Adverse Drug Reaction Classification System

         

Pharmaceutical Information
Drug Name Methylscopolamine bromide
Drug ID BADD_D01437
Description A muscarinic antagonist used to study binding characteristics of muscarinic cholinergic receptors.
Indications and Usage Used as adjunctive therapy for the treatment of peptic ulcer. Also used to treat nausea and vomiting due to motion sickness.
Marketing Status approved
ATC Code Not Available
DrugBank ID DB00462
KEGG ID D00715
MeSH ID D019832
PubChem ID 23724781
TTD Drug ID Not Available
NDC Product Code 55742-014; 76385-100; 51991-191; 43063-741; 76385-101; 51927-0047; 43063-740; 51991-192
UNII VDR09VTQ8U
Synonyms N-Methylscopolamine | N Methylscopolamine | Methscopolamine | N-Methylscine Methylsulfate | Methylsulfate, N-Methylscine | N Methylscine Methylsulfate | N-Methylscopolamine Bromide | Bromide, N-Methylscopolamine | N Methylscopolamine Bromide | Hyoscine Methobromide | Methobromide, Hyoscine | Scopolamine Methylbromide | Methylbromide, Scopolamine | N-Methylscopolamine Iodide | Iodide, N-Methylscopolamine | N Methylscopolamine Iodide | Hyoscine Methiodide | Methiodide, Hyoscine | N-Methylscopolamine Methylsulfate | Methylsulfate, N-Methylscopolamine | N Methylscopolamine Methylsulfate | Methylscopolammonium Methylsulfate | Methylsulfate, Methylscopolammonium | N-Methylscopolamine Nitrate | N Methylscopolamine Nitrate | Nitrate, N-Methylscopolamine | Methylscopolamine Nitrate | Nitrate, Methylscopolamine | Skopyl | Ulix | DD-234 | DD 234 | DD234 | N-Methylscopolamine Methylchloride | Methylchloride, N-Methylscopolamine | N Methylscopolamine Methylchloride
Chemical Information
Molecular Formula C18H24BrNO4
CAS Registry Number 155-41-9
SMILES C[N+]1(C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4)C.[Br-]
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 distension07.01.04.001--
Accommodation disorder06.02.04.001---
Ageusia07.14.03.003; 17.02.07.001---
Anaphylactic reaction10.01.07.001; 24.06.03.006--
Anaphylactic shock10.01.07.002; 24.06.02.004---
Asthenia08.01.01.001---
Confusional state17.02.03.005; 19.13.01.001--
Constipation07.02.02.001--
Cycloplegia06.05.03.002; 17.17.02.003---
Dermatitis allergic10.01.03.014; 23.03.04.003---
Dizziness02.11.04.006; 17.02.05.003; 24.06.02.007--
Dry mouth07.06.01.002--
Feeling abnormal08.01.09.014---
Headache17.14.01.001--
Hypersensitivity10.01.03.003--
Hypohidrosis08.01.03.029; 23.02.03.005--
Insomnia17.15.03.002; 19.02.01.002--
Intraocular pressure increased13.07.04.002---
Mydriasis06.05.03.004; 17.02.11.003---
Nausea07.01.07.001--
Nervousness19.06.02.003---
Palpitations02.11.04.012--
Somnolence17.02.04.006; 19.02.05.003--
Tachycardia02.03.02.007---
Tension19.06.02.005---
Urinary hesitation20.02.02.009---
Urinary retention20.02.02.011--
Urticaria10.01.06.001; 23.04.02.001--
Vision blurred06.02.06.007; 17.17.01.010--
Vomiting07.01.07.003--
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