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Anticonvulsant

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Anticonvulsant
Drug class
Class identifiers
SynonymsAntiepileptic drugs, antiseizure drugs
UseEpilepsy
ATC codeN03
Biological targetBrain
Legal status
In Wikidata

Anticonvulsants (also known as antiepileptic drugs, antiseizure drugs, or anti-seizure medications (ASM)) are a diverse group of pharmacological agents used in the treatment of epileptic seizures.[1] Anticonvulsants are also increasingly being used in the treatment of bipolar disorder[2][3] and borderline personality disorder,[4] since many seem to act as mood stabilizers, and for the treatment of neuropathic pain.[5] Anticonvulsants suppress the excessive rapid firing of neurons during seizures.[6] Anticonvulsants also prevent the spread of the seizure within the brain.[7]

Conventional antiepileptic drugs may block sodium channels or enhance γ-aminobutyric acid (GABA) function. Several antiepileptic drugs have multiple or uncertain mechanisms of action.[8] Next to the voltage-gated sodium channels and components of the GABA system, their targets include GABAA receptors, the GABA transporter type 1, and GABA transaminase.[9] Additional targets include voltage-gated calcium channels, SV2A, and α2δ.[10][11] By blocking sodium or calcium channels, antiepileptic drugs reduce the release of excitatory glutamate, whose release is considered to be elevated in epilepsy, but also that of GABA.[12] This is probably a side effect or even the actual mechanism of action for some antiepileptic drugs, since GABA can itself, directly or indirectly, act proconvulsively.[12] Another potential target of antiepileptic drugs is the peroxisome proliferator-activated receptor alpha.[13][14][15][16][17][18][19]

Some anticonvulsants have shown antiepileptogenic effects in animal models of epilepsy.[20] That is, they either prevent the development of epilepsy or can halt or reverse the progression of epilepsy. However, no drug has been shown in human trials to prevent epileptogenesis (the development of epilepsy in an individual at risk, such as after a head injury).[21]

Terminology

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Anticonvulsants are more accurately called antiepileptic drugs (AEDs) because not every epileptic seizure involves convulsion, and vice versa, not every convulsion is caused by an epileptic seizure.[22] They are also often referred to as antiseizure drugs because they provide symptomatic treatment only and have not been demonstrated to alter the course of epilepsy.[23]

Approval

[edit]

The usual method of achieving approval for a drug is to show it is effective when compared against placebo, or that it is more effective than an existing drug. In monotherapy (where only one drug is taken) it is considered unethical by most to conduct a trial with placebo on a new drug of uncertain efficacy. This is because untreated epilepsy leaves the patient at significant risk of death. Therefore, almost all new epilepsy drugs are initially approved only as adjunctive (add-on) therapies. Patients whose epilepsy is uncontrolled by their medication (i.e., it is refractory to treatment) are selected to see if supplementing the medication with the new drug leads to an improvement in seizure control. Any reduction in the frequency of seizures is compared against a placebo.[21] The lack of superiority over existing treatment, combined with lacking placebo-controlled trials, means that few modern drugs have earned FDA approval as initial monotherapy. In contrast, Europe only requires equivalence to existing treatments and has approved many more. Despite their lack of FDA approval, the American Academy of Neurology and the American Epilepsy Society still recommend a number of these new drugs as initial monotherapy.[21]

Drugs

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In the following list, the dates in parentheses are the earliest approved use of the drug.

Aldehydes

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Main article: Aldehyde

Aromatic allylic alcohols

[edit]

Barbiturates

[edit]
Main article: Barbiturate

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:[30]

Benzodiazepines

[edit]
Main article: Benzodiazepine

The benzodiazepines are a class of drugs with hypnotic, anxiolytic, anticonvulsive, amnestic and muscle relaxant properties. Benzodiazepines act as a central nervous system depressant. 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 to the anticonvulsant effects and dependency.[31][32][33][34] Of many drugs in this class, only a few are used to treat epilepsy:

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.

Nitrazepam, temazepam, and especially nimetazepam are powerful anticonvulsant agents, however their use is rare due to an increased incidence of side effects and strong sedative and motor-impairing properties.

Bromides

[edit]
Main article: Bromide
  • Potassium bromide (1857). The earliest effective treatment for epilepsy. There would not be a better drug until phenobarbital in 1912. It is still used as an anticonvulsant for dogs and cats but is no longer used in humans.

Carbamates

[edit]
Main article: Carbamate
  • Felbamate (1993). This effective anticonvulsant has had its usage severely restricted due to rare but life-threatening side effects.[35][36][37]
  • Cenobamate (2019).

Carboxamides

[edit]
Carbamazepine
Main article: Carboxamide

The following are carboxamides:

  • Carbamazepine (1963). A popular anticonvulsant that is available in generic formulations.
  • Oxcarbazepine (1990). A derivative of carbamazepine that has similar efficacy and is better tolerated and is also available generically.
  • Eslicarbazepine acetate (2009).
  • Photoswitchable analogues of carbamazepine (2024) are research compounds developed to control its pharmacological activity locally and on demand using light, with the purpose to reduce adverse systemic effects.[38] One of these compounds (carbadiazocine, based on a bridged azobenzene) has been shown to produce analgesia with noninvasive illumination in a rat model of neuropathic pain.

