Relevant bibliographies by topics / Carbamazepine

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Carbamazepine'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Carbamazepine"

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Eimer, Michelle, and Barry L. Carter. "Elevated Serum Carbamazepine Concentrations following Diltiazem Initiation." Drug Intelligence & Clinical Pharmacy 21, no. 4 (1987): 340–42. http://dx.doi.org/10.1177/106002808702100408.

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A case of carbamazepine neurotoxicity following the addition of diltiazem is reported. A patient with previously stable carbamazepine serum concentrations was treated with diltiazem for atrial fibrillation and a rapid ventricular response. After three days on the combined regimen, the patient developed neurological symptoms resulting in hospitalization. After a review of the patient's medication usage and carbamazepine concentrations, an interaction between diltiazem and carbamazepine was suspected. Carbamazepine's elimination appears to have been decreased, resulting in neurotoxicity. The tox
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Citrome, Leslie. "Use of Lithium, Carbamazepine, and Valproic Acid in a State-Operated Psychiatric Hospital." Journal of Pharmacy Technology 11, no. 2 (1995): 55–59. http://dx.doi.org/10.1177/875512259501100210.

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Objective: To examine the prescribing of mood stabilizers (lithium, carbamazepine, and valproic acid) in a 500-bed state-operated psychiatric hospital in New York. Method: All 129 inpatients receiving mood stabilizers were identified and their medical records reviewed using a standardized drug use evaluation form. Diagnosis, other indications, and prior experience with mood stabilizers were examined, as well as outcome and adverse effects. Results: Approximately one-quarter of the inpatient population received a mood stabilizer. The frequency of carbamazepine use exceeded the use of lithium, w
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Sonbol, Heba, Hager Ebrahim, Monika Malak, et al. "Application of a Small Protein-Coated Column to Trap, Extract and Enrich Carbamazepine Directly from Human Serum for Direct Chromatographic Analysis." Separations 10, no. 2 (2023): 71. http://dx.doi.org/10.3390/separations10020071.

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An automated solid phase extraction (SPE) protocol to determine carbamazepine in human serum has been developed and validated using a simple, rabid and sensitive liquid chromatography-based bio-analytical method. Extraction of carbamazepine was carried out using an on-line SPE tool of a short protein-coated (PC) ODS silica pre-column (PC-ODS-pre-column) and phosphate buffer saline (PBS) with a pH of 7.4 as an extraction solvent. There are two distinct chromatographic modes used by PC-ODS-pre-column. While carbamazepine trapping required reversed-phase liquid chromatography, proteins were extra
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Damor, Rahul R., Amita R. Kubavat, and Kiran G. Piparva. "Drug reaction with eosinophilia and systemic symptom induced by carbamazepine: a case report." International Journal of Basic & Clinical Pharmacology 8, no. 5 (2019): 1115. http://dx.doi.org/10.18203/2319-2003.ijbcp20191610.

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Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a severe, potentially life-threatening acute adverse drug reaction (ADR), typically characterized by a long latency period (2-6 weeks to 3 months) from drug exposure. DRESS syndrome is defined by the presence of fever, cutaneous eruption, lymphadenopathy, systemic or asymptomatic internal organ involvement (e.g. Hepatitis, carditis, interstitial nephritis, interstitial pneumonitis, etc.) and haematological abnormalities, mainly leucocytosis, eosinophilia and sometimes atypical lymphocytosis. There are around 50 culprit d
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&NA;. "Carbamazepine see Lithium/carbamazepine." Reactions Weekly &NA;, no. 303 (1990): 4. http://dx.doi.org/10.2165/00128415-199003030-00007.

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Turner, Patricia V., and Kenneth W. Renton. "The interaction between carbamazepine and erythromycin." Canadian Journal of Physiology and Pharmacology 67, no. 6 (1989): 582–86. http://dx.doi.org/10.1139/y89-093.

