Acute Seizures Due to a Probable Interaction Between Valproic Acid and Meropenem

OBJECTIVE: To report a probable interaction between meropenem and valproic acid that resulted in the development of epileptic seizures. CASE SUMMARY: A 21-year-old woman presented to our emergency department because of a new-onset, generalized tonic—clonic seizure and was admitted to the intensive c...

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Veröffentlicht in:The Annals of pharmacotherapy 2005-03, Vol.39 (3), p.533-537
Hauptverfasser: Coves-Orts, Francisco Javier, Borras-Blasco, Joaquin, Navarro-Ruiz, Andres, Murcia-Lopez, Ana, Palacios-Ortega, Francisco
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container_end_page 537
container_issue 3
container_start_page 533
container_title The Annals of pharmacotherapy
container_volume 39
creator Coves-Orts, Francisco Javier
Borras-Blasco, Joaquin
Navarro-Ruiz, Andres
Murcia-Lopez, Ana
Palacios-Ortega, Francisco
description OBJECTIVE: To report a probable interaction between meropenem and valproic acid that resulted in the development of epileptic seizures. CASE SUMMARY: A 21-year-old woman presented to our emergency department because of a new-onset, generalized tonic—clonic seizure and was admitted to the intensive care unit. Treatment with valproic acid 1000 mg as a continuous intravenous infusion over 24 hours was initiated. On day 6, the serum concentration of valproic acid was 52.5 μg/mL. On day 13, treatment with intravenous meropenem 1 g 3 times daily was started. On day 15, when the patient was afebrile, numerous myoclonic episodes occurred involving her arms and face; the serum concentration of valproic acid at that time was 42 μg/mL. The valproic acid dose was increased to 2880 mg. Two days later, a generalized tonic—clonic seizure occurred despite the increased dosage, and the plasma concentration of valproic acid fell to 7 μg/mL. The valproic acid dose was increased the following day to 3600 mg; however, the serum concentrations remained
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CASE SUMMARY: A 21-year-old woman presented to our emergency department because of a new-onset, generalized tonic—clonic seizure and was admitted to the intensive care unit. Treatment with valproic acid 1000 mg as a continuous intravenous infusion over 24 hours was initiated. On day 6, the serum concentration of valproic acid was 52.5 μg/mL. On day 13, treatment with intravenous meropenem 1 g 3 times daily was started. On day 15, when the patient was afebrile, numerous myoclonic episodes occurred involving her arms and face; the serum concentration of valproic acid at that time was 42 μg/mL. The valproic acid dose was increased to 2880 mg. Two days later, a generalized tonic—clonic seizure occurred despite the increased dosage, and the plasma concentration of valproic acid fell to 7 μg/mL. The valproic acid dose was increased the following day to 3600 mg; however, the serum concentrations remained &lt;10 μg/mL. On day 19, based on the results of a blood culture and the suspicion of an interaction between meropenem and valproic acid, meropenem therapy was suspended. The serum concentration of valproic acid was 52.4 μg/mL on day 27. Three days later, the patient was asymptomatic and was discharged. DISCUSSION: Coadministration of valproic acid and other drugs that are metabolized by the hepatic cytochrome P450 isoenzyme system can lead to clinically relevant interactions by induction or inhibition of enzymes in shared metabolic pathways. In view of studies in experimental models, the interaction between carbapenem antibiotics and valproic acid is at least possible. Use of the Naranjo probability scale indicated a probable relationship between acute seizures and a meropenem—valproic acid interaction in this patient. CONCLUSIONS: This case report provides strong evidence for an interaction between valproic acid and meropenem. Clinicians should be aware of this potential interaction that may be associated with a serious adverse effect as the result of the decrease of the valproic acid serum concentrations.</description><identifier>ISSN: 1060-0280</identifier><identifier>EISSN: 1542-6270</identifier><identifier>DOI: 10.1345/aph.1E358</identifier><identifier>PMID: 15701769</identifier><identifier>CODEN: APHRER</identifier><language>eng</language><publisher>Los Angeles, CA: Harvey Whitney Books</publisher><subject>Acute Disease ; Adult ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - metabolism ; Anticonvulsants - adverse effects ; Anticonvulsants - blood ; Anticonvulsants. Antiepileptics. Antiparkinson agents ; Biological and medical sciences ; Drug Interactions ; Epilepsy - chemically induced ; Female ; Humans ; Infusions, Intravenous ; Medical sciences ; Neuropharmacology ; Pharmacology. 