Autopsic Examination Case of Levomepromazine Toxicity
Journal of Clinical Toxicology

Journal of Clinical Toxicology
Open Access

ISSN: 2161-0495

+44 1478 350008

Case Report - (2016) Volume 6, Issue 1

Autopsic Examination Case of Levomepromazine Toxicity

Satoshi Furukawa* and Masahito Hitosugi
Department of Legal Medicine, Shiga University of Medical Science, Setatsukinowa, Otsu City, Shiga 520-2192, Japan
*Corresponding Author: Satoshi Furukawa, Department of Legal Medicine, Shiga University of Medical Science, Setatsukinowa, Otsu City, Shiga 520-2192, Japan, Tel: +81-77-548-2200 Email:


Levomepromazine is an antipsychotic drug that is used clinically for a variety of distressing symptoms. A 39 year old female was found dead in the living room. A full autopsy was performed approximately 30 h after death. Analysis of available biological fluids was carried out. The concentration for levomepromazine was 3.0 g/ml in blood and 380 g/ml in stomach contents. We clearly showed the cause of death was ascribed to levomepromazine overdose.

Keywords: Levomepromazine, Overdose, Autopsy


Analgesics, antiemetics, sedatives and anxiolytics titrated to the individual patient’s level of need should be prescribed and any medication, which is not essential for symptom control, discontinued. Drugs administration is preferably via subcutaneous routes, and the amount of patient manipulation related to medication delivery, reduced to a minimum. In severe cases, where patients experience an unbearable and/or refractory symptom burden, palliative sedation therapy may be considered as an important and necessary therapeutic intervention [1,2]. The aliphatic phenothiazine is a neuroleptic with low antipsychotic potency first used in psychiatry for the treatment of schizophrenia [3]. Levomepromazine acts as an antagonist at histamine type 1, muscarinic-cholinergic, dopaminergic 2, alpha-1 adrenoceptor and 5HT-2 receptors [4,5], and due to a half-life 15-30 hours makes once daily administration practicable. It can be administered subcutaneously, intravenously or orally. Known adverse drug effects include postural hypotension, skin irritation, drowsiness, dry mouth, dystonia, neuroleptic malignant syndrome, Parkinsonism and epilepsy by lowering the seizure threshold [6-8]. Adverse effects appear associated with higher doses and rapid introduction of the drug [9-11]. We present the documented case of a fatality caused by an overdose of levomepromazine.

Case Report

The deceased was a 39 year old female found dead in the living room. A full autopsy was performed approximately 30 h after death. Autopsy findings showed the congestion at the organ level and pulmonary edema. Cardiac blood and stomach contents were collected for toxicological analysis. All specimens were initially subjected to a thorough qualitative analysis. Screening was performed for basic, acidic, and neutral drugs and volatiles by standard chromatographic methods. The levomepromazine concentration was 3.0 g/ml in blood and 380 g/ml in stomach contents. It was above its therapeutic limit. The flunitrazepam concentration was 0.1 g/ml and 3.3 g/ml, the brotizolam was 0.2 g/ml and 0.6 g/ml, and sodium valproate was 12 g/ml and 30 g/ml respectively. They were within their therapeutic limit (Table 1).


Levomepromazine is a drug with broad-range applicability and effectiveness in the treatment of symptoms had already been demonstrated in a study by Oliver et al. in 1985 [12]. The use of levomepromazine for symptom control has been considered in several published systematic reviews concerning individual symptoms, such as the treatment of nausea and vomiting, breathlessness or sedation [13-15]. Table 1 presents the essential pharmacokinetic data of the drug. Lecomepromazine is predominantly used for the treatment of nausea and vomiting, and for severe delirium or agitation. Actually, sedation was reported as a noted side effect of levomepromazine, whereas subsequent studies in the 1990 turned that side effect into a benefit and started to realize the value of the drug as a part of treatment where sedation was indicated and/or intended [16,17]. Effectiveness of sedation was measured in only some of the papers, mostly subjectively rather than with standardized tools [12,16,18]. There are a large number of papers dealing with the use of levomepromazine in palliative sedation, most of them recommend its use in combination with midazolam or as a second line drug for continuous sedation if midazolam is ineffective [15,16,18-20]. In this case, flunitrazepam, brotizolam and sodium valproate were combinated. Although they were within their therapeutic limit, they might strengthen the effect of levomepromazine by drug-drug interactions.