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Erythromycin has been reported to interact with the anticonvulsant, carbamazepine, in both children and adults. Toxic serum levels of carbamazepine are observed within 24 h of antibiotic administration, suggesting a mechanism not previously described for other erythromycin-based drug interactions. In rats erythromycin significantly depressed the elimination of carbamazepine in animals induced with carbamazepine for 4 days but had no effect on carbamazepine elimination in noninduced animals. Although the in vitro metabolism of carbamazepine to its epoxide by hepatic microsomes prepared from non
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&NA;. "Carbamazepine." Reactions Weekly &NA;, no. 1384 (2012): 16. http://dx.doi.org/10.2165/00128415-201213840-00058.

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&NA;. "Carbamazepine." Reactions Weekly &NA;, no. 1386 (2012): 14. http://dx.doi.org/10.2165/00128415-201213860-00047.

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&NA;. "Carbamazepine." Reactions Weekly &NA;, no. 1389 (2012): 15. http://dx.doi.org/10.2165/00128415-201213890-00046.

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&NA;. "Carbamazepine." Reactions Weekly &NA;, no. 1391 (2012): 15. http://dx.doi.org/10.2165/00128415-201213910-00052.

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Dissertations / Theses on the topic "Carbamazepine"

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Webster, Donald Shaw. "Studies of carbamazepine metabolism." Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/27680.

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The objective of this study was to examine aspects of carbamazepine metabolism, in order to contribute to a long term goal of a thorough examination of how the metabolism of carbamazepine is influenced by other drugs. The first set of experiments were designed with the intent of determining values for the pharmacokinetic parameters of carbamazepine metabolism in male New Zealand white rabbits. Values were obtained for t[sub max] (60-90 min), t[sub ½](90-122 min), clearance (46.2-142.4 ml/min/kg), and the elimination constant (0.0057-0.0077 min⁻¹) in five test cases. In the remainder of cases,
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Amore, Benny Michael. "Mechanism of carbamazepine teratogenicity /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/7939.

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VASSEUR, ROSINE. "La carbamazepine : indications en psychiatrie." Clermont-Ferrand 1, 1988. http://www.theses.fr/1988CLF11039.

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Terra, Luciana Assis 1988. "Avaliação de transformação polimórfica em comprimidos do fármaco carbamazepina por espectroscopia de imagem no infravermelho próximo e ferramentas quimiométricas." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249298.

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Orientador: Ronei Jesus Poppi<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Química<br>Made available in DSpace on 2018-08-22T20:20:45Z (GMT). No. of bitstreams: 1 Terra_LucianaAssis_M.pdf: 5662002 bytes, checksum: 969f678029bf9ac1f5d8f5fadf9727f9 (MD5) Previous issue date: 2013<br>Resumo: A Espectroscopia de Imagem na região do Infravermelho Próximo juntamente com ferramentas quimiométricas foi utilizada para estudar a transformação polimórfica do fármaco carbamazepina (forma III para forma I) em formulações farmacêuticas do comprimido, geradas por aquecimento.
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Marlot, Philippe. "In vitro evaluation of cytotoxicity caused by carbamazepine and its metabolites in association to carbamazepine-induced hypersensitivity reactions." Thesis, University of Liverpool, 2014. http://livrepository.liverpool.ac.uk/2025988/.

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Carbamazepine (CBZ), an anticonvulsant and mood-stabilising drug, is known to cause delayed type hypersensitivity reactions. These reactions occur only in a minority of patients treated with the drug, but often result in severe clinical outcomes. Although an association between CBZ-induced hypersensitivity reactions and HLA alleles has been demonstrated, the underlying mechanism(s) of toxicity are poorly understood. Cell death caused by CBZ and one of its metabolites, 9-acridinecarboxaldehyde (9-AC) was investigated. CBZ did not show cytotoxic effects in concentrations ranging from sub-therape
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Alfirevic, Ana. "Molecular aspects of carbamazepine-induced hypersensitivity reactions." Thesis, University of Liverpool, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.421067.

