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Pancuronium
Pavulon (pancuronium) is a small molecule pharmaceutical. Pancuronium was first approved as Pavulon on 1982-01-01. The pharmaceutical is active against acetylcholine receptor subunit alpha.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Pancuronium bromide
Tradename
Company
Number
Date
Products
PAVULONOrganonN-017015 DISCN1982-01-01
2 products, RLD
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Labels
FDA
EMA
Brand Name
Status
Last Update
pancuronium bromideANDA2019-01-31
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
M: Musculo-skeletal system drugs
M03: Muscle relaxants
M03A: Muscle relaxants, peripherally acting agents
M03AC: Other quaternary ammonium compounds in atc, muscle relaxants, peripherally acting
M03AC01: Pancuronium
HCPCS
No data
Clinical
Clinical Trials
35 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Breast neoplasmsD001943EFO_0003869C50235
Metabolic bone diseasesD001851HP_00009381315
OsteoporosisD010024EFO_0003882M81.012114
Osteogenesis imperfectaD010013Q78.01113
NeoplasmsD009369C80112
Neoplasm metastasisD009362EFO_000970822
Prostatic neoplasmsD011471C6111
Bone diseasesD001847M89.911
Chronic kidney disease-mineral and bone disorderD012080EFO_1001152N25.011
Osteitis deformansD010001EFO_0004261M8811
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple myelomaD009101C90.01214
Plasma cell neoplasmsD0542191213
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Low back painD017116HP_0003419M54.5223
PainD010146EFO_0003843R521112
Drug therapyD00435811
Magnetic resonance imagingD00827911
Back painD001416HP_0003418M5411
Intervertebral disc degenerationD055959HP_000841911
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Acquired hyperostosis syndromeD020083EFO_100116411
ArthroplastyD00117811
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Bone densityD015519EFO_0003923M8511
Femur head necrosisD00527111
Cerebral palsyD002547G8011
Spinal dysraphismD016135EFO_1001210Q0511
Heterotopic ossificationD00999911
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common namePANCURONIUM
INNpancuronium bromide
Description
Pancuronium bromide is a bromide salt consisting of two bromide ions and one pancuronium dication. It has a role as a muscle relaxant, a cholinergic antagonist and a nicotinic antagonist. It contains a pancuronium.
Classification
Small molecule
Drug classquaternary ammonium derivatives: neuromuscular blocking agents; quaternary ammonium derivatives: neuromuscular blocking agents
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@@]4(C)[C@H]3C[C@H]([N+]3(C)CCCCC3)[C@@H]4OC(C)=O)[C@@]2(C)C[C@@H]1[N+]1(C)CCCCC1
Identifiers
PDB
CAS-ID15500-66-0
RxCUI7884
ChEMBL IDCHEMBL185073
ChEBI ID7907
PubChem CID27350
DrugBankDB01337
UNII IDU9LY9Y75X2 (ChemIDplus, GSRS)
Target
Agency Approved
CHRNA1
CHRNA1
Organism
Homo sapiens
Gene name
CHRNA1
Gene synonyms
ACHRA, CHNRA
NCBI Gene ID
Protein name
acetylcholine receptor subunit alpha
Protein synonyms
acetylcholine receptor, nicotinic, alpha 1 (muscle), cholinergic receptor, nicotinic alpha 1, cholinergic receptor, nicotinic, alpha 1 (muscle), cholinergic receptor, nicotinic, alpha polypeptide 1 (muscle), muscle nicotinic acetylcholine receptor, nicotinic acetylcholine receptor alpha subunit, nicotinic cholinergic receptor alpha 1
Uniprot ID
Mouse ortholog
Chrna1 (11435)
acetylcholine receptor subunit alpha (P04756)
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 5,701 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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13,541 adverse events reported
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