Indication
Tonic-clonic epilepsy
Tonic-clonic epilepsy refers to a central nervous system disorder characterized by recurrent tonic-clonic seizures, previously termed grand mal convulsions. Read more about Tonic-clonic epilepsy
298 drugs 125 manufacturers
Drugs that treat it
Common Tonic-clonic epilepsy therapies.
CARBAMAZEPINE
PRIMIDONE
PHENYTOIN SODIUM EXTENDED
CARBAMAZEPINE
CARBAMAZEPINE ER (carbamazepine)
LAMOTRIGINE
TOPIRAMATE
PHENYTOIN
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Coming soonTonic-clonic epilepsy refers to a central nervous system disorder characterized by recurrent tonic-clonic seizures, previously termed grand mal convulsions.
These seizures affect pediatric and adult populations and stem from abnormal, excessive, hypersynchronous neuronal discharges that rapidly engage bilateral cerebral hemispheres, either arising generalized from onset or evolving from a focal seizure focus.
Clinically, episodes are marked by sudden loss of consciousness, an initial tonic phase of generalized muscular rigidity, and a subsequent clonic phase featuring bilateral, rhythmic jerking of the extremities.
Episodes often involve autonomic instability, tongue biting, and urinary incontinence, typically concluding with an exhaustive postictal period of confusion, flaccidity, or coma.
- nih.gov
Tonic-clonic epilepsy refers to a central nervous system disorder characterized by recurrent tonic-clonic seizures, previously termed grand mal convulsions These seizures affect pediatric and adult populations and stem from abnormal, excessive, hypersynchronous neuronal discharges that rapidly engage bilateral cerebral hemispheres, either arising generalized from onset or evolving from a focal seizure focus Clinically, episodes are marked by sudden loss of consciousness, an initial tonic phase o...
- nih.gov
Tonic-clonic epilepsy refers to a central nervous system disorder characterized by recurrent tonic-clonic seizures, previously termed grand mal convulsions These seizures affect pediatric and adult populations and stem from abnormal, excessive, hypersynchronous neuronal discharges that rapidly engage bilateral cerebral hemispheres, either arising generalized from onset or evolving from a focal seizure focus
- nih.gov
These seizures affect pediatric and adult populations and stem from abnormal, excessive, hypersynchronous neuronal discharges that rapidly engage bilateral cerebral hemispheres, either arising generalized from onset or evolving from a focal seizure focus Clinically, episodes are marked by sudden loss of consciousness, an initial tonic phase of generalized muscular rigidity, and a subsequent clonic phase featuring bilateral, rhythmic jerking of the extremities
- nih.gov
Episodes often involve autonomic instability, tongue biting, and urinary incontinence, typically concluding with an exhaustive postictal period of confusion, flaccidity, or coma
- medlink.com
Episodes often involve autonomic instability, tongue biting, and urinary incontinence, typically concluding with an exhaustive postictal period of confusion, flaccidity, or coma
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