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CASE SUMMARY: A 21-year-old woman presented to our emergency department because of a new-onset, generalized tonic—clonic seizure and was admitted to the intensive care unit. Treatment with valproic acid 1000 mg as a continuous intravenous infusion over 24 hours was initiated. On day 6, the serum concentration of valproic acid was 52.5 μg/mL. On day 13, treatment with intravenous meropenem 1 g 3 times daily was started. On day 15, when the patient was afebrile, numerous myoclonic episodes occurred involving her arms and face; the serum concentration of valproic acid at that time was 42 μg/mL. The valproic acid dose was increased to 2880 mg. Two days later, a generalized tonic—clonic seizure occurred despite the increased dosage, and the plasma concentration of valproic acid fell to 7 μg/mL. The valproic acid dose was increased the following day to 3600 mg; however, the serum concentrations remained &lt;10 μg/mL. On day 19, based on the results of a blood culture and the suspicion of an interaction between meropenem and valproic acid, meropenem therapy was suspended. The serum concentration of valproic acid was 52.4 μg/mL on day 27. Three days later, the patient was asymptomatic and was discharged. DISCUSSION: Coadministration of valproic acid and other drugs that are metabolized by the hepatic cytochrome P450 isoenzyme system can lead to clinically relevant interactions by induction or inhibition of enzymes in shared metabolic pathways. In view of studies in experimental models, the interaction between carbapenem antibiotics and valproic acid is at least possible. Use of the Naranjo probability scale indicated a probable relationship between acute seizures and a meropenem—valproic acid interaction in this patient. CONCLUSIONS: This case report provides strong evidence for an interaction between valproic acid and meropenem. Clinicians should be aware of this potential interaction that may be associated with a serious adverse effect as the result of the decrease of the valproic acid serum concentrations.</description><subject>Acute Disease</subject><subject>Adult</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - metabolism</subject><subject>Anticonvulsants - adverse effects</subject><subject>Anticonvulsants - blood</subject><subject>Anticonvulsants. Antiepileptics. Antiparkinson agents</subject><subject>Biological and medical sciences</subject><subject>Drug Interactions</subject><subject>Epilepsy - chemically induced</subject><subject>Female</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Seizures - drug therapy</subject><subject>Thienamycins - adverse effects</subject><subject>Thienamycins - metabolism</subject><subject>Valproic Acid - adverse effects</subject><subject>Valproic Acid - blood</subject><issn>1060-0280</issn><issn>1542-6270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE1P4zAQhi0EogX2sH9g5QtIHAL-iJ36WD52FwkE0n5crYk9oanSJLITRfDr8W4r9cJp5vDofWceQr5ydsVlrq6hX13xe6kWB2TOVS4yLQp2mHamWcbEgs3ISYxrxpjhwhyTGVcF44U2c_KydOOA9BfW72PASO9GpENHgb6EroSyQfrQDhjADXXX0hscJsSW_oWmD13t6NLVnkLr6ROGrscWN2fkqIIm4pfdPCV_vt__vv2ZPT7_eLhdPmYuz9mQSa-FVwunsVRamYobIdO1AgFMrkoPQvPccO8Ko50QGmQFzBtRKV8UKLQ8JZfbXBe6GANWtg_1BsKb5cz-s2KTFfvfSmK_bdl-LDfo9-ROQwLOdwBEB00VoHV13HPpwmIhWOIutlyEV7Trbgxt-vHTxl3gqn5dTXVAGzfQNKmf22mapLHSKinlB702gpk</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Coves-Orts, Francisco Javier</creator><creator>Borras-Blasco, Joaquin</creator><creator>Navarro-Ruiz, Andres</creator><creator>Murcia-Lopez, Ana</creator><creator>Palacios-Ortega, Francisco</creator><general>Harvey Whitney Books</general><general>SAGE Publications</general><general>Whitney</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050301</creationdate><title>Acute Seizures Due to a Probable Interaction Between Valproic Acid and Meropenem</title><author>Coves-Orts, Francisco Javier ; Borras-Blasco, Joaquin ; Navarro-Ruiz, Andres ; Murcia-Lopez, Ana ; Palacios-Ortega, Francisco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-3d62d58c6eb5659f19230602eaa945bda261491dc796c226a3fa0d92f5d77e263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acute Disease</topic><topic>Adult</topic><topic>Anti-Bacterial Agents - adverse effects</topic><topic>Anti-Bacterial Agents - metabolism</topic><topic>Anticonvulsants - adverse