Pharmacy, LLC (Russia)

ATC Code

R05CB02 (Bromhexine)

Active Substance

Bromhexine (Rec.INN registered by WHO)

Dosage Form

Bottle OTC Icon Bronchostop Syrup 4 mg/5 ml: 100 ml bottle

Dosage Form, Packaging, and Composition

Syrup 5 ml
Bromhexine hydrochloride 4 mg

100 ml – polyethylene terephthalate bottles (1) with a dosing spoon or cup – cardboard packs.
100 ml – dark glass bottles (1) with a dosing spoon or cup – cardboard packs.

Clinical-Pharmacological Group

Mucolytic and expectorant drug

Pharmacotherapeutic Group

Mucolytic agent

Pharmacological Action

Mucolytic agent with expectorant action. It reduces the viscosity of bronchial secretions by depolymerizing the acidic polysaccharides contained in it and by stimulating the secretory cells of the bronchial mucosa that produce secretions containing neutral polysaccharides.

It is believed that Bromhexine promotes the formation of surfactant.

Pharmacokinetics

Bromhexine is rapidly absorbed from the gastrointestinal tract and undergoes intensive metabolism during the first pass through the liver. Its bioavailability is about 20%. In healthy patients, the Cmax in plasma is determined after 1 hour.

It is widely distributed in body tissues. About 85-90% is excreted in the urine, mainly in the form of metabolites. The metabolite of bromhexine is ambroxol.

The binding of bromhexine to plasma proteins is high. The T1/2 in the terminal phase is about 12 hours.

Bromhexine penetrates the blood-brain barrier. It penetrates the placental barrier in small amounts.

Only small amounts are excreted in the urine with a T1/2 of 6.5 hours.

The clearance of bromhexine or its metabolites may be reduced in patients with severe hepatic and renal impairment.

Indications

Diseases of the respiratory tract accompanied by the formation of difficult-to-separate viscous secretions: tracheobronchitis, chronic bronchitis with a broncho-obstructive component, bronchial asthma, cystic fibrosis, chronic pneumonia.

ICD codes

ICD-10 code Indication
E84 Cystic fibrosis
J04 Acute laryngitis and tracheitis
J15 Bacterial pneumonia, not elsewhere classified
J20 Acute bronchitis
J37 Chronic laryngitis and laryngotracheitis
J42 Unspecified chronic bronchitis
J44 Other chronic obstructive pulmonary disease
J45 Asthma
R05 Cough
ICD-11 code Indication
CA05 Acute laryngitis or tracheitis
CA0G Chronic laryngitis or laryngotracheitis
CA20.1Z Chronic bronchitis, unspecified
CA22.Z Chronic obstructive pulmonary disease, unspecified
CA23 Asthma
CA25.Z Cystic fibrosis, unspecified
CA40.0Z Bacterial pneumonia, unspecified
CA42.Z Acute bronchitis, unspecified
MD12 Cough

Dosage Regimen

The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen.

Orally for adults and children over 10 years old – 8 mg 3-4 times/day. For children under 2 years old – 2 mg 3 times/day; for ages from 2 to 6 years – 4 mg 3 times/day; for ages from 6 to 10 years – 6-8 mg 3 times/day.

If necessary, the dose can be increased for adults to 16 mg 4 times/day, for children – to 16 mg 2 times/day.

In the form of inhalations for adults – 8 mg, for children over 10 years old – 4 mg, for ages 6-10 years – 2 mg. For children under 6 years old – used in doses up to 2 mg. Inhalations are performed 2 times/day.

The therapeutic effect may appear on the 4th-6th day of treatment.

Parenteral administration is recommended for treatment in severe cases, as well as in the postoperative period to prevent the accumulation of thick sputum in the bronchi. Administer 2 mg subcutaneously, intramuscularly, or intravenously 2-3 times/day slowly over 2-3 minutes.

Adverse Reactions

From the digestive system: dyspeptic phenomena, transient increase in the activity of liver transaminases in the blood serum.

From the central nervous system: headache, dizziness.

Dermatological reactions: increased sweating, skin rash.

From the respiratory system: cough, bronchospasm.

Contraindications

Hypersensitivity to bromhexine.

Use in Pregnancy and Lactation

Contraindicated in the first trimester of pregnancy. Use in the second and third trimesters of pregnancy and during breastfeeding is possible only in cases where the intended benefit to the mother outweighs the potential risk to the fetus or infant.

Use in Hepatic Impairment

Should be used with caution in patients with impaired liver function.

Use in Renal Impairment

Should be used with caution in patients with impaired renal function.

Pediatric Use

Use with caution in children – according to indications, in age-appropriate recommended doses and dosage forms.

Special Precautions

In case of gastric ulcer, as well as with a history of gastric bleeding, Bromhexine should be used under medical supervision.

Use with caution in patients suffering from bronchial asthma.

Bromhexine should not be used simultaneously with medicines containing codeine, as this makes it difficult to cough up liquefied sputum.

It is used as part of combined herbal preparations with essential oils (including eucalyptus oil, anise oil, peppermint oil, menthol).

Drug Interactions

Bromhexine is incompatible with alkaline solutions.

Storage Conditions

Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.

Dispensing Status

Over-the-Counter

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.

Medical Disclaimer

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