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| Clinical data | |
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| Pronunciation | /ləˈmoʊtrᵻˌdʒiːn/ |
| Trade names | Originally Lamictal, many brands worldwide[1] |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a695007 |
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| Routes of administration |
Oral |
| ATC code | N03AX09 (WHO) |
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| Pharmacokinetic data | |
| Bioavailability | 98% |
| Protein binding | 55% |
| Metabolism | Hepatic (mostly UGT1A4-mediated) |
| Biological half-life | 29 hours |
| Excretion | Urine (65%), faeces (2%) |
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| CAS Number | 84057-84-1 Y |
| PubChem (CID) | 3878 |
| IUPHAR/BPS | 2622 |
| DrugBank | DB00555 N |
| ChemSpider | 3741 Y |
| UNII | U3H27498KS Y |
| KEGG | D00354 Y |
| ChEBI | CHEBI:6367 N |
| ChEMBL | CHEMBL741 Y |
| ECHA InfoCard | 100.074.432 |
| Chemical and physical data | |
| Formula | C9H7Cl2N5 |
| Molar mass | 256.091 g/mol |
| 3D model (Jmol) | Interactive image |
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Lamotrigine, originally marketed as Lamictal and available under many brands worldwide,[1] is an anticonvulsant drug used in the treatment of epilepsy and bipolar disorder. It is also used off-label as an adjunct in treating clinical depression.[2] For epilepsy, it is used to treat focal seizures, primary and secondary tonic-clonic seizures, and seizures associated with Lennox-Gastaut syndrome. Like many other anticonvulsant medications, lamotrigine also seems to act as an effective mood stabilizer, and has been the first US Food and Drug Administration (FDA)-approved drug for this purpose since lithium, a drug approved almost 30 years earlier. It is approved for the maintenance treatment of bipolar type I.
Lamotrigine is a synthetic phenyltriazine with anti-epileptic and analgesic properties. Lamotrigine enhances the action of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, which may result in a reduction of pain-related transmission of signals along nerve fibers. This agent may also inhibit voltage-gated sodium channels, suppress glutamate release, and inhibit serotonin reuptake.[3] It is generally accepted to be a member of the sodium channel blocking class of antiepileptic drugs,[4] but it could have additional actions since it has a broader spectrum of action than other sodium channel antiepileptic drugs such as phenytoin and carbamazepine and is effective in the treatment of the depressed phase of bipolar disorder, whereas other sodium channel blocking antiepileptic drugs are not, possibly on account of its sigma receptor activity. In addition, lamotrigine shares few side-effects with other, unrelated anticonvulsants known to inhibit sodium channels, which further emphasises its unique properties.[5] Lamotrigine is inactivated by glucuronidation in the liver.[6]
Lamotrigine was developed in 1994.[7]
Contents
- 1 Medical uses
- 1.1 Epilepsy
- 1.2 Bipolar disorder
- 1.3 Other uses
- 2 Side effects
- 2.1 Effects in women
- 2.2 Pregnancy and breastfeeding
- 2.3 Other types of effects
- 3 Mechanism of action
- 4 Pharmacokinetics
- 5 History
- 6 Trade names
- 7 References
- 8 External links
Medical uses
Epilepsy
Lamotrigine is approved in the US for the treatment of partial seizures.[8] It is considered a first-line drug for primary generalised tonic-clonic seizures (includes simple partial, complex partial and secondarily generalised seizures), and as an adjuvant therapy in partial seizures (focal onset tonic-clonic, atypical absence, myoclonic, and due to Lennox-Gastaut syndrome). As well, it is used as an alternative drug for absence seizure and atypical absence, myoclonic, and atonic seizures.[9][10]
Lamotrigine is one of a small number of FDA-approved therapies for seizures associated with Lennox-Gastaut syndrome, a severe form of epilepsy. Typically developing before four years of age, LGS is associated with developmental delays. There is no cure, treatment is often complicated, and complete recovery is rare. Symptoms include the atonic seizure (also known as a "drop attack"), during which brief loss of muscle tone and consciousness cause abrupt falls. Lamotrigine significantly reduces the frequency of LGS seizures, and is one of two medications known to decrease the severity of drop attacks.[11] Combination with valproate is common, but this increases the risk of lamotrigine-induced rash, and necessitates reduced dosing due to the interaction of these drugs.[12]
Bipolar disorder
Lamotrigine is approved in the US for maintenance treatment of bipolar I disorder.[13] While traditional anticonvulsant drugs are predominantly antimanics, lamotrigine is most effective for preventing the recurrent depressive episodes of bipolar disorder. The drug seems ineffective in the maintenance of current rapid-cycling, acute mania, or acute depression in bipolar disorder; however, it is effective at prevention of or delaying the mania, depressive, or rapid cycle.[14] According to studies in 2007, lamotrigine may treat bipolar depression without triggering mania, hypomania, mixed states, or rapid-cycling.[15]