Fatty acids

[edit]
Main article: Fatty acid

The following are fatty-acids:

Vigabatrin and progabide are also analogs of GABA.

Fructose derivatives

[edit]
Main article: Fructose

Gabapentinoids

[edit]
Main article: Gabapentinoid
GABA analogues
GABA analogues
Binding sites of pregabalin and the non-gabapentenoid ziconotide to the voltage-gated calcium channel complex.
Voltage-gated calcium channel

Gabapentinoids are used in epilepsy, neuropathic pain, fibromyalgia, restless leg syndrome, opioid withdrawal and generalized anxiety disorder (GAD). Gabapentinoids block voltage-gated calcium channels, mainly the N-Type, and P/Q-type calcium channels. The following are gabapentinoids:

Gabapentinoids are analogs of GABA, but they do not act on GABA receptors. They have analgesic, anticonvulsant, and anxiolytic effects.

Hydantoins

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Main article: Hydantoin

The following are hydantoins:

Oxazolidinediones

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Main article: 2,4-Oxazolidinedione

The following are oxazolidinediones:

Propionates

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Main article: Propionate

Pyrimidinediones

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Main article: Pyrimidinedione

Pyrrolidines

[edit]
Main article: Pyrrolidine

Succinimides

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Main article: Succinimide

The following are succinimides:

Sulfonamides

[edit]
Main article: Sulfonamide (medicine)

Triazines

[edit]
Main article: Triazine

Ureas

[edit]
Main article: Urea

Valproylamides

[edit]
Main article: Amide

Other

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Non-pharmaceutical anticonvulsants

[edit]
Further information: Epilepsy § Management

The ketogenic diet and vagus nerve stimulation are alternative treatments for epilepsy without the involvement of pharmaceuticals. The ketogenic diet consists of a high-fat, low-carbohydrate diet, and has shown good results in patients whose epilepsy has not responded to medications and who cannot receive surgery. The vagus nerve stimulator is a device that can be implanted into patients with epilepsy, especially that which originates from a specific part of the brain. However, both of these treatment options can cause severe adverse effects. Additionally, while seizure frequency typically decreases, they often do not stop entirely.[39][40]

Treatment guidelines

[edit]

According to guidelines by the American Academy of Neurology and American Epilepsy Society,[41] mainly based on a major article review in 2004,[42] patients with newly diagnosed epilepsy who require treatment can be initiated on standard anticonvulsants such as carbamazepine, phenytoin, valproic acid/valproate semisodium, phenobarbital, or on the newer anticonvulsants gabapentin, lamotrigine, oxcarbazepine or topiramate. The choice of anticonvulsants depends on individual patient characteristics.[41] Both newer and older drugs are generally equally effective in new onset epilepsy.[41] The newer drugs tend to have fewer side effects.[41] For newly diagnosed partial or mixed seizures, there is evidence for using gabapentin, lamotrigine, oxcarbazepine or topiramate as monotherapy.[41] Lamotrigine can be included in the options for children with newly diagnosed absence seizures.[41]

History

[edit]

The first anticonvulsant was bromide, suggested in 1857 by the British gynecologist Charles Locock who used it to treat women with "hysterical epilepsy" (probably catamenial epilepsy). Bromides are effective against epilepsy, and also cause impotence, which is not related to its anti-epileptic effects. Bromide also suffered from the way it affected behaviour, introducing the idea of the "epileptic personality" which was actually a result of medication. Phenobarbital was first used in 1912 for both its sedative and antiepileptic properties. By the 1930s, the development of animal models in epilepsy research led to the development of phenytoin by Tracy Putnam and H. Houston Merritt, which had the distinct advantage of treating epileptic seizures with less sedation.[43] By the 1970s, a National Institutes of Health initiative, the Anticonvulsant Screening Program, headed by J. Kiffin Penry, served as a mechanism for drawing the interest and abilities of pharmaceutical companies in the development of new anticonvulsant medications.

Marketing approval history

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The following table lists anticonvulsant drugs together with the date their marketing was approved in the US, UK and France. Data for the UK and France are incomplete. The European Medicines Agency approves drugs throughout the European Union. Some of the drugs are no longer marketed.

