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Reactions 1460, p9 - 13 Jul 2013 S Amoxicillin/clavulanic acid/ oxcarbazepine Liver injury and elevation of liver enzymes: case report A 23-year-old woman developed drug-induced liver injury while receiving oxcarbazepine, and later a transitory elevation of liver enzymes while receiving amoxicillin/clavulanic acid. The woman experienced partial complex seizures with oral automatisms and change in consciousness 1 month postpartum. She was diagnosed with localisation-related epilepsy, and on 19 April 2007, she started oxcarbazepine 300mg twice daily [route not stated] for seizure control. Of note, previous baseline investigations had shown borderline elevated AST and GGT values. Tests on 4 May revealed significantly elevated liver enzymes, and 10 days later she was hospitalised; at this time, her AST, ALT and GGT upper limits of normal values were 5.0, 8.9 and 6.1, respectively. She reported appetite loss and fatigue. Oxcarbazepine-induced liver injury was suspected. On 15 May 2007, oxcarbazepine was withdrawn, and the woman started gabapentin. Her liver enzyme abnormalities continued for some time, then gradually improved. Tests showed slight lymphocytosis, and a liver ultrasound revealed hyperechogenic liver parenchyma. She subsequently achieved good clinical remission. Two years later, she received amoxicillin/clavulanic acid [dosage and route not stated] for acute tonsillopharyngitis, and again developed a transitory elevation of liver enzymes; her AST, ALT and GGT values were 1.6, 3.7 and 2.3, respectively [duration of treatment to reaction onset and outcome not stated]. Author comment: "According to the [Council for International Organisations of Medical Sciences (CIOMS)] scale, causal relationship between the [oxcarbazepine] intake and hepatotoxicity would be probable (score 8). Further association with pregnancy, as one of the risk factors for drug induced liver injury, would increase this causal relationship in our patient to highly probable or definite (score 9)." Planjar-Prvan M, et al. Acute oxcarbazepine-induced hepatotoxicity in a patient susceptible to developing drug-induced liver injury. Collegium Antropologicum 37: 281-4, No. 1, Apr 2013. Available from: URL: http://hrcak.srce.hr/ index.php?show=toc&id%5Fbroj=8074 - Croatia 803089738 1 Reactions 13 Jul 2013 No. 1460 0114-9954/13/1460-0001/$14.95 Adis © 2013 Springer International Publishing AG. All rights reserved

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Page 1: Amoxicillin/clavulanic acid/oxcarbazepine

Reactions 1460, p9 - 13 Jul 2013

SAmoxicillin/clavulanic acid/oxcarbazepine

Liver injury and elevation of liver enzymes: casereport

A 23-year-old woman developed drug-induced liver injurywhile receiving oxcarbazepine, and later a transitory elevationof liver enzymes while receiving amoxicillin/clavulanic acid.

The woman experienced partial complex seizures with oralautomatisms and change in consciousness 1 monthpostpartum. She was diagnosed with localisation-relatedepilepsy, and on 19 April 2007, she started oxcarbazepine300mg twice daily [route not stated] for seizure control. Ofnote, previous baseline investigations had shown borderlineelevated AST and GGT values. Tests on 4 May revealedsignificantly elevated liver enzymes, and 10 days later she washospitalised; at this time, her AST, ALT and GGT upper limits ofnormal values were 5.0, 8.9 and 6.1, respectively. Shereported appetite loss and fatigue. Oxcarbazepine-inducedliver injury was suspected.

On 15 May 2007, oxcarbazepine was withdrawn, and thewoman started gabapentin. Her liver enzyme abnormalitiescontinued for some time, then gradually improved. Testsshowed slight lymphocytosis, and a liver ultrasound revealedhyperechogenic liver parenchyma. She subsequently achievedgood clinical remission. Two years later, she receivedamoxicillin/clavulanic acid [dosage and route not stated] foracute tonsillopharyngitis, and again developed a transitoryelevation of liver enzymes; her AST, ALT and GGT valueswere 1.6, 3.7 and 2.3, respectively [duration of treatment toreaction onset and outcome not stated].

Author comment: "According to the [Council forInternational Organisations of Medical Sciences (CIOMS)]scale, causal relationship between the [oxcarbazepine] intakeand hepatotoxicity would be probable (score 8). Furtherassociation with pregnancy, as one of the risk factors for druginduced liver injury, would increase this causal relationship inour patient to highly probable or definite (score 9)."Planjar-Prvan M, et al. Acute oxcarbazepine-induced hepatotoxicity in a patientsusceptible to developing drug-induced liver injury. Collegium Antropologicum 37:281-4, No. 1, Apr 2013. Available from: URL: http://hrcak.srce.hr/index.php?show=toc&id%5Fbroj=8074 - Croatia 803089738

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Reactions 13 Jul 2013 No. 14600114-9954/13/1460-0001/$14.95 Adis © 2013 Springer International Publishing AG. All rights reserved