| ADR Ontology |
| ADR Term |
Juvenile myoclonic epilepsy |
| ADR ID |
BADD_A10262 |
| ADR Hierarchy |
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| Description |
A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323) [MeSH] |
| MedDRA Code |
10071082 |
| MeSH ID |
D020190
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ADR Severity Grade (FAERS)
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ADR Severity Grade (CTCAE)
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Not Available
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| Synonym |
| Juvenile myoclonic epilepsy | Myoclonic Epilepsy, Juvenile | Epilepsy, Juvenile Myoclonic | Epilepsy, Myoclonic Juvenile | Juvenile Epilepsy, Myoclonic | Myoclonic Juvenile Epilepsy | JME (Juvenile Myoclonic Epilepsy) | JMEs (Juvenile Myoclonic Epilepsy) | Epilepsy, Myoclonic, Juvenile | Juvenile Myoclonic Epilepsy | Juvenile Myoclonic Epilepsy of Janz | Janz Syndrome | Petit Mal, Impulsive, Janz | Janz Juvenile Myoclonic Epilepsy | Impulsive Petit Mal, Janz | Janz Impulsive Petit Mal | Impulsive Petit Mal Epilepsy | Petit Mal, Impulsive | Myoclonic Epilepsy, Juvenile, 1 | Myoclonic Epilepsy, Adolescent | Epilepsy, Adolescent Myoclonic | Adolescent Myoclonic Epilepsy |
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| Drugs Leading to the ADR |
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