There is less evidence of therapeutic benefit when lamotrigine is used to treat a current mood episode. It has not demonstrated effectiveness in treating acute mania,[16] and there is controversy regarding the drug’s effectiveness in treating acute bipolar depression.[17] While the 2002 American Psychiatric Association (APA) guidelines recommend lamotrigine as a first-line treatment for acute depression in Bipolar II disorder,[18] the APA’s website notes that the guidelines, being more than five years old, “can no longer be assumed to be current".[19] A paper written in 2008 by Nasser et al. reviewed evidence from trials that were unpublished and not referenced in the 2002 APA guidelines, and it concludes that lamotrigine has "very limited, if any, efficacy in the treatment of acute bipolar depression".[14] A 2008 paper by Calabrese et al. examined much of the same data, and found that in five placebo-controlled studies, lamotrigine did not significantly differ from placebo in the treatment of bipolar depression.[20] However, in a meta-analysis of these studies conducted in 2008, Calabrese found that lamotrigine was effective in individuals with bipolar depression, with a number needed to treat (NNT) of 11, or 7 in severe depression.[21]
A 2013 review about lamotrigine concluded that it is recommended in bipolar maintenance when depression is prominent and that more research is needed in regards to its role in the treatment of acute bipolar depression and unipolar depression. Furthermore, no information to recommend its use in other psychiatric disorders was found.[22]
Other uses
Off-label uses include the treatment of peripheral neuropathy, trigeminal neuralgia, cluster headaches, migraines, and reducing neuropathic pain.[23][24][25] Off-label psychiatric usage includes the treatment of treatment-resistant obsessive-compulsive disorder,[26] depersonalization disorder,[27] hallucinogen persisting perception disorder,[28] schizoaffective disorder,[29] borderline personality disorder,[30] and post-traumatic stress disorder.[31] Lamotrigine has been studied as an adjunctive therapy for treatment of refractory unipolar depression, attaining efficacy on the secondary metric for treatment outcomes (Clinical Global Impressions), but not the primary metrics (Montgomery–Åsberg Depression Rating Scale and Hamilton Rating Scale for Depression).[2] In at least two cases, lamotrigine seemed efficacious for Kleine-Levin syndrome[32][33] but caused no improvement in at least one case.[34]
Lamotrigine has also been found to have a role in the treatment of adult attention deficit hyperactivity disorder with comorbid depression.[35]
It is also appropriate for the treatment of Lennox–Gastaut syndrome.[36]
Side effects
Lamotrigine prescribing information has a black box warning about life-threatening skin reactions, including Stevens–Johnson syndrome, DRESS syndrome and toxic epidermal necrolysis.[37] The manufacturer states that nearly all cases appear in the first two to eight weeks of therapy,[37] or if the medication is suddenly stopped then resumed at the normal dosage.[citation needed] Patients should seek medical attention for any unexpected skin rash, as its presence is an indication of a possible serious or even deadly side-effect of the drug. Not all rashes that occur while taking lamotrigine progress to SJS or TEN. Between 5 and 10% of patients will develop a rash, but only one in a thousand patients will develop a serious rash. Rash and other skin reactions are more common in children, so this medication is often reserved for adults. For patients whose lamotrigine has been stopped after development of a rash, re-challenge with lamotrigine is also a viable option. However, it is not applicable for very serious cases.[38]
There is also an increased incidence of these eruptions in patients who are currently on, or recently discontinued a valproate-type anticonvulsant drug, as these medications interact in such a way that the clearance of both is decreased and the effective dose of lamotrigine is increased.[37]
Side-effects such as rash, fever, and fatigue are very serious, as they may indicate incipient Stevens–Johnson syndrome, toxic epidermal necrolysis, DRESS syndrome or aseptic meningitis.[39]
Other side-effects include loss of balance or coordination; double vision; crossed eyes; pupil constriction; blurred vision; dizziness and lack of coordination; drowsiness, insomnia; anxiety; vivid dreams or nightmares; dry mouth, mouth ulcers;[37] memory problems; mood changes; runny nose; cough; nausea, indigestion, abdominal pain, weight loss; missed or painful menstrual periods; and vaginitis. The side-effect profile varies for different patient populations.[39] Overall adverse effects in treatment are similar between men, women, geriatric, pediatric and racial groups.[40]
Lamotrigine has been associated with a decrease in white blood cell count (leukopenia).[41] Lamotrigine does not prolong QT/QTc in TQT studies in healthy subjects.[42]
Cases of lamotrigine-induced neuroleptic malignant syndrome have been reported.[43][44]
Effects in women
In clinical trials women were more likely than men to have side-effects.[45] This is the opposite of most other anticonvulsants.