Levomepromazine is widely used as antipsychotic, anxiolytic, antiemetic and sedative drug. The findings suggest acute toxicity, and the cause of death was ascribed to levomepromazine overdose.


  1. Fainsinger R, MillerMJ, Bruera E, Hanson J, Maceachem T (1991) Symptom control during the last week of life on a palliative care unit. J Palliat Care 7: 5-11.
  2. Cherny NI, Radbruch L; Board of the European Association for Palliative Care (2009) European Association for Palliative Care (EAPC) recommended framework for the use of sedation in palliative care.Palliat Med 23: 581-593.
  3. Sivaraman P, Rattehalli RD, Jayaram MB (2010) Levomepromazine for schizophrenia.Cochrane Database Syst Rev : CD007779.
  4. Hals PA, Hall H, Dahl SG (1988) Muscarinic cholinergic and histamine H1 receptor binding of phenothiazine drug metabolites.Life Sci 43: 405-412.
  5. Lal S, Nair NP, Cecyre D, Quirion R (1993) Levomepromazine receptor binding profile in human brain-implications for treatment-resistant schizophrenia. Acta Psychiatr Scand 87: 380-383.
  6. Harris DG (2010) Nausea and vomiting in advanced cancer.Br Med Bull 96: 175-185.
  7. Eisenchlas JH, Garrigue N, Junin M, De Simone GG (2005) Low-dose levomepromazine in refractory emesis in advanced cancer patients: an open-label study.Palliat Med 19: 71-75.
  8. Langtry HD, Gillis JC, Davis R (1997) Topiramate. A review of its pharmacodynamic and pharmacokinetic properties and clinical efficacy in the management of epilepsy. Drugs 54: 752-773.
  9. Perucca E (1997) A pharmacological and clinical review on topiramate, a new antiepileptic drug.Pharmacol Res 35: 241-256.
  10. MW Jones (1998) Topiramate safety and tolerability. Can J Neurol Sci 25: 513-515.
  11. Oliver DJ (1985) The use of methotrimeprazine in terminal care. Br J Clin Pract 39: 339-340.
  12. Davis MP, Hallerberg G; Palliative Medicine Study Group of the Multinational Association of Supportive Care in Cancer (2010) A systematic review of the treatment of nausea and/or vomiting in cancer unrelated to chemotherapy or radiation.J Pain Symptom Manage 39: 756-767.
  13. Booth S, Moosavi SH, Higginson IJ (2008) The etiology and management of intractable breathlessness in patients with advanced cancer: a systematic review of pharmacological therapy. Nat Clin Pract Oncol 5: 90-100.
  14. Morita T, Bito S, Kurihara Y, Uchitomi Y (2005) Development of a clinical guideline for palliative sedation therapy using the Delphi method.J Palliat Med 8: 716-729.
  15. Chater S, Viola R, Paterson J, Jarvis V (1998) Sedation for intractable distress in the dying--a survey of experts.Palliat Med 12: 255-269.
  16. Stone P, Phillips C, Spruyt O, Waight C (1997) A comparison of the use of sedatives in a hospital support team and in a hospice.Palliat Med 11: 140-144.
  17. Alonso-Babarro A, Varela-Cerdeira M, Torres-Vigil I, Rodríguez-Barrientos R, Bruera E (2010) At-home palliative sedation for end-of-life cancer patients.Palliat Med 24: 486-492.
  18. Mercadante S, Porzio G, Valle A, Fusco F, Aielli F, et al. (2011) Palliative sedation in patients with advanced cancer followed at home: a systematic review.J Pain Symptom Manage 41: 754-760.
  19. LeBon B, Fisher S (2011) Case report: Maintaining and withdrawing long-term invasive ventilation in a patient with MND/ALS in a home setting.Palliat Med 25: 262-265.
Citation: Furukawa S and Hitosugi M (2016) Autopsic Examination Case of Levomepromazine Toxicity. J Clin Toxicol 6:278.

Copyright: © 2016 Furukawa S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.