Tropisetron 5mg capsules
Tropisetron is an indole derivative with antiemetic activity.
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Suspected adverse reactions reported for Tropisetron
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1 branded products available
WHO defined daily dose (DDD)
5 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary BNF/ATC mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
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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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: 5 · Randomised trials: 11 · 1994–2026
Showing the 50 most relevant studies, sorted by most relevant.
G. Bell, K. Caudle, Michelle Whirl‐Carrillo, et al.
Clinical pharmacology and therapeutics, 2017
Injeong Kim, G. Choi, Hyeon Joung Hwang, et al.
Journal of Personalized Medicine, 2024
Qiu N, Wang L, Chu R
2024
- Postoperative Nausea and Vomiting
- Antiemetics
- Cesarean Section
IntroductionSelective 5-hydroxytryptamine 3 receptor (5-HT3) antagonists are commonly used to prevent nausea and vomiting (NV) after cesarean section, but the comparative efficacy of different 5-HT3 antagonists remains unclear. This network meta-analysis aimed to determine which 5-HT3 antagonists might be the preferred choice for preventing NV in parturient scheduled for elective cesarean delivery under spinal anesthesia.Evidence acquisitionPubMed, EMBASE, Cochrane library, and Web of Science were searched for relevant randomized controlled trials (RCTs) published before August 24, 2023. Random network meta-analysis was performed using Stata 14.0 to estimate the efficacy of different 5-HT3 antagonists in preventing intra- and post-operative NV.Evidence synthesisTwenty-eight studies involving seven dosing regimens of three 5-HT3 antagonists were included. Pooled results showed that ondansetron 12 mg was superior to other six dosing regimens in the prevention of postoperative NV (PONV), PON, and POV, with the ranking probability of 80.2%, 95.8%, and 87.7%, respectively, followed by granisetron two mg. Ondansetron 4 mg might be the first choice for preventing intraoperative NV (IONV) (92.8%), with the least use of postoperative rescue antiemetics (90.6%). Granisetron 3 mg and tropisetron 2 mg might be the best options for preventing ION and IOV, respectively.ConclusionsBased on available data, ondansetron 12 mg may have the best efficacy in preventing PONV, PON, and POV. Additionally, more studies are warranted to compare the safety of ondansetron 12 mg versus granisetron two mg.
Abstract licence: CC BY-NC
Junli Liu, Mingming Liu, Shengnan Shi, et al.
Pain Reports, 2024
A. Shiina, Y. Shirayama, T. Niitsu, et al.
Annals of General Psychiatry, 2010
Mei Zhou, Shuo Yang, Rixin Chen, et al.
Zhongguo zhen jiu = Chinese acupuncture & moxibustion, 2024
- Nausea
- Vomiting
- Antineoplastic Agents
Hualin Chen, Liping Sun, Jijian Zheng, et al.
Frontiers in Medicine, 2025
BackgroundPostoperative nausea and vomiting (PONV) remain significant complications following pediatric adenotonsillectomy. Although palonosetron, a second-generation 5-HT3 receptor antagonist, has shown potential for preventing PONV, further research is needed to assess its efficacy when combined with dexamethasone in pediatric otolaryngologic procedures. This study aims to observe the efficacy of palonosetron or tropisetron combined with dexamethasone in preventing PONV in children undergoing adenotonsillectomy.MethodsWe enrolled 110 children scheduled for elective adenotonsillectomy under general anesthesia. Based on a computer-generated random number table, children were assigned in equal proportions to receive either palonosetron or tropisetron. The P-group received palonosetron (1 μg/kg, maximum 50 μg), while the T-group received tropisetron (0.1 mg/kg, maximum 2 mg) 5 min before anesthesia induction. After receiving their allocated drug, children received intravenous dexamethasone (0.15 mg/kg, maximum 5 mg) during induction. Primary outcomes included PONV incidence at 6, 24, and 48 h postoperatively. Secondary outcomes included the number of children with PONV scores of 1, 2, and 3, rescue antiemetic medication, and adverse events.ResultsA total of 110 children (aged 3–12 y, ASA physical status 1 or 2, weighted 14.3–47.3 kg) were enrolled in the study between December 2021 and July 2023. The P-group (n = 52) demonstrated significantly lower PONV incidence than the T-group (n = 51) during the 0–48 h (5.8% vs. 25.5%, p < 0.05). Notably, this difference was most pronounced during the first 24 h: 0–6 h (0% vs. 10%, p < 0.05) and 6–24 h (3.8% vs. 7.8%, p < 0.05). The difference during 24–48 h was insignificant (4% vs. 8%, p > 0.05). Transient junctional rhythm occurred in three patients receiving tropisetron, which did not affect circulation. Headache and dizziness were similar between groups within 48 h (P-group: 3.8%, T-group: 7.8%, p > 0.05).ConclusionIn pediatric adenotonsillectomy, palonosetron with dexamethasone gives better PONV prevention than tropisetron with dexamethasone, especially in the first 24 h, with comparable safety.Clinical trial registrationhttps://www.chictr.org.cn/showproj.html?proj=127115, ChiCTR2100046848.
Abstract licence: CC BY 4.0
Xie S, Huang R, Zhan Y, et al.
2023
- Nasopharyngeal Neoplasms
- Antiemetics
- Antineoplastic Agents
Mohammadreza Shalbafan, F. Malekpour, B. Tadayon Najafabadi, et al.
Journal of Psychopharmacology, 2019
L. Färber, T. Stratz, W. Brückle, et al.
International journal of clinical pharmacology research, 2001
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
2 found
Half-life
5.7 h
Mechanism
Tropisetron competitively binds to and blocks the action of serotonin at 5HT3 re…
Food interactions
1 warning
Human targets
2 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
20 minutes
Half-life
5.7 h
Protein binding
71%
Volume of distribution
400-600 L
Metabolism
Elimination
8%
Clearance
1800 ml/min
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Tropisetron appears to be well tolerated with the most frequently reported adverse effect being headache. Extrapyramidal side effects are rare upon using tropisetron.
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1421 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
Regulates outgrowth and stabilization of peripheral microtubules (MTs). Upon ERBB2 activation, the MEMO1-RHOA-DIAPH1 signaling pathway elicits the phosphorylation and thus the inhibition of GSK3B at cell membrane. This prevents the phosphorylation of APC and CLASP2, allowing its association with the cell membrane.
In turn, membrane-bound APC allows the localization of MACF1 to the cell membrane, which is required for microtubule capture and stabilization
ATC A04AA03
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)
Tropisetron
Additional database identifiers
ChemSpider
16736476
BindingDB
50108392
PDB
TKT
ZINC
ZINC000100019233
HUGO Gene Nomenclature Committee (HGNC)
HGNC:5297
GenAtlas
HTR3A
GeneCards
HTR3A
GenBank Gene Database
D49394
GenBank Protein Database
681914
Guide to Pharmacology
373
UniProt Accession
5HT3A_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3430
GenAtlas
ERBB2
GeneCards
ERBB2
GenBank Gene Database
M11767
GenBank Protein Database
553282
Guide to Pharmacology
2019
UniProt Accession
ERBB2_HUMAN
DrugBank citations
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Structured knowledge from the free knowledge base
Wikipedia article
chemical compound used to treat nausea and vomiting following chemotherapy
Read on WikipediaATC classifications (Wikidata)
Linked open data from Wikidata (Q29428), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.