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ANTICONVULSANT

The 'anticonvulsants', sometimes also called 'antiepileptics', belong to a diverse group of pharmaceuticals used in prevention of the occurrence of epileptic seizures. More and more, anticonvulsants are also finding ways into the treatment of bipolar disorder, since many seem to act as mood stabilizers. The goal of an anticonvulsant is to suppress the rapid and excessive firing of neurons that start a seizure. Failing this, a good anticonvulsant would prevent the spread of the seizure within the brain and offer protection against possible excitotoxic effects that may result in brain damage.
Many anticonvulsants block Sodium (Na+) channels, Calcium (Ca2+) channels, AMPA receptors or NMDA receptors. Some anticonvulsants inhibit the metabolism of GABA or increase its release.
In the following list, the dates in parentheses are the earliest approved use of the drug.

Contents
Aldehydes
Aromatic allylic alcohols
Barbiturates
Benzodiazepines
Bromides
Carbamates
Carboxamides
Fatty acids
Fructose derivatives
Gaba analogs
Hydantoins
Oxazolidinediones
Propionates
Pyrimidinediones
Pyrrolidines
Succinimides
Sulfonamides
Triazines
Ureas
Valproylamides (amide derivatives of valproate)
See also
References
External links

Aldehydes


''Main article: Aldehydes''

Paraldehyde (1882). One of the earliest anticonvulsants. Still used to treat status epilepticus, particularly where there are no resuscitation facilities.

Aromatic allylic alcohols



Stiripentol (2001 - limited availability). Indicated for the treatment of severe myoclonic epilepsy in infancy (SMEI).

Barbiturates


''Main article: Barbiturates''
Barbiturates are drugs that act as central nervous system (CNS) depressants, and by virtue of this they produce a wide spectrum of effects, from mild sedation to anesthesia. The following are classified as anticonvulsants:

Phenobarbital (1912). See also the related drug primidone.

Methylphenobarbital (1935). Known as mephobarbital in the US. No longer marketed in the UK

Metharbital (1952). No longer marketed in the UK or US.

Barbexaclone (1982). Only available in some European countries.
Phenobarbital was the main anticonvulsant from 1912 till the development of phenytoin in 1938. Today, phenobarbital is rarely used to treat epilepsy in new patients since there are other effective drugs that are less sedating. Phenobarbital sodium injection can be used to stop acute convulsions or status epilepticus, but a benzodiazepine such as lorazepam, diazepam or midazolam is usually tried first. Other barbiturates only have an anticonvulsant effect at anaesthetic doses.

Benzodiazepines


''Main article: Benzodiazepines''
The benzodiazepines are a class of drugs with hypnotic, anxiolytic, anticonvulsive, amnestic and muscle relaxant properties. The relative strength of each of these properties in any given benzodiazepine varies greatly and influences the indications for which it is prescribed. Long-term use can be problematic due to the development of tolerance and dependency. Of the many drugs in this class, only a few are used to treat epilepsy:

Clobazam (1979). Notably used on a short-term basis around menstruation in women with catamenial epilepsy.

Clonazepam (1974).

Clorazepate (1972).
The following benzodiazepines are used to treat status epilepticus:

Diazepam (1963). Can be given rectally by trained care-givers.

Midazolam (N/A). Increasingly being used as an alternative to diazepam. This water-soluble drug is squirted into the side of the mouth but not swallowed. It is rapidly absorbed by the buccal mucosa.

Lorazepam (1972). Given by injection in hospital.

Bromides


''Main article: Bromides''

Potassium bromide (1857). The earliest effective treatment for epilepsy. There would not be a better drug for epilepsy until phenobarbital in 1912. It is still used as an anticonvulsant for dogs and cats.

Carbamates


''Main article: Carbamates''

Felbamate (1993). This effective anticonvulsant has had its usage severely restricted due to rare but life-threatening side effects.

Carboxamides


''Main article: Carboxamides''
The following are carboxamides:

Carbamazepine (1965). A popular anticonvulsant that is available in generic formulations.

Oxcarbazepine (1990). A derivative of carbamazepine that has similar efficacy but is better tolerated.

Fatty acids


''Main article: Fatty acids''
The following are fatty-acids:

★ The valproatesvalproic acid, sodium valproate, and divalproex sodium (1978).

Vigabatrin (1989).

Progabide

Tiagabine (1997).
''Vigabatrin and progabide are also analogs of GABA.''

Fructose derivatives


''Main article: Fructose''

Topiramate (1995).

Gaba analogs



Gabapentin (1993).

Pregabalin (2004).

Hydantoins


''Main article: Hydantoins''
The following are hydantoins:

Ethotoin (1957).

Phenytoin (1938).

Mephenytoin

Fosphenytoin (1996).

Oxazolidinediones


''Main article: Oxazolidinediones''
The following are oxazolidinediones:

Paramethadione

Trimethadione (1946).

Ethadione

Propionates


''Main article: Propionates''

Beclamide

Pyrimidinediones


''Main article: Pyrimidinediones''

Primidone (1952).

Pyrrolidines


''Main article: Pyrrolidines''

Brivaracetam

Levetiracetam (1999).

Seletracetam

Succinimides


''Main article: Succinimides''
The following are succinimides:

Ethosuximide (1955).

Phensuximide

Mesuximide

Sulfonamides


''Main article: Sulfonamides''

Acetazolamide (1953).

Sulthiame

Methazolamide

Zonisamide (1990).

Triazines


''Main article: Triazines''

Lamotrigine (1991).

Ureas


''Main article: Ureas''

Pheneturide

Phenacemide

Valproylamides (amide derivatives of valproate)


''Main article: Amides''

Valpromide

Valnoctamide

See also



ATC code N03

References



Drug Reference for FDA Approved Epilepsy Drugs

UK Anti-Epileptic Drugs List

External links



eMedicine: Antiepileptic Drugs: an overview

NINDS: Anticonvulsant Screening Program

Use of Anticonvulsants in Pharmacotherapy of Bronchial Asthma

MDNG: Anticonvulsants and Bone Health

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