Drug Brand US UK France
acetazolamide Diamox 1953-07-2727 July 1953[44] 1988[45]
brivaracetam Briviact 2016-02-1818 February 2016[46][47]
carbamazepine Tegretol 1974-07-1515 July 1974[48][49] 1965[45] 1963[50]
cenobamate Xcopri 2019-11-2121 November 2019
clobazam Onfi/Frisium 2011-10-2121 October 2011[51][52] 1979[45]
clonazepam Klonopin/Rivotril 1975-06-044 June 1975[53] 1974[45]
diazepam Valium 1963-11-1515 November 1963[54]
divalproex sodium Depakote 1983-03-1010 March 1983[55]
eslicarbazepine Aptiom 2013-08-1111 August 2013[56][57]
ethosuximide Zarontin 1960-11-022 November 1960[58] 1955[45] 1962[50]
ethotoin Peganone 1957-04-2222 April 1957[59]
everolimus Afinitor/Votubia 2009-03-3030 January 2009[60]
felbamate Felbatol 1993-07-2929 July 1993[61]
fosphenytoin Cerebyx 1996-08-055 August 1996[62]
gabapentin Neurontin 1993-12-3030 December 1993[63] 1993-05May 1993[45][50] 1994-10October 1994[50]
lacosamide Vimpat 2008-10-2828 October 2008[64]
lamotrigine Lamictal 1994-12-2727 December 1994[65] 1991-10October 1991[45][50] 1995-05May 1995[50]
levetiracetam Keppra 1999-11-3030 November 1999[66] 2000-09-2929 September 2000[45][67] 2000-09-2929 September 2000[67]
mephenytoin Mesantoin 1946-10-2323 October 1946[68]
metharbital Gemonil 1952[69][70]
methsuximide Celontin 1957-02-088 February 1957[71]
methazolamide Neptazane 1959-01-2626 January 1959[72]
oxcarbazepine Trileptal 2000-01-1414 January 2000[73] 2000[45]
phenobarbital Luminal Unknown 1912[45] 1920[50]
phenytoin Dilantin/Epanutin 1938[50][74] 1938[45] 1941[50]
piracetam Nootropil never approved
phensuximide Milontin 1953[75][76]
pregabalin Lyrica 2004-12-3030 December 2004[77] 2004-07-066 July 2004[45][78] 2004-07-066 July 2004[78]
primidone Mysoline 1954-03-088 March 1954[79] 1952[45] 1953[50]
rufinamide Banzel/Inovelon 2008-11-1414 November 2008[80][81]
sodium valproate Epilim Unknown 1977-12December 1977[50] 1967-06June 1967[50]
stiripentol Diacomit 2018-08-2020 August 2018[82][83] 2007-01January 2007[28] 2007-01January 2007[28]
tiagabine Gabitril 1997-09-3030 September 1997[84][85] 1998[45] 1997-11November 1997[50]
topiramate Topamax 1996-12-2424 December 1996[86] 1995[45]
trimethadione Tridione 1946-01-2525 January 1946[87]
valproic acid Depakene/Convulex 1978-02-2828 February 1978[88] 1993[45]
vigabatrin Sabril 2009-08-2121 August 2009[89] 1989[45]
zonisamide Zonegran 2000-03-2727 March 2000[90] 2005-03-1010 March 2005[45][91] 2005-03-1010 March 2005[91]

Pregnancy

[edit]
See also: Epilepsy and pregnancy

Many of the commonly used anticonvulsant/anti-seizure medications (ASMs), such as valproate, phenytoin, carbamazepine, phenobarbitol, gabapentin have been reported to cause an increased risk of birth defects including major congenital malformations such as neural tube defects.[92] The risk of birth defects associated with taking these medications while pregnant may be dependent on the dose and on the timing of gestation (how well developed the baby is).[92] While trying to conceive a child and during pregnancy, medical advice should be followed to optimize the management of the person's epilepsy in order to keep the person and the unborn baby safe from epileptic seizures and also ensure that the risk of birth defects due to in utero exposure of anticonvulsants is as low as possible. Use of anticonvulsant medications should be carefully monitored during use in pregnancy.[93] For example, since the first trimester is the most susceptible period for fetal development, planning a routine antiepileptic drug dose that is safer for the first trimester could be beneficial to prevent pregnancy complications.[94]

Valproic acid, and its derivatives such as sodium valproate and divalproex sodium, causes cognitive deficit in the child, with an increased dose causing decreased intelligence quotient and use is associated with adverse neurodevelopmental outcomes (cognitive and behavioral)  in children.[95][96] On the other hand, evidence is conflicting for carbamazepine regarding any increased risk of congenital physical anomalies or neurodevelopmental disorders by intrauterine exposure.[95] Similarly, children exposed lamotrigine or phenytoin in the womb do not seem to differ in their skills compared to those who were exposed to carbamazepine.[95]

There is inadequate evidence to determine if newborns of women with epilepsy taking anticonvulsants have a substantially increased risk of hemorrhagic disease of the newborn.[93]

There is little evidence to suggest that anticonvulsant/ASM exposure through breastmilk has clinical effects on newborns. The Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) study showed that most blood concentrations in breastfed infants of mothers taking carbamazepine, oxcarbazepine, valproate, levetiracetam, and topiramate were quite low, especially in relationship to the mother's level and what the fetal level would have been during pregnancy. (Note: valproic acid is NOT a recommended ASM for people with epilepsy who are considering having children.) [97]

Infant exposure to newer ASMs (cenobamate, perampanel, brivaracetam, eslicarbazepine, rufinamide, levetiracetam, topiramate, gabapentin, oxcarbazepine, lamotrigine, and vigabatrin) via breastmilk was not associated with negative neurodevelopment (such as lower IQ and autism spectrum disorder) at 36 months.[98]