There is evidence showing interactions between lamotrigine and female hormones, which can be of particular concern for women on estrogen-containing hormonal contraceptives. Ethinylestradiol, the ingredient of such contraceptives, has been shown to decrease serum levels of lamotrigine.[46] Women starting an estrogen-containing oral contraceptive may need to increase the dosage of lamotrigine to maintain its level of efficacy. Likewise, women may experience an increase in lamotrigine side-effects upon discontinuation of the pill. This may include the "pill-free" week where lamotrigine serum levels have been shown to increase twofold.[37] Another study showed a significant increase in follicle stimulating hormone (FSH) and luteinizing hormone (LH) in women taking lamotrigine with oral contraceptive compared to women taking oral contraceptives alone.[47] However, these increases were not in conjunction with increased progesterone, indicating that oral contraceptives maintained suppression of ovulation.[47]
Pregnancy and breastfeeding
Lamotrigine is rated Pregnancy Category Risk C. Use during pregnancy is recommended only if benefits outweigh potential risks. In September 2006, the FDA issued a warning stating that taking lamotrigine during the first trimester of pregnancy may increase the risk for cleft lip and palate malformation in newborns.[48] Since then, review studies have found that overall rates of congenital malformations in infants exposed to lamotrigine in utero are relatively low (1-4%).[49][50] This compares to a typical 3% rate in the untreated population. A prospective study on cognition in children (mean age = 4.2 years) exposed to lamotrigine in utero did not indicate any adverse effects.[51]
Lamotrigine is expressed in breast milk; the manufacturer does not recommend breastfeeding during treatment. In "Medications and Mothers' Milk," a frequently updated review of scientific literature, lamotrigine is rated as L3: moderately safe.[52]
Other types of effects
Lamotrigine binds to melanin-containing tissues such as the iris of the eye. The long-term consequences of this are unknown.[53]
Some patients have reported experiencing a loss of concentration, even with very small doses. Lamotrigine has been implicated in the apoptotic neurodegeneration of the developing brain.[54] GlaxoSmithKline investigated lamotrigine for the treatment of ADHD with inconclusive results. No detrimental effects on cognitive function were observed; however, the only statistical improvement in core ADHD symptoms was an improvement on a test, PASAT (Paced Auditory Serial Addition Test), that measures auditory processing speed and calculation ability.[55] Another study reported that lamotrigine might be a safe and effective treatment option for adult ADHD comorbid with bipolar and recurrent depression.[56]
Lamotrigine is known to affect sleep. Studies with small numbers (10-15) of patients reported that lamotrigine increases sleep stability (increases the duration of REM sleep, decreases the number of phase shifts and decreases the duration of slow-wave sleep),[57] and that there was no effect on vigilance,[58] and daytime somnolence and cognitive function.[59] However, a retrospective study of 109 patients' medical records found that 6.7% of patients experienced an "alerting effect" resulting in intolerable insomnia, for which the treatment had to be discontinued.[60]
Lamotrigine can induce a type of seizure known as a myoclonic jerk, which tends to happen soon after the use of the medication.[61] When used in the treatment of myoclonic epilepsies such as juvenile myoclonic epilepsy, lower doses (and lower plasma levels) are usually needed, as even moderate doses of this drug can induce seizures, including tonic-clonic seizures, which can develop into status epilepticus, which is a medical emergency. It can also cause myoclonic status epilepticus.[40]
In overdose, lamotrigine can cause uncontrolled seizures in most people. Reported results in overdoses involving up to 15 g include increased seizures, coma and death.[40]
Mechanism of action
Lamotrigine, 150 mg tablet.
