Case Reports in Psychiatry

Case Reports in Psychiatry / 2011 / Article

Case Report | Open Access

Volume 2011 |Article ID 350417 |

Alan L. Peterson, Robert A. Seegmiller, Libby S. Schindler, "Severe Neuropsychiatric Reaction in a Deployed Military Member after Prophylactic Mefloquine", Case Reports in Psychiatry, vol. 2011, Article ID 350417, 4 pages, 2011.

Severe Neuropsychiatric Reaction in a Deployed Military Member after Prophylactic Mefloquine

Academic Editor: D. E. Dietrich
Received19 Jun 2011
Accepted11 Jul 2011
Published08 Sep 2011


Recent studies of military personnel who have deployed to Iraq and Afghanistan have reported a number of combat-related psychiatric disorders such as posttraumatic stress disorder, depression, and traumatic brain injury. This case report involves a 27-year-old male active-duty US military service member who developed severe depression, psychotic hallucinations, and neuropsychological sequelae following the prophylactic use of the antimalarial medication mefloquine hydrochloride. The patient had a recent history of depression and was taking antidepressant medications at the time of his deployment to the Middle East. Psychiatrists and other health care providers should be aware of the possible neuropsychiatric side effects of mefloquine in deployed military personnel and should consider the use of other medications for malaria prophylaxis in those individuals who may be at increased risk for side effects.

1. Introduction

The stress of military combat can result in a wide array of psychiatric conditions [1]. Posttraumatic stress disorder, depression, and traumatic brain injury are three of the most commonly reported psychiatric conditions reported in studies of multinational military personnel who have served in the wars in Iraq and Afghanistan [24]. Although most combat-related psychiatric conditions are thought to be related to events occurring on the military battlefield, neuropsychiatric reactions can also be related to a number of other deployment-related factors such as environmental exposures [5], chemical warfare agents [6], immunizations [7], and the use of prophylactic medications [8].

Mefloquine was initially developed as a treatment for malaria by the US Army in the 1960s [9]. It was introduced for the treatment of malaria in the late 1970s and became available as a prophylactic drug in 1985. Mefloquine is indicated for the prophylaxis and treatment of Plasmodium vivax and susceptible strains of Plasmodium falciparum. Usual prophylaxis dosing is once weekly starting the week prior to departure to an endemic area and for four weeks following return [10].

There are numerous published case reports [8, 1119] and cohort studies [2024] in the civilian literature of individuals who have experienced neuropsychiatric reactions to the prophylactic use of mefloquine hydrochloride (Lariam). Cohort studies have indicated that the use of mefloquine is associated with an increased risk of depression [2023], central nervous system symptoms [21], and insomnia [24]. One study found that females reported adverse events more frequently than males [20]. Severe neuropsychiatric reactions to mefloquine have primarily been reported in case studies and have included depression [8, 13, 18, 23] and psychosis [8, 12, 1519, 25]. There have also been reports of neuropsychological side effects associated with the prophylactic use of mefloquine, including deficits in orientation, attention, psychomotor speed, and executive, visuospatial, and verbal memory functioning [26].

There have been two randomized double-blind studies of mefloquine [27, 28]. One study included 119 participants and compared mefloquine to atovaquone (250 mg) plus chloroguanide (100 mg) and found that prophylactic use of mefloquine was associated with higher scores on scales measuring depression [27]. In the only published study of US military personnel, 359 Marines were randomized to two prophylactic mefloquine regimens compared with chloroquine [28]. Depressive feelings were noted in two to three times more individuals in the mefloquine groups early in the course of the study and then resolved in most participants as tolerance developed.

The Cochrane Database review includes 516 adverse events published in 136 papers between 1976 and 2000 [29]. However, these adverse events are primarily established through spontaneously reported symptoms rather than through any large-scale surveillance system. Therefore, the authors believe that the reported 1 in 10,000 incidence of neuropsychiatric adverse effects represents a significant underreporting.