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Wurden, Colleen J. "Metabolism of carbamazepine and inhibitory drug interactions /." Thesis, Connect to this title online; UW restricted, 2000. http://hdl.handle.net/1773/7977.

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Martins, Armando Carvalho de Oliveira. "Processo oxidativo avançado UV/H2O2 na oxidação da carbamazepina : avaliação por ensaios respirometricos e ecotoxicologicos." [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/257867.

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Orientador: Alexandre Nunes Ponezi<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia Civil, Arquitetura e Urbanismo<br>Made available in DSpace on 2018-08-13T11:19:54Z (GMT). No. of bitstreams: 1 Martins_ArmandoCarvalhodeOliveira_M.pdf: 1218959 bytes, checksum: 89c4972bf88120caa1add6b7b1eb515a (MD5) Previous issue date: 2009<br>Resumo: O efeito da poluição é resultado inerente da ocupação humana com grande impacto ao ambiente. Um problema atual é a contaminação dos corpos d'água com produtos de origem industrial, agrícola e produtos de origem farmacológic
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Panesar, Sukhbinder Kaur. "The effect of carbamazepine on valproic acid metabolism." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26511.

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Modifications to the GCMS assay for valproic acid and 12 metabolites were attempted with respect to internal standards and derivatizing reagents. Four new internal standards, octanoic acid and 2-methylglutaric acid for analysis of VPA and metabolites and hexanoic acid and di-ռ-butylacetic acid for the analysis of hexadeuterated VPA and metabolites were used. Two new derivatizing reagents, MSTFA and MTBSTFA, were tested as alternatives to the reagent previously used. TMS (MSTFA) and tBDMS derivatives were compared with respect to sensitivity, stability, and chromatographic time. The derivative
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Yip, V. L. M. "Carbamazepine hypersensitivity : linking metabolism to the immune response." Thesis, University of Liverpool, 2016. http://livrepository.liverpool.ac.uk/3002243/.

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Carbamazepine (CBZ) is an effective antiepileptic drug but has been associated with hypersensitivity reactions in up to 10% of patients. These reactions range from mild maculopapular exanthema to life-threatening conditions such as Stevens-Johnson syndrome and toxic epidermal necrolysis. The identification of CBZ-specific T cells and strong associations with specific human leukocyte antigen alleles provide evidence for immunological involvement. CBZ is extensively metabolised and forms several reactive metabolites. The aim of this thesis was to investigate the complex relationships between CBZ
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Books on the topic "Carbamazepine"

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M, Emrich H., Schiwy W, and Silverstone Trevor, eds. Carbamazepine and oxcarbazepine in psychiatry. Clinical Neuroscience Publishers, 1990.

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Medenwald, Janet R. Carbamazepine and manic depression : a guide. Lithium Information Center/Dean Foundation for Health, Research and Education, 1996.

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Internationales Carbamazepin Slow-Release Symposium (2nd 1986 Frankfurt am Main). 2. Internationales Carbamazepin Slow-Release Symposium, Frankfurt am Main, Dezember 1986. W. Zuckschwerdt, 1988.

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Greil, Waldemar. Manic depressive illness: Therapy with carbamazepine : for patients, relatives and therapists. Thieme, 1996.

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McDermott, Elaine Elizabeth. Inositol lipid hydrolysis in the rat hippocampus: Effects of the anticonvulsant carbamazepine. University of Birmingham, 1989.

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Bengt, Sternebring, ed. Carbamazepine in the treatment of alcoholics: Workshop, Mariehamn, Finland, October 3-5, 1985. Universitetsforlaget, 1987.

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Johnson, Robert D. False carbamazepine positives due to 10,11-dihydro-10-hydroxycarbamazepine breakdown in the GC/MS injector port. Federal Aviation Administration, Office of Aerospace Medicine, 2010.

