Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Fosphenytoin sodium
Drug ID BADD_D00971
Description Fosphenytoin is a water-soluble phenytoin prodrug used only in hospitals for the treatment of epileptic seizures. It works by slowing down impulses in the brain that cause seizures. Its main mechanism is to block frequency-dependent, use-dependent and voltage-dependent neuronal sodium channels, and therefore limit repetitive firing of action potentials.
Indications and Usage For the control of generalized convulsive status epilepticus and prevention and treatment of seizures occurring during neurosurgery. It can also be substituted, short-term, for oral phenytoin.
Marketing Status Prescription; Discontinued
ATC Code N03AB05
DrugBank ID DB01320
KEGG ID D02096
MeSH ID C043114
PubChem ID 56338
TTD Drug ID D0J5YC
NDC Product Code 0641-6137; 29902-0023; 52952-005; 65162-998; 65162-999; 0143-9788; 0069-5474; 64679-729; 63323-403; 0143-9782; 67457-517; 0069-6001; 14998-0018; 0069-5471; 0641-6136; 64679-730; 72375-0005; 82019-0002; 67457-516; 62756-874; 62331-027
Synonyms fosphenytoin | 3-(hydroxymethyl)phenytoin phosphate ester | ACC 9653 | ACC-9653 | Prodilantin | fosphenytoin sodium | fosphenytoin, disodium salt | 3-(hydroxymethyl)phenytoin disodium phosphate | HMPDP | Cerebyx
Chemical Information
Molecular Formula C16H13N2Na2O6P
CAS Registry Number 92134-98-0
SMILES C1=CC=C(C=C1)C2(C(=O)N(C(=O)N2)COP(=O)([O-])[O-])C3=CC=CC=C3.[Na+].[Na+]
Chemical Structure
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Hypokalaemia14.05.03.002--
Hypokinesia17.01.02.009--Not Available
Hypophosphataemia14.04.03.001--
Hyporeflexia17.02.01.003--
Hypotension24.06.03.002--
Hypotonia15.05.04.008; 17.05.02.002--Not Available
Hypoxia22.02.02.003--
Ileus07.13.01.001--
Infection11.01.08.002--Not Available
Influenza11.05.03.001; 22.07.02.001--Not Available
Injection site haemorrhage08.02.03.005; 12.07.03.005; 24.07.01.010--Not Available
Injection site inflammation08.02.03.008; 12.07.03.009--Not Available
Injection site oedema08.02.03.024; 12.07.03.024--Not Available
Injection site pain08.02.03.010; 12.07.03.011--Not Available
Injection site reaction08.02.03.014; 12.07.03.015--
Injury12.01.08.004--Not Available
Insomnia17.15.03.002; 19.02.01.002--
Intracranial pressure increased17.07.02.002--Not Available
Ketosis14.01.01.001--Not Available
Leukocytosis01.02.01.002--
Leukopenia01.02.02.001--Not Available
Liver function test abnormal13.03.01.013--Not Available
Loss of consciousness17.02.04.004--Not Available
Lymphadenopathy01.09.01.002--Not Available
Malaise08.01.01.003--
Meningitis11.01.03.001; 17.06.03.001--
Mental disability26.01.01.001--Not Available
Migraine17.14.02.001; 24.03.05.003--Not Available
Mood swings19.04.03.001--Not Available
Muscle spasms15.05.03.004--
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