The increasing body of literature on the potential for severe neuropsychiatric reactions with the prophylactic use of mefloquine led the Food and Drug Administration (FDA) to release a Safety Alert in September 2002 [30]. This alert states “Larium should not be prescribed for prophylaxis in patients with active depression, a recent history of depression, generalized anxiety disorder, psychosis, or schizophrenia or other major psychiatric disorders, or with a history of convulsions.” Although previous case reports have been published on the neuropsychiatric reactions to mefloquine in civilians, the present case report is the first published report of a significant neuropsychiatric adverse reaction to prophylactic mefloquine in a deployed US military member.

2. Case Presentation

The patient was a 27-year-old male Staff Sergeant with 9 years of active-duty military service in the U.S. Air Force. He was an electronic warfare technician with an excellent service record who successfully supervised 20 military personnel prior to his deployment to an undisclosed location in Southwest Asia. In the six months prior to deployment, he received treatment by both military and civilian physicians for chronic low back pain associated with degenerative disc disease and secondary depression. He was prescribed a variety of medications including acetaminophen and codeine, hydrocodone and acetaminophen, acetaminophen and oxycodone, sertraline, mirtazapine, clonazepam, lorazepam, diazepam, and buspirone. He also participated in outpatient counseling with an Air Force social worker.

Prior to his military deployment, he discontinued all medications except sertraline (200 mg per day) and diazepam (2 mg, as needed). When the patient was medically screened for deployment, he reported he was feeling well enough both physically and emotionally to be deployed. He was subsequently medically cleared for deployment, and shortly thereafter he received his first weekly dose of mefloquine for antimalarial prophylaxis. After arriving in the deployed location, approximately one week later, he took his second dose of mefloquine. Shortly after his second dose, he reported restlessness and sleep disturbances. The following week, after taking his third dose, the patient reported feeling moderately depressed. After taking his fourth weekly dose, he reported becoming very depressed and emotionally labile. His wife verified that he called home about this time and sounded very distraught and could not stop crying. Shortly after his fifth weekly dose, the patient began experiencing florid visual hallucinations, difficulty speaking, vivid nightmares, hypnopompic sleep paralysis, intense feelings of depression with uncontrollable crying, and strong suicidal ideations. He sought medical attention at a deployed medical clinic and was told to discontinue taking the mefloquine. He continued to take sertraline (200 mg per day), and his diazepam was increased from 2 mg as needed to 2–4 mg twice daily to manage his acute emotional distress. He was later found wandering aimlessly on the other side of the deployed base, confused, and disoriented. Over the course of his deployment, the military service member was not exposed to any activity or stressor that might cause traumatic reactions and justify the symptoms recorded.

The patient was subsequently aeromedically evacuated from his deployed location and arrived home a few days later, where his physical presentation and behavior alarmed his spouse. He was initially very quiet, nervous, and tense, displayed significant problems with word finding and speech enunciation, was afraid to go to sleep or be left alone, and was emotionally labile. The patient reported feeling overwhelmed by sensory stimuli and feeling “like a whole rush of stuff going into your brain at one time.” He perspired profusely and complained of being hot even on cold days. He continued to experience occasional visual hallucinations, violent nightmares, and “flashbacks.” He reported that on one occasion, he became enraged and held a chair over his head, as if he was going to throw it at his wife when she did not respond quickly enough after he called her. All of these behaviors were reported to be very atypical for the patient.

He was subsequently admitted to the inpatient psychiatric unit at Wilford Hall Medical Center in San Antonio, Texas, for further evaluation. His behavior on the inpatient psychiatric ward was very labile, ranging from agitated and confrontational, to tearful and shaky, to calm and cooperative. The patient participated in a neuropsychological evaluation over the course of two days, including an extended clinical interview and the administration of a comprehensive eight-hour battery of cognitive and personality tests. He was cooperative and appeared to put forth his best effort throughout the evaluation. His performance on “effort” tests and his scores on validity scales from the Minnesota Multiphasic Personality Inventory-2 were not consistent with symptom exaggeration, inadequate effort, or malingering.