Several studies that followed children exposed to ASMs during pregnancy showed that a number of widely used ones (including lamotrigine and levetiracetam) carried a low risk of adverse neurodevelopmental outcomes (cognitive and behavioral) in children when compared to children born to mothers without epilepsy and children born to mothers taking other anti-seizure medications. Data from several pregnancy registries showed that children exposed to levetiracetam or lamotrigine during pregnancy had the lowest risk of developing major congenital malformations compared to those exposed to other ASMs. The risk of major congenital malformations for children exposed to these ASMs were within the range for children who were not exposed to any ASMs during pregnancy.[99]

People with epilepsy can have healthy pregnancies and healthy babies. However, proper planning and care is essential to minimize the risk of congenital malformations or adverse neurocognitive outcomes for the fetus while maintaining seizure control for the pregnant person with epilepsy. If possible, when planning pregnancy, people with epilepsy should switch to ASMs with the lowest teratogenic risk for major congenital malformations as well as the least risk of adverse neurodevelopmental outcomes (e.g., lower IQ or autism spectrum disorder). They should also work with their healthcare providers to identify the lowest effective ASM dosage that will maintain their seizure control while regularly checking medication levels throughout pregnancy.[100]

Data from studies conducted on women taking antiepileptic drugs for non-epileptic reasons, including depression and bipolar disorder, show that if high doses of the drugs are taken during the first trimester of pregnancy then there is the potential of an increased risk of congenital malformations.[101]

Research

[edit]

The mechanism of how anticonvulsants cause birth defects is not entirely clear. During pregnancy, the metabolism of many anticonvulsants is affected. There may be an increase in the clearance and resultant decrease in the blood concentration of lamotrigine, phenytoin, and to a lesser extent carbamazepine, and possibly decreases the level of levetiracetam and the active oxcarbazepine metabolite, the monohydroxy derivative.[93] In animal models, several anticonvulsant drugs have been demonstrated to induce neuronal apoptosis in the developing brain.[102][103][104][105][106]

