Bismuth subgallate 300mg suppositories
Requires a prescription from a doctor or prescriber
Bismuth subgallate is a yellow colored substance that presents as an odorless powder that undergoes discoloration when exposed to sunlight.
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Suspected adverse reactions reported for Bismuth subgallate
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4 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.
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Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. 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: 18 · Randomised trials: 3 · 1964–2026
Showing the 50 most relevant studies, sorted by most relevant.
Alexander C. Ford, Peter Malfertheiner, Monique Giguère, et al.
World Journal of Gastroenterology, 2008
- Helicobacter pylori
- Anti-Bacterial Agents
- Bismuth
I. Witting, Thomas C. Chasapis, F. Ricci, et al.
Advanced Electronic Materials, 2019
M. Shahbazi, L. Faghfouri, Mónica P. A. Ferreira, et al.
Chemical Society reviews, 2020
Peipei Dang, Dongjie Liu, Guogang Li, et al.
Advanced Optical Materials, 2020
Sherwood L. Gorbach
Gastroenterology, 1990
- Bismuth
- Campylobacter
- Chemistry
J. Gou, Hua Bai, Xuanlin Zhang, et al.
Nature, 2023
José M. Brum, Roger Gibb, David L. Ramsey, et al.
Digestive Diseases and Sciences, 2020
- Bismuth
- Communicable Diseases
- Diarrhea
Hye-Won Moon, Josep Cornella
ACS Catalysis, 2022
F. Schindler, Zhijun Wang, M. Vergniory, et al.
Nature physics, 2018
Na Han, Yu Wang, Hui Yang, et al.
Nature Communications, 2018
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
21-72 days
Mechanism
Bismuth salts exert their action largely in the upper gastrointestinal tract by…
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
0.04%
[L2314]…
Half-life
21-72 days
[L2330]
Protein binding
90%
Volume of distribution
Metabolism
[L2314]
In the kidney it induces the de novo synthesis of a bismuth-metal-binding protein, which is a kind of methallothionein .
[L2314]…
Elimination
24 hours
[L2314]…
Clearance
50 to 95 ml/min
[A32583]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L2309][L2312][A32566]
Additionally, there are also various non-prescription (over the counter) bismuth subgallate based wound healing products as well as ongoing studies into whether or not the substance can be utilized as a legitimate hemostatic agent - usually for soft tissue surgery in otorhinolaryngology and/or dermatologic settings .
[A32567][A32568][A32569][A32570]
Moreover, in the past bismuth subgallate may have seen some use as a treatment for Helicobacter pylori infection .
[A32571]
In contrast, contemporary first-line therapies generally involve proton pump inhibitor and antibiotic combination therapies that generally achieve high rates of pathogen eradication, ease of administration, and patient compliance.
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 852 interactions
[A32571]
Similarly, because of the biliary excretion of bismuth, severe liver disease may theoretically result in accumulation of bismuth as well .
[A32571]
Bismuth toxicity seemingly develops only from excessive dosage (perhaps from ingestion of bismuth over a prolonged time or intramuscular injections) and is characterized by nephrotoxicity, osteoarthropathy, encephalopathy, hepatotoxicity, stomatitis, and gingivitis .
[A32571]
However, the insoluble inorganic bismuth compounds are reported to be mainly associated with reversible encephalopathy .
[A32571]
In fact a number of studies have discussed how patients may experience a syndrome of subacute, progressive encephalopathy involving potential aphasia, myoclonous, and/or gait instability after taking bismuth subgallate in large quantities well over the usual recommended dosages .
[A32586][A32587]
This kind of encephalopathy is usually reversible with the discontinuation of the bismuth subgallate usage however .
[A32586][A32587]
In terms of bismuth subgallate's ability to deodorize flatulence and stools as an internal deodorant - although not fully elucidated - it is believed that when the substance is administered orally, its relative insolubility and poor absorption allows it to remain within the gastrointestinal lumen and inhibit colonic bacteria from acting on fermentable food residues in the GI tract [L2314].
Moreover, when bismuth subgallate is taken orally, various salts like bismuth citrate, bismuth oxychloride, and others are formed [A32571]. These salts are then taken up into surrounding gastric mucus as well as bound to protein within the base of any ulcers that may be present after coming into contact with gastric juice [A32571]. Additionally, bismuth compounds like bismuth subgallate are also believed to have the capacity to trigger the secretion of prostaglandins, epithelial growth factor (EGF), and mucosal bicarbonate as a means to inhibit the action of pepsin in gastric juice [A32571]. These actions subsequently protect gastric mucous from peptic luminal degradation as well as enhance the properties of mucous to assist in the healing of both duodenal and gastric ulcers [A32571]. In this way, bismuth subgallate works to absorb extra water and/or toxins in the large intestine, allowing it to form a protective coat on the intestinal mucosa and over ulcers that may or may not be associated with infections like those of Helicobacter pylori [L2312].
