Bromhexine 8mg tablets
Requires a prescription from a doctor or prescriber
Bromhexine is mucolytic agent used for a variety of respiratory conditions associated with increased mucus secretion.
Official documents, adverse reaction reporting, and safety monitoring
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Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Bromhexine
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Submit a Yellow Card report to the MHRA
Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Bromhexine
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
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Supply & safety information
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 9 · Randomised trials: 12 · 2017–2026
Showing the 50 most relevant studies, sorted by most relevant.
McCullough B, Busby J, O'Neill B, et al.
2026
- Lung
- Bronchiectasis
- Expectorants
BackgroundMucoactive agents aim to improve mucociliary clearance in bronchiectasis, disrupting the cycle of impaired clearance, infection and inflammation. Registry data show 28% of patients use these agents, but prescribing varies due to limited evidence. We aimed to update evidence on mucoactive agents' effects in adults with bronchiectasis.MethodsWe conducted a systematic review and meta-analysis, searching Medline, Embase, CENTRAL and trial registries to 1 October 2025. Eligible studies included adults with bronchiectasis, evaluating any mucoactive agent versus placebo or control. Cystic fibrosis and paediatric studies were excluded. The primary outcome was exacerbation frequency; secondary outcomes included lung function, quality of life and adverse events.FindingsFrom 1512 records, 24 studies (20 randomised, four observational: n=7051) evaluated eight mucoactive agents (ambroxol, bromhexine, carbocisteine, erdosteine, hypertonic saline, mannitol, N-acetylcysteine, rhDNase). Most trials had high or some risk of bias. Seven randomised studies (n=1259) reported exacerbations; pooled analysis did not demonstrate a statistically significant difference in annualised exacerbation incidence (mean difference -0.40 per patient per year, 95% CI -1.04-0.24; p=0.22; I2=91%; very low certainty). Nine studies (n=767) reported percent predicted forced expiratory volume in 1 s (FEV1 % pred), showing a small mean increase of 3.23% (95% CI 0.31-6.15; p=0.03; I2=69.9%; very low certainty). Pooled analyses did not demonstrate significant differences for other spirometry measures, quality of life or adverse events.InterpretationPooled evidence did not show a reduction in exacerbations and FEV1 % pred improvements were small. Evidence certainty was low/very low, meaning overall clinical benefit remains uncertain, highlighting the need for targeted trials of specific agents and subgroups.
Abstract licence: CC BY
K. Ansarin, R. Tolouian, M. Ardalan, et al.
BioImpacts : BI, 2020
Fariz Nurwidya
MEDICINUS, 2025
Yuying Wang, Yinghu Zhang, Xia Chen, et al.
Medicine, 2020
D. Wannigama, Cameron Hurst, P. Phattharapornjaroen, et al.
eClinicalMedicine, 2024
M.K.E. Ogbac, J. E. Tamayo, Johnny Siu, et al.
Respirology (Carlton, Vic.), 2021
A. Eslami Ghayour, S. Nazari, F. Keramat, et al.
Revista clinica espanola, 2024
- Bromhexine
- COVID-19
- Acetylcysteine
Ramírez D, Rojas R, Fierro H, et al.
2024
- Bromhexine
- Expectorants
- COVID-19 Drug Treatment
Humberto Fierro, Daniela Alejandra Nova, Estibaliz Ampuero, et al.
Open Science Framework, 2024
Ghayour AE, Nazari S, Keramat F, et al.
2023
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
31.4 hours
Mechanism
Inflammation of the airways, increased mucus secretion, and altered mucociliary…
Food interactions
None known
Human targets
2 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
8-32 mg
Half-life
32 mg
[L33060]
Protein binding
95%
[L33060]
Volume of distribution
206 L
Metabolism
Elimination
97%
[L33060]
…
Clearance
843-1073 mL/min
[L33060]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L29975][L24819][L33060]
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 328 interactions
[L33125]
The observed symptoms of accidental overdose with bromhexine are consistent with the
known adverse effects of bromhexine, including headache, nausea, and vomiting, among other symptoms. Provide symptomatic treatment and contact poison control services if an overdose is confirmed or suspected.