References

[edit]
  1. ^ Al-Otaibi F (1 September 2019). "An overview of structurally diversified anticonvulsant agents". Acta Pharmaceutica (Zagreb, Croatia). 69 (3). Walter de Gruyter GmbH: 321–344. doi:10.2478/acph-2019-0023. ISSN 1846-9558. PMID 31259739.
  2. ^ Joshi A, Bow A, Agius M (2019). "Pharmacological Therapies in Bipolar Disorder: a Review of Current Treatment Options". Psychiatria Danubina. 31 (Suppl 3): 595–603. ISSN 0353-5053. PMID 31488797.
  3. ^ Keck PE Jr, McElroy SL, Strakowski SM (1998). "Anticonvulsants and antipsychotics in the treatment of bipolar disorder". The Journal of Clinical Psychiatry. 59 (Suppl 6): 74–82. PMID 9674940.
  4. ^ American Psychiatric Association, and American Psychiatric Association. Work Group on Borderline Personality Disorder. Practice guideline for the treatment of patients with borderline personality disorder. American Psychiatric Pub, 2001.
  5. ^ Rogawski MA, Löscher W (2004). "The neurobiology of antiepileptic drugs". Nature Reviews Neuroscience. 5 (7): 553–564. doi:10.1038/nrn1430. PMID 15208697. S2CID 2201038. Archived from the original on 16 December 2020. Retrieved 20 September 2020.
  6. ^ McLean MJ, Macdonald RL (June 1986). "Sodium valproate, but not ethosuximide, produces use- and voltage-dependent limitation of high frequency repetitive firing of action potentials of mouse central neurons in cell culture". Journal of Pharmacology and Experimental Therapeutics. 237 (3): 1001–1011. PMID 3086538.
  7. ^ Harden CL (1 May 1994). "New antiepileptic drugs". Neurology. 44 (5): 787–95. doi:10.1212/WNL.44.5.787. PMID 8190276. S2CID 75925846.
  8. ^ "Archived copy" (PDF). Archived from the original (PDF) on 3 November 2013. Retrieved 28 January 2013.{{cite web}}: CS1 maint: archived copy as title (link)
  9. ^ Rogawski MA, Löscher W (July 2004). "The neurobiology of antiepileptic drugs". Nature Reviews Neuroscience. 5 (7): 553–64. doi:10.1038/nrn1430. PMID 15208697. S2CID 2201038. Archived from the original on 16 December 2020. Retrieved 20 September 2020.
  10. ^ Rogawski MA, Bazil CW (July 2008). "New molecular targets for antiepileptic drugs: alpha(2)delta, SV2A, and K(v)7/KCNQ/M potassium channels". Curr Neurol Neurosci Rep. 8 (4): 345–52. doi:10.1007/s11910-008-0053-7. PMC 2587091. PMID 18590620.
  11. ^ Meldrum BS, Rogawski MA (January 2007). "Molecular targets for antiepileptic drug development". Neurotherapeutics. 4 (1): 18–61. doi:10.1016/j.nurt.2006.11.010. PMC 1852436. PMID 17199015.
  12. ^ a b Kammerer M, Rassner, M. P., Freiman, T. M., Feuerstein, T. J. (2 May 2011). "Effects of antiepileptic drugs on GABA release from rat and human neocortical synaptosomes". Naunyn-Schmiedeberg's Archives of Pharmacology. 384 (1): 47–57. doi:10.1007/s00210-011-0636-8. PMID 21533993. S2CID 1388805.
  13. ^ Puligheddu M, Pillolla G, Melis M, Lecca S, Marrosu F, De Montis MG, et al. (2013). Charpier S (ed.). "PPAR-alpha agonists as novel antiepileptic drugs: preclinical findings". PLOS ONE. 8 (5): e64541. Bibcode:2013PLoSO...864541P. doi:10.1371/journal.pone.0064541. PMC 3664607. PMID 23724059.
  14. ^ Citraro R, et al. (2013). "Antiepileptic action of N-palmitoylethanolamine through CB1 and PPAR-α receptor activation in a genetic model of absence epilepsy". Neuropharmacology. 69: 115–26. doi:10.1016/j.neuropharm.2012.11.017. PMID 23206503. S2CID 27701532.
  15. ^ Porta, N., Vallée, L., Lecointe, C., Bouchaert, E., Staels, B., Bordet, R., Auvin, S. (2009). "Fenofibrate, a peroxisome proliferator-activated receptor-alpha agonist, exerts anticonvulsive properties". Epilepsia. 50 (4): 943–8. doi:10.1111/j.1528-1167.2008.01901.x. PMID 19054409. S2CID 6796135.
  16. ^ Lampen A, Carlberg C, Nau H (2001). "Peroxisome proliferator-activated receptor delta is a specific sensor for teratogenic valproic acid derivatives". Eur J Pharmacol. 431 (1): 25–33. doi:10.1016/S0014-2999(01)01423-6. PMID 11716839.
  17. ^ Maguire JH, Murthy AR, Hall IH (1985). "Hypolipidemic activity of antiepileptic 5-phenylhydantoins in mice". Eur J Pharmacol. 117 (1): 135–8. doi:10.1016/0014-2999(85)90483-2. PMID 4085542.
  18. ^ Hall IH, Patrick MA, Maguire JH (1990). "Hypolipidemic activity in rodents of phenobarbital and related derivatives". Archiv der Pharmazie. 323 (9): 579–86. doi:10.1002/ardp.19903230905. PMID 2288480. S2CID 46002731.
  19. ^ Frigerio F, Chaffard G, Berwaer M, Maechler P (2006). "The antiepileptic drug topiramate preserves metabolism-secretion coupling in insulin secreting cells chronically exposed to the fatty acid oleate". Biochem Pharmacol. 72 (8): 965–73. doi:10.1016/j.bcp.2006.07.013. PMID 16934763.
  20. ^ Kaminski RM, Rogawski MA, Klitgaard H (2014). "The potential of antiseizure drugs and agents that act on novel molecular targets as antiepileptogenic treatments". Neurotherapeutics. 11 (2): 385–400. doi:10.1007/s13311-014-0266-1. PMC 3996125. PMID 24671870.
  21. ^ a b c Abou-Khalil BW (2007). "Comparative Monotherapy Trials and the Clinical Treatment of Epilepsy". Epilepsy Currents. 7 (5): 127–9. doi:10.1111/j.1535-7511.2007.00198.x. PMC 2043140. PMID 17998971.
  22. ^ "Antiseizure medication". Cleveland Clinic. Archived from the original on 16 March 2024. Retrieved 16 March 2024.