Lamotrigine is a member of the sodium channel blocking class of antiepileptic drugs.[62] It is a triazine derivate that inhibits voltage-sensitive sodium channels, leading to stabilization of neuronal membranes. It also blocks L-, N-, and P-type calcium channels and has weak 5-hydroxytryptamine-3 (5-HT3) receptor inhibition. These actions are thought to inhibit release of glutamate at cortical projections in the ventral striatum limbic areas,[63] and its neuroprotective and antiglutamatergic effects have been pointed out as promising contributors to its mood stabilizing activity.[64] Observations that lamotrigine reduced γ-aminobutyric acid (GABA) A receptor-mediated neurotransmission in rat amygdala,[65] suggest that a GABAergic mechanism may also be involved, although this concept is controversial.[66]
Lamotrigine does not have pronounced effects on any of the usual neurotransmitter receptors (adrenergic, dopamine D1 and D2, muscarinic, GABA, histaminergic H1, serotonin 5-HT2, and N-methyl-D-asparate). Inhibitory effects on 5-HT, norepinephrine, and dopamine transporters are weak.[67] Lamotrigine is a weak inhibitor of dihydrofolate reductase,[68] but whether this effect is sufficient to contribute to a mechanism of action or increases risk to the fetus during pregnancy is not known. Early studies of lamotrigine's mechanism of action examined its effects on the release of endogenous amino acids from rat cerebral cortex slices in vitro. As is the case for antiepileptic drugs that act on voltage-dependent sodium channels, lamotrigine inhibited the release of glutamate and aspartate evoked by the sodium-channel activator veratrine and was less effective in the inhibition of acetylcholine or GABA release. At high concentrations, it had no effect on spontaneous or potassium evoked amino acid release.[45]
These studies suggested that lamotrigine acts presynaptically on voltage-gated sodium channels to decrease glutamate release. Several electrophysiological studies have investigated the effects of lamotrigine on voltage-dependent sodium channels. For example, lamotrigine blocked sustained repetitive firing in cultured mouse spinal cord neurons in a concentration-dependent manner, at concentrations that are therapeutically relevant in the treatment of human seizures. In cultured hippocampal neurons, lamotrigine reduced sodium currents in a voltage-dependent manner, and at depolarised potentials showed a small frequency-dependent inhibition. These and a variety of other results indicate that the antiepileptic effect of lamotrigine, like that of phenytoin and carbamazepine, is at least in part due to use- and voltage-dependent modulation of fast voltage-dependent sodium currents. However, lamotrigine has a broader clinical spectrum of activity than phenytoin and carbamazepine and is recognised to be protective against generalised absence epilepsy and other generalised epilepsy syndromes, including primary generalised tonic–clonic seizures, juvenile myoclonic epilepsy, and Lennox-Gastaut syndrome.
The basis for this broader spectrum of activity of lamotrigine is unknown, but could relate to actions of the drug on voltage-activated calcium channels. Lamotrigine blocks T-type calcium channels weakly, if at all. However, it does inhibit native and recombinant high-voltage–activated calcium channels (N- and P/Q/R-types) at therapeutic concentrations. Whether this activity on calcium channels accounts for lamotrigine's broader clinical spectrum of activity in comparison with phenytoin and carbamazepine remains to be determined.
It antagonises the following receptors with the following IC50 values:[68]
- 5-HT3, IC50=18μM
- σ receptors, IC50=145μM
Pharmacokinetics
The pharmacokinetics of lamotrigine follow first-order kinetics, with a half-life of 29 hours and volume of distribution of 1.36 L/kg.[69] Lamotrigine is rapidly and completely absorbed after oral administration. Its absolute bioavailability is 98% and its plasma Cmax occurs from 1.4 to 4.8 hours. Available data indicate that its bioavailability is not affected by food. Estimate of the mean apparent volume of distribution of lamotrigine following oral administration ranges from 0.9 to 1.3 L/kg. This is independent of dose and is similar following single and multiple doses in both patients with epilepsy and in healthy volunteers.[70]
Lamotrigine is metabolised predominantly by glucuronic acid conjugation. Its major metabolite is an inactive 2-n-glucuronide conjugate.[71] Lamotrigine has fewer drug interactions than many anticonvulsant drugs, although pharmacokinetic interactions with carbamazepine, phenytoin and other hepatic enzyme inducing medications may shorten half-life.[72] Dose adjustments should be made on clinical response, but monitoring may be of benefit in assessing compliance.[45]
The capacity of available tests to detect potentially adverse consequences of melanin binding is unknown. Clinical trials excluded subtle effects and optimal duration of treatment. There are no specific recommendations for periodic ophthalmological monitoring. Lamotrigine binds to the eye and melanin-containing tissues which can accumulate over time and may cause toxicity. Prescribers should be aware of the possibility of long-term ophthalmologic effects and base treatment on clinical response. Patient compliance should be periodically reassessed with lab and medical testing of liver and kidney function to monitor progress or side effects.[45]
History
- December 1994 — Lamotrigine was approved for the treatment of partial seizures.[8]
- August 1998 — for use as adjunctive treatment of Lennox-Gastaut syndrome in pediatric and adult patients, new dosage form: chewable dispersible tablets.
