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Potentially toxic serum concentrations of desipramine after discontinuation of valproic acid.
- Source :
-
Brain injury [Brain Inj] 1993 Sep-Oct; Vol. 7 (5), pp. 463-5. - Publication Year :
- 1993
-
Abstract
- Pharmacological interventions in the treatment of various cognitive, behavioural and neurological problems after brain injury often may involve combinations of medications from various drug classes. This carries the implication of potentially new or previously underreported drug interactions. A case report is presented in which a commonly used anticonvulsant drug, valproic acid, and a commonly used antidepressant, desipramine, interacted in such a manner as to cause potentially toxic serum concentrations of desipramine. This case demonstrates the important point that it is not simply the addition of one drug to another that may cause interaction, but the withdrawal of a particular drug which may then adversely impact the remaining drug regimen.
- Subjects :
- Adult
Clorazepate Dipotassium administration & dosage
Clorazepate Dipotassium pharmacokinetics
Depressive Disorder blood
Desipramine administration & dosage
Desipramine pharmacokinetics
Dose-Response Relationship, Drug
Drug Therapy, Combination
Epilepsy, Post-Traumatic blood
Female
Head Injuries, Closed blood
Humans
Neurocognitive Disorders blood
Valproic Acid administration & dosage
Valproic Acid pharmacokinetics
Depressive Disorder drug therapy
Desipramine adverse effects
Epilepsy, Post-Traumatic drug therapy
Head Injuries, Closed complications
Neurocognitive Disorders drug therapy
Substance Withdrawal Syndrome blood
Valproic Acid adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 0269-9052
- Volume :
- 7
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Brain injury
- Publication Type :
- Academic Journal
- Accession number :
- 8401488
- Full Text :
- https://doi.org/10.3109/02699059309029690