  23. ^ Rogawski M (2021). "Chapter 24: Antiseizure Drugs". In Katzung B (ed.). Basic and Clinical Pharmacology, 15th Edition. McGraw-Hill Education. pp. 422–455.
  24. ^ Browne TR. Paraldehyde, chlormethiazole, and lidocaine for treatment of status epilepticus. In: Delgado-Escueta AV, Wasterlain CG, Treiman DM, Porter RJ, eds. Status Epilepticus. Mechanisms of Brain Damage and Treatment (Advances in Neurology, Vol 34). New York, Raven Press 1983: 509–517
  25. ^ Ramsay RE (1989). "Pharmacokinetics and clinical use of parenteral phenytoin, phenobarbital, and paraldehyde". Epilepsia. 30 (Suppl 2): S1–S3. doi:10.1111/j.1528-1157.1989.tb05818.x. PMID 2767008. S2CID 44798815.
  26. ^ Plosker GL (November 2012). "Stiripentol: in severe myoclonic epilepsy of infancy (dravet syndrome)". CNS Drugs. 26 (11): 993–1001. doi:10.1007/s40263-012-0004-3. PMID 23018548. S2CID 42911844.
  27. ^ "Public summary of positive opinion for orpphan opinion for orphan designation of stiripentol for the treatment of severe myoclonic epilepsy in infancy" (PDF). European Medicines Agency. 30 July 2007. Archived from the original (PDF) on 17 December 2013. Retrieved 19 May 2013. Doc.Ref.: EMEA/COMP/269/04
  28. ^ a b c d "Diacomit EPAR". European Medicines Agency. Archived from the original on 12 November 2020. Retrieved 8 November 2020.
  29. ^ "Diacomit- stiripentol capsule Diacomit- stiripentol powder, for suspension". DailyMed. 15 May 2020. Archived from the original on 6 August 2020. Retrieved 8 November 2020.
  30. ^ Suddock JT, Kent KJ, Cain MD. Barbiturate Toxicity. 2023 Apr 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan–. PMID 29763050.( 26 / August / 2023 )
  31. ^ Browne TR (May 1976). "Clonazepam. A review of a new anticonvulsant drug". Arch Neurol. 33 (5): 326–32. doi:10.1001/archneur.1976.00500050012003. PMID 817697.
  32. ^ Isojärvi JI, Tokola RA (December 1998). "Benzodiazepines in the treatment of epilepsy in people with intellectual disability". J Intellect Disabil Res. 42 (1): 80–92. PMID 10030438.
  33. ^ Tomson T, Svanborg E, Wedlund JE (May–June 1986). "Nonconvulsive status epilepticus". Epilepsia. 27 (3): 276–85. doi:10.1111/j.1528-1157.1986.tb03540.x. PMID 3698940. S2CID 26694857.
  34. ^ Djurić M, Marjanović B, Zamurović D (May–June 2001). "[West syndrome--new therapeutic approach]". Srp Arh Celok Lek. 129 (1): 72–7. PMID 15637997.
  35. ^ Bourgeois BF, Dodson E, Nordli DR Jr, Pellock JM, Sankar R, eds. (16 December 2007). Pediatric epilepsy: diagnosis and therapy (3rd ed.). New York: Demos Medical Publishing. ISBN 978-1-933864-16-7.
  36. ^ French J, Smith, M, Faught, E, Brown, L (12 May 1999). "Practice advisory: The use of felbamate in the treatment of patients with intractable epilepsy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society". Neurology. 52 (8): 1540–5. doi:10.1212/WNL.52.8.1540. PMID 10331676.
  37. ^ "Felbamate". MedlinePlus : U.S. National Library of Medicine. Archived from the original on 20 May 2013. Retrieved 19 May 2013.
  38. ^ Camerin L, Maleeva G, Gomila-Juaneda A, Suárez-Pereira I, Matera C, Prischich D, Opar E, Riefolo F, Berrocoso E, Gorostiza P (18 June 2024). "Photoswitchable carbamazepine analogs for non-invasive neuroinhibition in vivo". Angewandte Chemie International Edition. doi:10.1002/anie.202403636. hdl:2445/215169. ISSN 1433-7851.
  39. ^ D'Andrea Meira I (2019). "Ketogenic Diet and Epilepsy: What We Know So Far". Frontiers in Neuroscience. 13: 5. doi:10.3389/fnins.2019.00005. PMC 6361831. PMID 30760973.
  40. ^ Pruthi S. "Vagus nerve stimulation". Mayo Clinic. Archived from the original on 20 July 2023. Retrieved 20 July 2023.
  41. ^ a b c d e f AAN Guideline Summary for Clinicians – Efficacy and Tolerability of the New Antiepileptic Drugs, I: Treatment of New Onset Epilepsy Archived 24 February 2011 at the Wayback Machine Retrieved on 29 June 2010
  42. ^ French JA, Kanner AM, Bautista J, et al. (May 2004). "Efficacy and tolerability of the new antiepileptic drugs, I: Treatment of new-onset epilepsy: report of the TTA and QSS Subcommittees of the American Academy of Neurology and the American Epilepsy Society" (PDF). Epilepsia. 45 (5): 401–9. doi:10.1111/j.0013-9580.2004.06204.x. hdl:2027.42/65231. PMID 15101821. S2CID 12259676. Archived from the original on 27 August 2021. Retrieved 30 August 2019.
  43. ^ Eadie M, Bladin P (2001). A Disease Once Sacred: A History of the Medical Understanding of Epilepsy. John Libbey. ISBN 978-0-86196-607-3. Retrieved 29 June 2024.
  44. ^ "New Drug Application (NDA) 008943". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  45. ^ a b c d e f g h i j k l m n o p q r Epilepsy Action: Druglist. Archived 1 March 2011 at the Wayback Machine Retrieved on 1 November 2007.
  46. ^ "New Drug Application (NDA) 205836". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  47. ^ "Drug Approval Package: Briviact (brivaracetam)". U.S. Food and Drug Administration (FDA). 30 March 2016. Archived from the original on 22 November 2019. Retrieved 21 November 2019.
  48. ^ "New Drug Application (NDA) 016608". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019. (Initial approval on 11 March 1968 was for trigeminal neuralgia.)
  49. ^ Schain RJ (1 March 1978). "Pediatrics—Epitomes of Progress: Carbamazepine (Tegretol) in the Treatment of Epilepsy". Western Journal of Medicine. 128 (3): 231–232. PMC 1238063. PMID 18748164.