Furthermore, studies have shown that bismuth compounds like bismuth subgallate are capable of demonstrating antimicrobial effects against various gastrointestinal tract pathogens like E. coli, Salmonella, Shigella, Vibrio cholera, Campylobacter jejuni, H. pylori, and some enteric viruses like Rotaviruses [A32571]. Although the exact mechanism(s) of action by which bismuth compounds are able to elicit such antimicrobial effects remains unclear [A32571], a number of experimental observations suggest that bismuth has been able to complex with the bacterial wall and periplasmic membrane; inhibit bacterial enzymes like urease, catalase, and lipase; inhibit bacterial protein and ATP synthesis; and also inhibit or decrease the adherence of bacteria like H. pylori to epithelial cells [A32571]. In essence, ultrastructural studies have shown evidence of the binding of bismuth complexes to the bacterial wall and periplasmic space between the inner and outer bacterial membrane of H.pylori with subsequent ballooning and disintegration of the pathogen [A32571]. To various extents, these antimicrobial actions may also illustrate how bismuth subgallate is capable of neutralizing colonic bacteria from acting on fermentable foods as well.
Numerous studies have and continue to study the possible hemostatic action that bismuth subgallate may have. As the bismuth salt of gallic acid, bismuth subgallate's chemical structure shares similarities to ellagic acid, another gallic acid derivative [A32572]. Ellagic acid itself is a clot-promoting agent that initiates thrombin formation by way of the intrinsic pathway via an action on Hageman factor (clotting factor XII) [A32572][A32569]. It is believed that bismuth subgallate's ability to activate factor XII is associated with the chemical's negatively charged moieties - whose contact with factor XII would theoretically initiate the intrinsic pathway to blood clotting [A32572].
Other studies have also suggested that bismuth subgallate is capable of inducing macrophages to secrete growth factors to facilitate wound healing, decreasing lesion area, enhancing granulation tissue formation and re-epithelialization, the initiation of the proliferation of collagen via the activation of fibroblasts, the accelerated re-establishment of blood vessels, and also the restriction of nitric oxide formation [A32570][A32578].
Given such studies regarding bismuth subgallate's potential hemostatic abilities, there has been and continues to be interest in indicating the agent for use in otolaryngology as in tonsillectomies or adenotonsillectomies to achieve reduced bleeding and surgery times; topical treatment in various open wound surgeries to facilitate faster and earlier clotting between tissues; ileostomy; dental surgeries; epistaxis management; among others [A32567][A32569]. Nevertheless, study results are conflicting; where there may be experimental results suggesting some improvements in reduced operation time and operative blood loss when bismuth subgallate is used as a hemostatic agent in tonsillectomies [A32572] there are also study results that observed bismuth subgallate having a negative influence on the healing processes of wounds inflicted in animal models, in which the use of the agent actually delayed the rate of new vessel formation and optimal wound healing [A32569].
Finally, bismuth subgallate also demonstrates a strong astringent ability [A32569] - an action that can facilitate both its deodorant and hemostatic effects and assists in its indication as an active ingredient in a number of non-prescription products for hemorrhoid suppositories or topical applications, diarrhea, etc [L2314].
Additionally, like other bismuth agents, one of the most common side effects associated with bismuth subgallate is its propensity to cause a black discoloration of the tongue and stools when the agent combines with trace amounts of sulfur in the saliva and/or gastrointestinal tract [L2316]. This discoloration is temporary and harmless, gradually dissipating over a number of days and eventually disappearing after the discontinuation of the bismuth agent [L2316].
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L2314]
The general human oral bioavailability of bismuth subgallate has been reported as low as 0.04% .
[L2314]
Any absorption that does occur is likely to happen from the upper small intestine .
[A32571]
The gastrointestinal absorption of bismuth from bismuth compounds demonstrates a large interindividual variation .
[L2314]
Factors affecting the absorption involve the formulation of the bismuth subgallate compound as well as the dietary factors of the individuals themselves .
[A32571]
Nevertheless, absorption can be enhanced with the concomitant intake of citrate and sulfhydryl-group-containing compounds .
[L2314]
Conversely, the simultaneous administration of antacids or a diet that is high in thiol content can lower absorption of bismuth subgallate .
[A32571]
[L2330]
[L2314]
The bismuth component itself is generally known to demonstrate a high percentage binding to plasma proteins of >90% .
[L2330]
[L2314]
In the kidney it induces the de novo synthesis of a bismuth-metal-binding protein, which is a kind of methallothionein .
[L2314]
[L2314]
Any absorbed bismuth is eliminated from the body by both the urinary and faecal (including bile) routes .
[L2314]
Excretion of absorbed bismuth in the urine is rapid, with most of the metal excreted within 24 hours .
[A32571]
About 10% of the absorbed bismuth is detected in faeces, presumably owing to biliary secretion .
[A32571]
[A32583]
Proteins that carry this drug through the body
PMID:19021548
Major calcium and magnesium transporter in plasma, binds approximately 45% of circulating calcium and magnesium in plasma (By similarity).
Potentially has more than two calcium-binding sites and might additionally bind calcium in a non-specific manner (By similarity). The shared binding site between zinc and calcium at residue Asp-273 suggests a crosstalk between zinc and calcium transport in the blood (By similarity). The rank order of affinity is zinc > calcium > magnesium (By similarity).
Binds to the bacterial siderophore enterobactin and inhibits enterobactin-mediated iron uptake of E.coli from ferric transferrin, and may thereby limit the utilization of iron and growth of enteric bacteria such as E.coli .
PMID:6234017
Does not prevent iron uptake by the bacterial siderophore aerobactin PMID:6234017
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)
Bismuth subgallate
Additional database identifiers
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
Molecular structure

Linked open data from Wikidata (Q3757667), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. Molecular structure images from Wikimedia Commons.