Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Acetazolamide sodium
Drug ID BADD_D00026
Description One of the carbonic anhydrase inhibitors that is sometimes effective against absence seizures. It is sometimes useful also as an adjunct in the treatment of tonic-clonic, myoclonic, and atonic seizures, particularly in women whose seizures occur or are exacerbated at specific times in the menstrual cycle. However, its usefulness is transient often because of rapid development of tolerance. Its antiepileptic effect may be due to its inhibitory effect on brain carbonic anhydrase, which leads to an increased transneuronal chloride gradient, increased chloride current, and increased inhibition. (From Smith and Reynard, Textbook of Pharmacology, 1991, p337)
Indications and Usage For adjunctive treatment of: edema due to congestive heart failure; drug-induced edema; centrencephalic epilepsies; chronic simple (open-angle) glaucoma
Marketing Status Prescription; Discontinued
ATC Code S01EC01
DrugBank ID DB00819
KEGG ID D01196
MeSH ID D000086
PubChem ID 13290219
TTD Drug ID D0E1SW
NDC Product Code 67457-853; 63552-116
Synonyms Acetazolamide | Acetazolam | Acetazolamide Sodium, (Sterile) | Acetazolamide, Monosodium Salt | Ak-Zol | Ak Zol | AkZol | Apo-Acetazolamide | Apo Acetazolamide | ApoAcetazolamide | Diacarb | Diamox | Diuramide | Défiltran | Edemox | Glauconox | Glaupax | Huma-Zolamide | Huma Zolamide | HumaZolamide | Acetadiazol
Chemical Information
Molecular Formula C4H5N4NaO3S2
CAS Registry Number 1424-27-7
SMILES CC(=O)NC1=NN=C(S1)S(=O)(=O)[NH-].[Na+]
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
AcidosisCarbonic anhydrase 12O43570T16987Not Available
AcidosisParathyroid hormone/parathyroid hormone-related peptide receptorQ03431T67710Not Available
Cardiovascular disorderCarbonic anhydrase 12O43570T16987Not Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Agranulocytosis01.02.03.001--Not Available
Aplastic anaemia01.03.03.002--Not Available
Confusional state17.02.03.005; 19.13.01.001--
Diarrhoea07.02.01.001--
Dysgeusia17.02.07.003; 07.14.03.001--
Electrolyte imbalance14.05.01.002--Not Available
Gastrointestinal disorder07.11.01.001--Not Available
Glycosuria20.02.01.005--
Haematuria20.02.01.006; 24.07.01.047--
Hepatic failure09.01.03.002--
Hepatic necrosis09.01.07.002--
Melaena24.07.02.013; 07.12.02.004--Not Available
Metabolic acidosis14.01.01.003--Not Available
Myopia06.02.04.002--Not Available
Nausea07.01.07.001--
Paraesthesia17.02.06.005--
Paralysis17.01.04.004--Not Available
Photosensitivity reaction23.03.09.003--
Polyuria20.02.03.002--Not Available
Seizure17.12.03.001--
Somnolence19.02.05.003; 17.02.04.006--
Stevens-Johnson syndrome10.01.03.020; 23.03.01.007; 12.03.01.014; 11.07.01.005--
Tinnitus17.04.07.004; 04.04.01.002--
Toxic epidermal necrolysis23.03.01.008; 12.03.01.015; 11.07.01.006; 10.01.01.006--
Urticaria23.04.02.001; 10.01.06.001--
Vomiting07.01.07.003--
Hypoacusis04.02.01.006--
Decreased appetite14.03.01.005; 08.01.09.028--
Blood disorder01.05.01.004--Not Available
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