  50. ^ a b c d e f g h i j k l m Loiseau PJ (June 1999). "Clinical Experience with New Antiepileptic Drugs: Antiepileptic Drugs in Europe". Epilepsia. 40 (Suppl 6): S3–8. doi:10.1111/j.1528-1157.1999.tb00925.x. PMID 10530675. S2CID 29638422.
  51. ^ "New Drug Application (NDA) 202067". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 28 October 2020. Retrieved 21 November 2019.
  52. ^ "Drug Approval Package: Onfi NDA #202067". U.S. Food and Drug Administration (FDA). 20 August 2013. Archived from the original on 22 November 2019. Retrieved 21 November 2019.
  53. ^ "New Drug Application (NDA) 017533". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 20 October 2020. Retrieved 21 November 2019.
  54. ^ "New Drug Application (NDA) 013263". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  55. ^ "New Drug Application (NDA) 018723". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  56. ^ "New Drug Application (NDA) 022416". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 20 October 2020. Retrieved 21 November 2019.
  57. ^ "Drug Approval Package: Brand Name (Generic Name) NDA #". U.S. Food and Drug Administration (FDA). 20 December 2013. Archived from the original on 22 November 2019. Retrieved 21 November 2019.
  58. ^ "New Drug Application (NDA) 012380". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 30 November 2017. Retrieved 21 November 2019.
  59. ^ "New Drug Application (NDA) 010841". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  60. ^ "New Drug Application (NDA) 022334". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 31 October 2020. Retrieved 21 November 2019.
  61. ^ "New Drug Application (NDA) 020189". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 21 October 2020. Retrieved 21 November 2019.
  62. ^ "New Drug Application (NDA) 020450". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 20 October 2020. Retrieved 21 November 2019.
  63. ^ "New Drug Application (NDA) 020235". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  64. ^ "New Drug Application (NDA) 022253". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 20 October 2020. Retrieved 21 November 2019.
  65. ^ "New Drug Application (NDA) 020241". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 24 October 2020. Retrieved 21 November 2019.
  66. ^ "New Drug Application (NDA) 021035". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 21 October 2020. Retrieved 21 November 2019.
  67. ^ a b EPAR: Keppra. Archived 19 June 2009 at the Wayback Machine Retrieved on 1 November 2007.
  68. ^ "New Drug Application (NDA) 006008". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 20 October 2020. Retrieved 21 November 2019.
  69. ^ "New Drug Application (NDA) 008322". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  70. ^ Dodson, W. Edwin, Giuliano Avanzini, Shorvon, Simon D., Fish, David R., Emilio Perucca (2004). The treatment of epilepsy. Oxford: Blackwell Science. xxviii. ISBN 978-0-632-06046-7.
  71. ^ "New Drug Application (NDA) 010596". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  72. ^ "New Drug Application (NDA) 011721". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  73. ^ "New Drug Application (NDA) 021014". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  74. ^ "New Drug Application (NDA) 008762". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 16 December 2020. Retrieved 21 November 2019. (Marketed in 1938, approved 1953)
  75. ^ "New Drug Application (NDA) 008855". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 26 July 2020. Retrieved 21 November 2019.
  76. ^ Kutt, Henn, Resor, Stanley R. (1992). The Medical treatment of epilepsy. New York: Dekker. p. 385. ISBN 978-0-8247-8549-9. (first usage)
  77. ^ "New Drug Application (NDA) 021446". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 20 October 2020. Retrieved 21 November 2019.
  78. ^ a b EPAR: Lyrica Archived 21 June 2009 at the Wayback Machine Retrieved on 1 November 2007.
  79. ^ "New Drug Application (NDA) 009170". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 24 October 2020. Retrieved 21 November 2019.
  80. ^ "New Drug Application (NDA) 021911". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  81. ^ "Drug Approval Package: Banzel (Rufinamide) NDA #021911". U.S. Food and Drug Administration (FDA). 30 May 2012. Archived from the original on 22 November 2019. Retrieved 21 November 2019.
  82. ^ "New Drug Application (NDA) 206709". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 26 July 2020. Retrieved 21 November 2019.
  83. ^ "Drug Approval Package: Diacomit (stiripentol)". U.S. Food and Drug Administration (FDA). 7 September 2018. Archived from the original on 22 November 2019. Retrieved 21 November 2019.
  84. ^ "New Drug Application (NDA) 020646". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 16 December 2020. Retrieved 21 November 2019.
  85. ^ "NDA: 020646". DrugPatentWatch. Archived from the original on 23 March 2021. Retrieved 19 May 2013.
  86. ^ "New Drug Application (NDA) 020505". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  87. ^ "New Drug Application (NDA) 005856". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  88. ^ "New Drug Application (NDA) 018081". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  89. ^ "New Drug Application (NDA) 020427". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 20 October 2020. Retrieved 21 November 2019.