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Parker, Philip M., and James N. Parker. Tegretol: A medical dictionary, bibliography, and annotated research guide to internet references. ICON Health Publications, 2004.

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Kiel, Universität, ed. Zur Effizienz extrakorporaler Detoxikationsverfahren bei Carbamazepin- und Valproinsäurevergiftungen. [s.n.], 1997.

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Cavanna, Andrea E. Carbamazepine, oxcarbazepine, and eslicarbazepine. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198791577.003.0003.

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Carbamazepine is a first-generation antiepileptic drug characterized by a good range of antiepileptic indications, with acceptable risk of interactions in polytherapy. Carbamazepine has a very good behavioural tolerability profile and is in widespread psychiatric use (indication for bipolar disorder—acute mania). Oxcarbazepine and eslicarbazepine are carbamazepine derivatives. Oxcarbazepine is a second-generation antiepileptic drug characterized by a good range of antiepileptic indications, with acceptable risk of interactions in polytherapy. Like carbamazepine, oxcarbazepine has a very good b
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Book chapters on the topic "Carbamazepine"

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Maxwell, Robert A., and Shohreh B. Eckhardt. "Carbamazepine." In Drug Discovery. Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0469-5_15.

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Courtney, John C. "Carbamazepine." In Encyclopedia of Clinical Neuropsychology. Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_1635.

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Courtney, John C., and Efrain Antonio Gonzalez. "Carbamazepine." In Encyclopedia of Clinical Neuropsychology. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56782-2_1635-2.

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Gonzalez, Efrain Antonio. "Carbamazepine." In Encyclopedia of Clinical Neuropsychology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-56782-2_1635-3.

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Gonzalez, Efrain Antonio. "Carbamazepine." In Encyclopedia of Clinical Neuropsychology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_1635.

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Hoyer, Daniel, Eric P. Zorrilla, Pietro Cottone, et al. "Carbamazepine." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_1767.

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Patsalos, P. N. "Carbamazepine." In Antiepileptic Drug Interactions. Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-2434-4_2.

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Patsalos, P. N. "Carbamazepine." In Antiepileptic Drug Interactions. Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-2434-4_29.

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Panayiotopoulos, C. P. "Carbamazepine." In Antiepileptic Drugs, Pharmacopoeia. Springer London, 2010. http://dx.doi.org/10.1007/978-0-85729-012-0_3.

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Dickinson, R. G., M. J. Eadie, and E. J. E. Vajda. "Carbamazepine." In Antiepileptic Drugs. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60072-2_10.

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Conference papers on the topic "Carbamazepine"

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K, Venkata Ramana, Suman Polaki, Rabi Prasad B, Aswini Kumar M, Mohanababu Ch, and Sravani M. "AI and IoT-Enhanced Laccase-Catalyzed Degradation of Diclofenac and Carbamazepine in Wastewater Treatment." In 2024 2nd International Conference on Signal Processing, Communication, Power and Embedded System (SCOPES). IEEE, 2024. https://doi.org/10.1109/scopes64467.2024.10990969.

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Pino, Esteban J., Francisca Pucheu, Fabian Alvarado, et al. "Carbamazepine Biosensor Development for Epilepsy Patient Screening." In 2021 43rd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC). IEEE, 2021. http://dx.doi.org/10.1109/embc46164.2021.9629901.

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Bayer, A., E. Zrenner, H. J. Thiel, S. Ried, and D. Schmidt. "Early detection of anticonvulsant drug toxicity by colour vision tests." In Noninvasive Assessment of the Visual System. Optica Publishing Group, 1991. http://dx.doi.org/10.1364/navs.1991.md10.