- December 1998 — for use as monotherapy for treatment of partial seizures in adult patients when converting from a single enzyme-inducing anti-epileptic drug (EIAED).
- January 2003 — for use as adjunctive therapy for partial seizures in pediatric patients as young as two years of age.
- June 2003 — approved for maintenance treatment of Bipolar I disorder; the first such medication since lithium.[13]
- January 2004 — for use as monotherapy for treatment of partial seizures in adult patients when converting from the anti-epileptic drug valproate [including valproic acid (Depakene); sodium valproate (Epilim) and divalproex sodium (Depakote)].
Trade names
Lamictal 200 mg tablets
Lamotrigine was originally brought to market by GlaxoSmithKline's trademarked as Lamictal; it also available in generic form under many brand names worldwide.[1][73]
References
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- ^ a b Barbosa L, Berk M, Vorster M (April 2003). "A double-blind, randomised, placebo-controlled trial of augmentation with lamotrigine or placebo in patients concomitantly treated with fluoxetine for resistant major depressive episodes" (PDF). J Clin Psychiatry. 64 (4): 403–7. doi:10.4088/JCP.v64n0407. PMID 12716240.
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- ^ Berwaerts, K; Sienaert P; De Fruyt J (2009). "Teratogenic effects of lamotrigine in women with bipolar disorder". Tijdschr Psychiatr (in Dutch). 51 (10): 741–50. PMID 19821242.
- ^ Prakash; Prabhu LV; Nasar MA; et al. (October 2007). "Lamotrigine in pregnancy: safety profile and the risk of malformations". Singapore Med J. 48 (10): 880–3. PMID 17909669.
- ^ McVearry, KM; Gaillard WD; VanMeter J; Meador KJ (December 2009). "A prospective study of cognitive fluency and originality in children exposed in utero to carbamazepine, lamotrigine, or valproate monotherapy". Epilepsy Behav. 16 (4): 609–16. doi:10.1016/j.yebeh.2009.09.024. PMID 19892603.
- ^ Hale, TW (2008). Medications and Mothers' Milk (13th ed.). Hale Publishing. p. 532. ISBN 978-0-9815257-2-3.
- ^ anonymous. "Lamictal, Warnings & Precautions". RxList Inc. Retrieved 2008-04-09.
- ^ "The mechanisms by which AEDs affect cognition and the measures to prevent the adverse effects in immature rats". Archived from the original on June 25, 2013.
- ^ Glaxo Smith Klein Clinical Study Register, Study No. LAM40120: Lamotrigine (Lamictal®) Treatment in adults with Attention Deficit Hyperactivity Disorder (ADHD), A pilot study
- ^ Oncü B, Er O, Colak B, Nutt DJ (2014). "Lamotrigine for attention deficit-hyperactivity disorder comorbid with mood disorders: a case series.". J Psychopharmacol. 28 (3): 282–3. doi:10.1177/0269881113493365. PMID 23784736.
- ^ Foldvary, N; Perry M; Lee J; et al. (December 2001). "The effects of lamotrigine on sleep in patients with epilepsy". Epilepsia. 42 (12): 1569–73. doi:10.1046/j.1528-1157.2001.46100.x. PMID 11879368.
- ^ Bonanni, E; Galli R; Gori S; et al. (June 2001). "Neurophysiological evaluation of vigilance in epileptic patients on monotherapy with lamotrigine". Clin Neurophysiol. 112 (6): 1018–22. doi:10.1016/S1388-2457(01)00537-5. PMID 11377260.
