Drug class
Anticonvulsant - GABA Modulators
Anticonvulsant GABA modulators constitute a pharmacologic class of antiseizure medications that suppress central nervous system neuronal hyperexcitability by augmenting gamma-aminobutyric acid–mediated inhibitory signaling. Read more about Anticonvulsant - GABA Modulators
18 drugs in this class 17 manufacturers
Drugs in Anticonvulsant - GABA Modulators
SABRIL (vigabatrin)
TIAGABINE HCL
VIGABATRIN
VIGABATRIN
VIGABATRIN
VIGADRONE (vigabatrin)
VIGABATRIN
ZTALMY (ganaxolone)
Anticonvulsant GABA modulators constitute a pharmacologic class of antiseizure medications that suppress central nervous system neuronal hyperexcitability by augmenting gamma-aminobutyric acid–mediated inhibitory signaling.
These agents primarily function as positive allosteric modulators of postsynaptic GABAA receptors—increasing receptor affinity, opening frequency, or chloride channel open duration—or by elevating synaptic GABA levels through the inhibition of its reuptake or enzymatic degradation.
The resulting chloride influx hyperpolarizes the neuronal membrane, stabilizing the resting potential and dampening seizure propagation.
Clinically, medications within this class are utilized across diverse neurological indications, predominantly in the management of focal and generalized epilepsy, acute seizure clusters, and status epilepticus.
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nih.gov
Anticonvulsant GABA modulators constitute a pharmacologic class of antiseizure medications that suppress central nervous system neuronal hyperexcitability by augmenting gamma-aminobutyric acid–mediated inhibitory signaling
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epilepsysociety.org.uk
Anticonvulsant GABA modulators constitute a pharmacologic class of antiseizure medications that suppress central nervous system neuronal hyperexcitability by augmenting gamma-aminobutyric acid–mediated inhibitory signaling
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drugbank.com
These agents primarily function as positive allosteric modulators of postsynaptic GABAA receptors—increasing receptor affinity, opening frequency, or chloride channel open duration—or by elevating synaptic GABA levels through the inhibition of its reuptake or enzymatic degradation The resulting chloride influx hyperpolarizes the neuronal membrane, stabilizing the resting potential and dampening seizure propagation
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nih.gov
These agents primarily function as positive allosteric modulators of postsynaptic GABAA receptors—increasing receptor affinity, opening frequency, or chloride channel open duration—or by elevating synaptic GABA levels through the inhibition of its reuptake or enzymatic degradation
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patsnap.com
These agents primarily function as positive allosteric modulators of postsynaptic GABAA receptors—increasing receptor affinity, opening frequency, or chloride channel open duration—or by elevating synaptic GABA levels through the inhibition of its reuptake or enzymatic degradation The resulting chloride influx hyperpolarizes the neuronal membrane, stabilizing the resting potential and dampening seizure propagation
-
nih.gov
These agents primarily function as positive allosteric modulators of postsynaptic GABAA receptors—increasing receptor affinity, opening frequency, or chloride channel open duration—or by elevating synaptic GABA levels through the inhibition of its reuptake or enzymatic degradation Clinically, medications within this class are utilized across diverse neurological indications, predominantly in the management of focal and generalized epilepsy, acute seizure clusters, and status epilepticus
-
nih.gov
Clinically, medications within this class are utilized across diverse neurological indications, predominantly in the management of focal and generalized epilepsy, acute seizure clusters, and status epilepticus
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