[L33060]
Recent have studies have demonstrated that bromhexine inhibits the transmembrane serine protease 2 receptor (TMPRSS2) in humans. Activation of TMPRSS2 plays an important role in viral respiratory diseases such as influenza A and Middle East Respiratory Syndrome (MERS). Inhibition of receptor activation and viral entry by bromhexine may be effective in preventing or treating various respiratory illnesses, including COVID-19.[A233345][A233350] In vitro studies have suggested the action of ambroxol (a metabolite of bromhexine) on the angiogensin-converting enzyme receptor 2 (ACE2), prevents entry of the viral envelope-anchored spike glycoprotein of SARS-Cov-2 into alveolar cells or increases the secretion of surfactant, preventing viral entry.[A233365 ,A233370]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[A233285][L33060]
The bioavailability is therefore reduced to approximately 22-27%.
[L33060]
[L33060]
[L33060]
Lung tissue concentrations of bromhexine two hours after a dose were 1.5 to 3.2 times higher in bronchial tissues than plasma concentrations. Pulmonary parynchema concentrations were 3.4 to 5.9 times higher when compared to plasma concentrations.
[L33060]
[L33060]
In one study of human plasma, (E)-4-hydroxydemethylbromhexine (E-4-HDMB) and (E)-3-hydroxydemethylbromhexine (E-3-HDMB) were quantified as major metabolites of ambroxol, and (Z)-4-hydroxydemethylbromhexine and (Z)-3-hydroxydemethylbromhexine were quantified as minor metabolites.
[A233340]
[L33060]
[L33060]
Proteins and enzymes this drug interacts with in the body
PMID:32703818 PMID:35676539 PMID:37990007 PMID:38964328
Participates in proteolytic cascades of relevance for the normal physiologic function of the prostate .
PMID:25122198
Androgen-induced TMPRSS2 activates several substrates that include pro-hepatocyte growth factor/HGF, the protease activated receptor-2/F2RL1 or matriptase/ST14 leading to extracellular matrix disruption and metastasis of prostate cancer cells .
PMID:15537383 PMID:25122198 PMID:26018085
In addition, activates trigeminal neurons and contribute to both spontaneous pain and mechanical allodynia (By similarity)
PMID:27217402
Converts angiotensin I to angiotensin 1-9, a nine-amino acid peptide with anti-hypertrophic effects in cardiomyocytes, and angiotensin II to angiotensin 1-7, which then acts as a beneficial vasodilator and anti-proliferation agent, counterbalancing the actions of the vasoconstrictor angiotensin II .
PMID:10924499 PMID:10969042 PMID:11815627 PMID:14504186 PMID:19021774
Also removes the C-terminal residue from three other vasoactive peptides, neurotensin, kinetensin, and des-Arg bradykinin, but is not active on bradykinin .
PMID:10969042 PMID:11815627
Also cleaves other biological peptides, such as apelins (apelin-13, [Pyr1]apelin-13, apelin-17, apelin-36), casomorphins (beta-casomorphin-7, neocasomorphin) and dynorphin A with high efficiency .
PMID:11815627 PMID:27217402 PMID:28293165
In addition, ACE2 C-terminus is homologous to collectrin and is responsible for the trafficking of the neutral amino acid transporter SL6A19 to the plasma membrane of gut epithelial cells via direct interaction, regulating its expression on the cell surface and its catalytic activity PMID:18424768 PMID:19185582
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC R05CB02
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Bromhexine
Additional database identifiers
ChemSpider
2348
BindingDB
50239965
ZINC
ZINC000000608220
HUGO Gene Nomenclature Committee (HGNC)
HGNC:11876
GeneCards
TMPRSS2
Guide to Pharmacology
2421
UniProt Accession
TMPS2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:13557
GenAtlas
ACE2
GeneCards
ACE2
GenBank Gene Database
AF291820
GenBank Protein Database
9802433
Guide to Pharmacology
1614
UniProt Accession
ACE2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:13557
GenAtlas
ACE2
GeneCards
ACE2
GenBank Gene Database
AF291820
GenBank Protein Database
9802433
Guide to Pharmacology
1614
UniProt Accession
ACE2_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72