  90. ^ "New Drug Application (NDA) 020789". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on 19 October 2020. Retrieved 21 November 2019.
  91. ^ a b EPAR: Zonegran. Archived 13 July 2009 at the Wayback Machine Retrieved on 1 November 2007
  92. ^ a b Bromley R, Adab N, Bluett-Duncan M, Clayton-Smith J, Christensen J, Edwards K, Greenhalgh J, Hill RA, Jackson CF, Khanom S, McGinty RN, Tudur Smith C, Pulman J, Marson AG (29 August 2023). "Monotherapy treatment of epilepsy in pregnancy: congenital malformation outcomes in the child". The Cochrane Database of Systematic Reviews. 2023 (8): CD010224. doi:10.1002/14651858.CD010224.pub3. ISSN 1469-493X. PMC 10463554. PMID 37647086.
  93. ^ a b c Harden CL, Pennell PB, Koppel BS, et al. (May 2009). "Management issues for women with epilepsy—focus on pregnancy (an evidence-based review): III. Vitamin K, folic acid, blood levels, and breast-feeding: Report of the Quality Standards Subcommittee and Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the American Epilepsy Society". Epilepsia. 50 (5): 1247–55. doi:10.1111/j.1528-1167.2009.02130.x. PMID 19507305. S2CID 221731995.
  94. ^ George IC (2017). "Practice Current: How do you treat epilepsy in pregnancy?". Neurology: Clinical Practice. 7 (4): 363–371. doi:10.1212/cpj.0000000000000387. ISSN 2163-0402. PMC 5648199. PMID 29185530.
  95. ^ a b c Bromley R, Weston J, Adab N, Greenhalgh J, Sanniti A, McKay AJ, Tudur Smith C, Marson AG (2014). "Treatment for epilepsy in pregnancy: neurodevelopmental outcomes in the child". Reviews. 2020 (10): CD010236. doi:10.1002/14651858.CD010236.pub2. PMC 7390020. PMID 25354543.
  96. ^ Tomson T, Marson A, Boon P, Canevini MP, Covanis A, Gaily E, Kälviäinen R, Trinka E (July 2015). "Valproate in the treatment of epilepsy in girls and women of childbearing potential". Epilepsia. 56 (7): 1006–1019. doi:10.1111/epi.13021. ISSN 0013-9580. PMID 25851171. Archived from the original on 1 March 2024. Retrieved 1 March 2024.
  97. ^ Birnbaum AK, Meador KJ, Karanam A, Brown C, May RC, Gerard EE, Gedzelman ER, Penovich PE, Kalayjian LA, Cavitt J, Pack AM, Miller JW, Stowe ZN, Pennell PB, for the MONEAD Investigator Group (1 April 2020). "Antiepileptic Drug Exposure in Infants of Breastfeeding Mothers With Epilepsy". JAMA Neurology. 77 (4): 441–450. doi:10.1001/jamaneurol.2019.4443. ISSN 2168-6149. PMC 6990802. PMID 31886825.
  98. ^ "Norwegian Mother, Father and Child Cohort Study (MoBa)". Norwegian Institute of Public Health. Archived from the original on 12 October 2023. Retrieved 11 October 2023.
  99. ^ Tomson T, Battino D, Perucca E (April 2019). "Teratogenicity of antiepileptic drugs". Current Opinion in Neurology. 32 (2): 246–252. doi:10.1097/WCO.0000000000000659. ISSN 1473-6551. PMID 30664067. S2CID 58608931. Archived from the original on 22 November 2023. Retrieved 31 December 2023.
  100. ^ Pennell PB, Karanam A, Meador KJ, Gerard E, Kalayjian L, Penovich P, Matthews A, McElrath TM, Birnbaum AK, MONEAD Study Group (1 April 2022). "Antiseizure Medication Concentrations During Pregnancy: Results From the Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) Study". JAMA Neurology. 79 (4): 370–379. doi:10.1001/jamaneurol.2021.5487. ISSN 2168-6149. PMC 8845026. PMID 35157004.
  101. ^ Jazayeri D, Graham J, Hitchcock A, O'Brien TJ, Vajda FJ (2018). "Outcomes of pregnancies in women taking antiepileptic drugs for non-epilepsy indications". Seizure. 56: 111–114. doi:10.1016/j.seizure.2018.02.009. ISSN 1059-1311. PMID 29471258.
  102. ^ Bittigau P, Sifringer M, Genz K, et al. (May 2002). "Antiepileptic drugs and apoptotic neurodegenereation in the developing brain". Proceedings of the National Academy of Sciences of the United States of America. 99 (23): 15089–94. Bibcode:2002PNAS...9915089B. doi:10.1073/pnas.222550499. PMC 137548. PMID 12417760.
  103. ^ Manthey D, Asimiadou S, et al. (June 2005). "Sulthiame but not levetiracetam exerts neurotoxic effect in the developing rat brain". Exp Neurol. 193 (2): 497–503. doi:10.1016/j.expneurol.2005.01.006. PMID 15869952. S2CID 1493015.
  104. ^ Katz I, Kim J, et al. (August 2007). "Effects of lamotrigine alone and in combination with MK-801, phenobarbital, or phenytoin on cell death in the neonatal rat brain". J Pharmacol Exp Ther. 322 (2): 494–500. doi:10.1124/jpet.107.123133. PMID 17483293. S2CID 12741109.
  105. ^ Kim J, Kondratyev A, Gale K (October 2007). "Antiepileptic drug-induced neuronal cell death in the immature brain: effects of carbamazepine, topiramate, and levetiracetam as monotherapy versus polytherapy". J Pharmacol Exp Ther. 323 (1): 165–73. doi:10.1124/jpet.107.126250. PMC 2789311. PMID 17636003.
  106. ^ Forcelli PA, Kim J, et al. (December 2011). "Pattern of antiepileptic drug-induced cell death in limbic regions of the neonatal rat brain". Epilepsia. 52 (12): e207–11. doi:10.1111/j.1528-1167.2011.03297.x. PMC 3230752. PMID 22050285.

Further reading

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  • Anti epileptic activity of novel substituted fluorothiazole derivatives by Devid Chutia, RGUHS
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