effects</topic><topic>Anticonvulsants - blood</topic><topic>Anticonvulsants. Antiepileptics. Antiparkinson agents</topic><topic>Biological and medical sciences</topic><topic>Drug Interactions</topic><topic>Epilepsy - chemically induced</topic><topic>Female</topic><topic>Humans</topic><topic>Infusions, Intravenous</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Seizures - drug therapy</topic><topic>Thienamycins - adverse effects</topic><topic>Thienamycins - metabolism</topic><topic>Valproic Acid - adverse effects</topic><topic>Valproic Acid - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Coves-Orts, Francisco Javier</creatorcontrib><creatorcontrib>Borras-Blasco, Joaquin</creatorcontrib><creatorcontrib>Navarro-Ruiz, Andres</creatorcontrib><creatorcontrib>Murcia-Lopez, Ana</creatorcontrib><creatorcontrib>Palacios-Ortega, Francisco</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The Annals of pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coves-Orts, Francisco Javier</au><au>Borras-Blasco, Joaquin</au><au>Navarro-Ruiz, Andres</au><au>Murcia-Lopez, Ana</au><au>Palacios-Ortega, Francisco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute Seizures Due to a Probable Interaction Between Valproic Acid and Meropenem</atitle><jtitle>The Annals of pharmacotherapy</jtitle><addtitle>Ann Pharmacother</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>39</volume><issue>3</issue><spage>533</spage><epage>537</epage><pages>533-537</pages><issn>1060-0280</issn><eissn>1542-6270</eissn><coden>APHRER</coden><abstract>OBJECTIVE: To report a probable interaction between meropenem and valproic acid that resulted in the development of epileptic seizures. CASE SUMMARY: A 21-year-old woman presented to our emergency department because of a new-onset, generalized tonic—clonic seizure and was admitted to the intensive care unit. Treatment with valproic acid 1000 mg as a continuous intravenous infusion over 24 hours was initiated. On day 6, the serum concentration of valproic acid was 52.5 μg/mL. On day 13, treatment with intravenous meropenem 1 g 3 times daily was started. On day 15, when the patient was afebrile, numerous myoclonic episodes occurred involving her arms and face; the serum concentration of valproic acid at that time was 42 μg/mL. The valproic acid dose was increased to 2880 mg. Two days later, a generalized tonic—clonic seizure occurred despite the increased dosage, and the plasma concentration of valproic acid fell to 7 μg/mL. The valproic acid dose was increased the following day to 3600 mg; however, the serum concentrations remained &lt;10 μg/mL. On day 19, based on the results of a blood culture and the suspicion of an interaction between meropenem and valproic acid, meropenem therapy was suspended. The serum concentration of valproic acid was 52.4 μg/mL on day 27. Three days later, the patient was asymptomatic and was discharged. DISCUSSION: Coadministration of valproic acid and other drugs that are metabolized by the hepatic cytochrome P450 isoenzyme system can lead to clinically relevant interactions by induction or inhibition of enzymes in shared metabolic pathways. In view of studies in experimental models, the interaction between carbapenem antibiotics and valproic acid is at least possible. Use of the Naranjo probability scale indicated a probable relationship between acute seizures and a meropenem—valproic acid interaction in this patient. CONCLUSIONS: This case report provides strong evidence for an interaction between valproic acid and meropenem. Clinicians should be aware of this potential interaction that may be associated with a serious adverse effect as the result of the decrease of the valproic acid serum concentrations.</abstract><cop>Los Angeles, CA</cop><pub>Harvey Whitney Books</pub><pmid>15701769</pmid><doi>10.1345/aph.1E358</doi><tpages>5</tpages></addata></record>
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subjects Acute Disease
Adult
Anti-Bacterial Agents - adverse effects
Anti-Bacterial Agents - metabolism
Anticonvulsants - adverse effects
Anticonvulsants - blood
Anticonvulsants. Antiepileptics. Antiparkinson agents
Biological and medical sciences
Drug Interactions
Epilepsy - chemically induced
Female
Humans
Infusions, Intravenous
Medical sciences
Neuropharmacology
Pharmacology. Drug treatments
Seizures - drug therapy
Thienamycins - adverse effects
Thienamycins - metabolism
Valproic Acid - adverse effects
Valproic Acid - blood
title Acute Seizures Due to a Probable Interaction Between Valproic Acid and Meropenem
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