Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Bromhexine
Drug ID BADD_D00302
Description Bromhexine is mucolytic agent used for a variety of respiratory conditions associated with increased mucus secretion. It is derived from the Adhatoda vasica plant and aids in the clearance of excess mucus, improving breathing and reducing cough. It was introduced into the market in 1963, and is widely available as an over-the-counter drug in many countries.[A233240] Recently, bromhexine and its metabolite [ambroxol] have garnered interest for the potential prevention and treatment of COVID-19 due to their interactions with cell receptors in the lungs.[A233345,A233370]
Indications and Usage Bromohexine is used alone or with other ingredients such as [diphenhydramine], [dextromethorphan], and [guaifenesin] to reduce mucus viscosity and clear mucus in conditions associated with mucus hypersecretion, including the common cold, influenza, respiratory tract infections, or other conditions.[L29975,L24819,L33060]
Marketing Status approved
ATC Code R05CB02
DrugBank ID DB09019
KEGG ID D07542
MeSH ID D001964
PubChem ID 2442
TTD Drug ID D07UWJ
NDC Product Code Not Available
UNII Q1J152VB1P
Synonyms Bromhexine | Aparsonin | Bromhexin BC | BC, Bromhexin | Bromhexin Berlin-Chemie | Bromhexin Berlin Chemie | Bromhexin BerlinChemie | Bromhexine Hydrochloride | Hydrochloride, Bromhexine | Bromhexine Monohydrochloride | Monohydrochloride, Bromhexine | Brotussol | bromhexin von ct | ct, bromhexin von | von ct, bromhexin | Darolan | Dur-Elix | Dur Elix | DurElix | Famel Bromhexine | Bromhexine, Famel | Flegamin | Flubron | Hustentabs-ratiopharm | Hustentabs ratiopharm | Hustentabsratiopharm | Bromhexin-ratiopharm | Bromhexin ratiopharm | Bromhexinratiopharm | Mucohexine | NA-274 | NA 274 | NA274 | Tesacof | Bisolvon | Quentan | Bromhexin
Chemical Information
Molecular Formula C14H20Br2N2
CAS Registry Number 3572-43-8
SMILES CN(CC1=C(C(=CC(=C1)Br)Br)N)C2CCCCC2
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal pain upper07.01.05.003--
Anaphylactic shock10.01.07.002; 24.06.02.004---
Angioedema10.01.05.009; 22.04.02.008; 23.04.01.001---
Bronchospasm10.01.03.012; 22.03.01.004--
Dermatitis23.03.04.002---
Diarrhoea07.02.01.001--
Gastrointestinal disorder07.11.01.001---
Hypersensitivity10.01.03.003--
Immune system disorder10.02.01.001---
Nausea07.01.07.001--
Pruritus23.03.12.001--
Rash23.03.13.001---
Skin disorder23.03.03.007---
Urticaria10.01.06.001; 23.04.02.001--
Vomiting07.01.07.003--
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