- ^ Placidi, F; Marciani MG; Diomedi M; et al. (August 2000). "Effects of lamotrigine on nocturnal sleep, daytime somnolence and cognitive functions in focal epilepsy". Acta Neurol Scand. 102 (2): 81–6. doi:10.1034/j.1600-0404.2000.102002081.x. PMID 10949523.
- ^ Sadler, M (March 1999). "Lamotrigine associated with insomnia". Epilepsia. 40 (3): 322–5. doi:10.1111/j.1528-1157.1999.tb00712.x. PMID 10080513.
- ^ http://www.ehealthme.com/ds/lamictal/myoclonic+jerks Retrieved August 19, 2010. Myoclonic Jerk in the use of Lamictal.
- ^ Rogawski M (2002). "Chapter 1: Principles of antiepileptic drug action". In Levy RH, Mattson RH, Meldrum BS, Perucca E. Antiepileptic Drugs, Fifth Edition. Lippincott Williams & Wilkins. pp. 3–22. ISBN 9780781723213.
- ^ Thomas, SP; Nandhra HS; Jayaraman A (April 2010). "Systematic review of lamotrigine augmentation of treatment resistant unipolar depression (TRD)". J Ment Health. 19 (2): 168–75. doi:10.3109/09638230903469269. PMID 20433324.
- ^ Ketter, TA; Manji HK; Post RM (October 2003). "Potential mechanisms of action of lamotrigine in the treatment of bipolar disorders". J Clin Psychopharmacol. 23 (5): 168–75. doi:10.1097/01.jcp.0000088915.02635.e8. PMID 14520126.
- ^ Braga, MF; Aroniadou-Anderjaska V; Post RM; Li H (March 2002). ". Lamotrigine reduces spontaneous and evoked GABAA receptor-mediated synaptic transmission in the basolateral amygdala: implications for its effects in seizure and affective disorders". Neuropharmacology. 42 (4): 522–9. doi:10.1016/s0028-3908(01)00198-8. PMID 11955522.
- ^ Shiah, IS; Yatham LN; Gau YC; Baker GB (May 2003). "Potential mechanisms of action of lamotrigine in the treatment of bipolar disorders". Prog Neuropsychopharmacol Biol Psychiatry. 27 (3): 419–23. doi:10.1016/S0278-5846(03)00028-9. PMID 12691776.
- ^ Southam, E; Kirkby D; Higgins GA; Hagan RM (Sep 1998). "Lamotrigine inhibits monoamine uptake in vitro and modulates 5-hydroxytryptamine uptake in rats". Eur J Pharmacol. 25 (358(1)): 19–24. PMID 9809864.
- ^ a b "LAMICTAL (lamotrigine) tablet". Daily Med. U.S. National Library of Medicine. Retrieved 2013-12-26.
- ^ Ramsay RE, Pellock JM, Garnett WR, et al. (1991). "Pharmacokinetics and safety of lamotrigine (Lamictal) in patients with epilepsy". Epilepsy Res. 10 (2–3): 191–200. doi:10.1016/0920-1211(91)90012-5. PMID 1817959.
- ^ Cohen, AF; Land GS; Breimer DD; Yuen WC; Winton C; Peck AW (Nov 1987). "Lamotrigine, a new anticonvulsant: pharmacokinetics in normal humans". Clin Pharmacol Ther. 42 (5): 535–41. doi:10.1038/clpt.1987.193. PMID 3677542.
- ^ Goa, KL; Ross SR; Chrisp P (Jul 1993). "A review of its pharmacological properties and clinical efficacy in epilepsy". Drugs. 46 (1): 152–76. doi:10.2165/00003495-199346010-00009. PMID 7691504.
- ^ Anderson, GD (May 1998). "A mechanistic approach to antiepileptic drug interactions.". Pharmacother. 32 (5): 554–63. doi:10.1345/aph.17332. PMID 9606477.
- ^ anonymous (2 March 2005). "Treatment for epilepsy: generic lamotrigine". Department of Health (UK). Retrieved 2008-04-09.
External links
- FAQ: Psychiatric Uses of Lamotrigine (Lamictal), by Ivan K. Goldberg, MD. Includes many references from the medical literature.
- Center for Drug Evaluation and Research: Lamictal — documents related to the FDA approval process, including medical reviews and correspondence letters.
