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Drug ReportsOtilonium bromide
Otilonium bromide
Otilonium bromide is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Trade Name
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New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
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Agency Specific
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ATC Codes
A: Alimentary tract and metabolism drugs
A03: Drugs for functional gastrointestinal disorders
A03A: Drugs for functional gastrointestinal disorders
A03AB: Synthetic anticholinergics, quaternary ammonium compounds for functional gastrointestinal disorders
A03AB06: Otilonium bromide
A03C: Antispasmodics in combination with psycholeptics
A03CA: Synthetic anticholinergic agents in combination with psycholeptics
A03CA04: Otilonium bromide and psycholeptics
HCPCS
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Clinical
Clinical Trials
4 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Irritable bowel syndromeD043183EFO_0000555K58213
SyndromeD013577213
GastroscopyD00577311
Indications Phases 3
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Indications Phases 2
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameOtilonium bromide
INNotilonium bromide
Description
Otilonium bromide, sold under the trade name Spasmomen among others, is an antimuscarinic and calcium channel blocker used to relieve spasmodic pain of the gut, especially in irritable bowel syndrome. This means it works in the gut themselves, by relaxing the small muscles of the intestines, which results in relieving cramps and therefore reduces pain.
Classification
Small molecule
Drug classquaternary ammonium derivatives; quaternary ammonium derivatives
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Structure (InChI/SMILES or Protein Sequence)
CCCCCCCCOc1ccccc1C(=O)Nc1ccc(C(=O)OCC[N+](C)(CC)CC)cc1.[Br-]
Identifiers
PDB
CAS-ID26095-59-0
RxCUI
ChEMBL IDCHEMBL2103773
ChEBI ID
PubChem CID72092
DrugBank
UNII ID21HN3N72PV (ChemIDplus, GSRS)
Target
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Variants
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Safety
Black-box Warning
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Adverse Events
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33 adverse events reported
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