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Phenytoin and Carbamazepine, especially in combination or after repeated exposure to toxic blood concentrations, can produce neurological and mental syndroms. Possible mechanisms of impaired neurological and mental function include neuronal damage, or disturbance of folic acid, monoamine or hormonal metabolism. Phenytoin and Carbamazepine may also impair the ocular system. The most common symptoms are diplopia, nystagmus and blurred vision. Cerebellar or vestibulo-ocular dysfunction is suspected as mechanism of these ocular adverse effects.
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Ramle, Noor Ashila, Syarifah Abd Rahim, Nornizar Anuar, and Omar El-Hadad. "Solubility of carbamazepine co-crystals in ethanolic solution." In 3RD INTERNATIONAL CONFERENCE ON CHEMICAL MATERIALS AND PROCESS (ICCMP 2017). Author(s), 2017. http://dx.doi.org/10.1063/1.5000468.

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Mizner, A. M., M. Bahr, A. Gordon, and D. Speredelozzi. "The Paradoxical Effect: Carbamazepine Overdose Leading to Seizures." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a2925.

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Pajander, Jari, Alexia Rensonnet, Marin Øvergård, et al. "Polymorphic transition of carbamazepine during hot melt processing." In The 2nd Electronic Conference on Pharmaceutical Sciences. MDPI, 2012. http://dx.doi.org/10.3390/ecps2012-00815.

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Hussein, Sama Ali, Abdulmonaim Hamad Al-Samarrai, and Liqaa Hussein Alwan. "Spectroscopic study of carbamazepine on a new nanomaterial." In 1ST SAMARRA INTERNATIONAL CONFERENCE FOR PURE AND APPLIED SCIENCES (SICPS2021): SICPS2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0122477.

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Smiljanić, Danijela, Aleksandra Daković, Milena Obradović, et al. "CARBAMAZEPINE ADSORPTION BY PROMISSING HYDROPHOBIC SURFACTANT-CLAY COMPOSITES." In 17th International Conference on Fundamental and Applied Aspects of Physical Chemistry. Society of Physical Chemists of Serbia, 2024. https://doi.org/10.46793/phys.chem24ii.491s.

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In this study, two surfactants, primary amine dodecylamine (D) and di(hydrogenated tallow)dimethylammonium chloride known under the trade name Arquad®2HT-75 (A) were used to modify bentonite in amounts equivalent to 50% and 100% of bentonite`s cationic exchange capacity. For prepared composites static water contact angle and true density were maeasured. Obtained composites were tested as adsorbents for an anticonvulsant drug – carbamazepine (CARB). The results of the contact angle measurements confirmed that the modification of the starting material changed its surface properties from hydrophi
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Fiter, R. J., and T. Tong. "Covid Confusion: A Case of Paxlovid Induced Carbamazepine Toxicity." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a5695.

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Yuksek, Gulten, Lounes Haroune, Didem Okutman Tas, and Hubert Cabana. "Laccase-Mediator System for the Elimination of Carbamazepine and Atrazine." In International Conference of Recent Trends in Environmental Science and Engineering. Avestia Publishing, 2017. http://dx.doi.org/10.11159/rtese17.126.

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Reports on the topic "Carbamazepine"

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Owens, J. E., A. K. Vu, and B. K. Esser. California GAMA Special Study: Analysis of Carbamazepine, Oxcarbazepine and Metabolites as Wastewater Tracers in Water Resource Studies. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/1119929.

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Asenath-Smith, Emily, Emma Ambrogi, Lee Moores, Stephen Newman, and Jonathon Brame. Leveraging chemical actinometry and optical radiometry to reduce uncertainty in photochemical research. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/42080.

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Subtle aspects of illumination sources and their characterization methods can introduce significant uncertainty into the data gathered from light-activated experiments, limiting their reproducibility and technology transition. Degradation kinetics of methyl orange (MO) and carbamazepine (CM) under illumination with TiO₂ were used as a case study for investigating the role of incident photon flux on photocatalytic degradation rates. Valerophenone and ferrioxalate actinometry were paired with optical radiometry in three different illumination systems: xenon arc (XE), tungsten halogen (W-H), and
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