- Epilepsy South Africa: MEDICATION FOR EPILEPSY — an Epilepsy FAQ with a list of medicines for treatment thereof, includes lamotrigine with South African trade name Lamictin
- Adverse Reactions — Reported adverse reactions and side-effects.
- U.S. National Library of Medicine: Drug Information Portal — Lamotrigine
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UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. Pediatric bipolar major depression: Choosing treatment
- 2. Pediatric bipolar disorder: Overview of choosing treatment
- 3. 成人における双極性障害：急性うつ病の薬物療法 bipolar disorder in adults pharmacotherapy for acute depression
- 4. Antiseizure drugs: Mechanism of action, pharmacology, and adverse effects
- 5. Pediatric bipolar disorder and pharmacotherapy: General principles
English Journal
- The antiepileptic drug lamotrigine is a substrate of mouse and human breast cancer resistance protein (ABCG2).
- Römermann K1, Helmer R2, Löscher W3.
- Neuropharmacology.Neuropharmacology.2015 Jun;93:7-14. doi: 10.1016/j.neuropharm.2015.01.015. Epub 2015 Jan 31.
- Resistance to antiepileptic drugs (AEDs) is the major problem in the treatment of epilepsy. One hypothesis to explain AED resistance suggests that seizure-induced overexpression of efflux transporters at the blood-brain barrier (BBB) restricts AEDs to reach their brain targets. Various studies exami
- PMID 25645391
- Retention rate of zonisamide in intractable epilepsy.
- Nakken KO1, Lindstrøm P, Andersen H.
- Acta neurologica Scandinavica.Acta Neurol Scand.2015 May;131(5):268-74. doi: 10.1111/ane.12379. Epub 2015 Feb 3.
- OBJECTIVES: To assess the effect and tolerability of zonisamide (ZNS) as adjunctive treatment for difficult-to-treat epilepsy in adult Scandinavian patients.MATERIAL AND METHODS: 151 outpatients (mean age: 42.5 years) from 18 centres in Denmark, Sweden and Norway were recruited to the study. 81.5%
- PMID 25644477
- Chemical inhibition of bacterial ribosome biogenesis shows efficacy in a worm infection model.
- Stokes JM1, Selin C2, Cardona ST3, Brown ED4.
- Antimicrobial agents and chemotherapy.Antimicrob Agents Chemother.2015 May;59(5):2918-20. doi: 10.1128/AAC.04690-14. Epub 2015 Feb 23.
- The development of antibacterial compounds that perturb novel processes is an imperative in the challenge presented by widespread antibiotic resistance. While many antibiotics target the ribosome, molecules that inhibit ribosome assembly have yet to be used in this manner. Here we show that a novel
- PMID 25712357
Japanese Journal
- 私が歩んだ向精神薬開発の道 : 秘話でつづる向精神薬開発の歴史(第72回)新規抗てんかん薬の開発物語(その3)抗マラリア薬開発の中から創成されたlamotrigine(2)双極性障害への大開発物語
- 臨床精神薬理 20(7), 841-852, 2017-07
- NAID 40021255900
- 私が歩んだ向精神薬開発の道 : 秘話でつづる向精神薬開発の歴史(第71回)新規抗てんかん薬の開発物語(その3)抗マラリア薬開発の中から創成されたlamotrigine(1)Lamotrigineの発見から抗てんかん薬として大成するまで
- 臨床精神薬理 20(6), 711-732, 2017-06
- NAID 40021231239
- 医薬品副作用被害救済制度を活用するために (特集 法・制度からみた臨床精神医学)
- 臨床精神医学 = Japanese journal of clinical psychiatry 46(4), 403-408, 2017-04
- NAID 40021170584
Related Links
- Lamotrigine is an anti-epileptic medication, also called an anticonvulsant. Lamotrigine is used alone or with other medications to treat epileptic seizures in adults and children. Lamotrigine is also used to delay mood episodes in adults ...
- Lamotrigine extended-release (long-acting) tablets are used with other medications to treat certain types of seizures in patients who have epilepsy. All types of lamotrigine tablets (tablets, orally disintegrating tablets, and chewable ...
- Lamotrigine (Lamictal, Lamictal CD, Lamictal ODT, Lamictal XR) is prescribed for treating seizures and mood episodes in people with bipolar disorder. Side effects, dosing, drug interactions are reviewed. ... The dose of immediate ...
Related Pictures
★リンクテーブル★
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