The patient’s neuropsychological evaluation was considered valid. Although his full-scale intelligence quotient (IQ) was in the average range, he displayed significant deficits on certain neuropsychological tests, including moderate to severe impairments on measures of verbal learning, auditory and visual memory, verbal productivity, and upper extremity motor speed and dexterity. Milder impairments were noted on measures of sustained attention and concentration, information processing speed, visuomotor coordination and construction, and grip strength. Personality testing indicated that the patient was moderately depressed, anxious, tense, confused, and socially alienated. He reported a higher than average number of somatic complaints, reflecting his perception that his physical health was failing and his mind was not functioning properly.

3. Discussion

The etiology of severe neuropsychiatric reactions to prophylactic mefloquine is not clear. It has been suggested that it may be related to primary liver damage with secondary thyroid damage [31]. Severe mefloquine-induced neuropsychiatric side effects have also been attributed to a central anticholinergic syndrome [32]. It has been suggested that adverse reactions to mefloquine, including neuropsychiatric reactions, can be potentiated by concomitant ethanol ingestion [33] and by conditions that can lead to mild dehydration such as prolonged air travel, hot or dry conditions, and strenuous physical activity [31]. In the present case study, the patient’s history of depression and the concomitant use of sertraline, diazepam, and mefloquine should be considered factors which may have predisposed him for the severe neuropsychiatric reaction.

Prophylaxis against malaria still has benefits that frequently outweigh the risks, especially for deployed military medical personnel. Since 2001, approximately 2 million US military personnel have deployed to Iraq and Afghanistan, and prophylactic mefloquine continues to be used in some locations [34]. Military medical providers should be aware of the potential for neuropsychiatric reaction with the prophylactic use of mefloquine, especially in patients with a recent history of neuropsychiatric illness (mood disorders, psychotic disorders, or seizure disorders) [35]. In these cases, an alternative antimalarial agent (e.g., doxycycline) might be preferable. Additionally, patients receiving mefloquine should be educated to seek medical attention if they experience anxiety, depression, restlessness, confusion, or irritability. Additional prospective surveillance studies of evaluating the prophylactic use of mefloquine in deployed military personnel are needed.


The views expressed in this paper are solely those of the authors and do not represent the views of or an endorsement by the U.S. Air Force, the Department of Defense, or the U.S. Government.


  1. J. R. Rundell, “Demographics of and diagnoses in operation enduring freedom and operation Iraqi freedom personnel who were psychiatrically evacuated from the theater of operations,” General Hospital Psychiatry, vol. 28, no. 4, pp. 352–356, 2006. View at: Publisher Site | Google Scholar
  2. I. M. Engelhard, M. A. Van Den Hout, J. Weerts, A. Arntz, J. J. C. M. Hox, and R. J. McNally, “Deployment-related stress and trauma in Dutch soldiers returning from Iraq: prospective study,” The British Journal of Psychiatry, vol. 191, pp. 140–145, 2007. View at: Publisher Site | Google Scholar
  3. C. W. Hoge, J. L. Auchterlonie, and C. S. Milliken, “Mental health problems, use of mental health services, and attrition from military service after returning from deployment to Iraq or Afghanistan,” The Journal of the American Medical Association, vol. 295, no. 9, pp. 1023–1032, 2006. View at: Publisher Site | Google Scholar
  4. N. T. Fear, M. Jones, D. Murphy et al., “What are the consequences of deployment to Iraq and Afghanistan on the mental health of the UK armed forces? A cohort study,” The Lancet, vol. 375, no. 9728, pp. 1783–1797, 2010. View at: Publisher Site | Google Scholar
  5. J. P. Engelbrecht, E. V. McDonald, J. A. Gillies, R. K. M. Jayanty, G. Casuccio, and A. W. Gertler, “Characterizing mineral dusts and other aerosols from the Middle East—part 1: ambient sampling,” Inhalation Toxicology, vol. 21, no. 4, pp. 297–326, 2009. View at: Publisher Site | Google Scholar
  6. L. L. Chao, J. C. Rothlind, V. A. Cardenas, D. J. Meyerhoff, and M. W. Weiner, “Effects of low-level exposure to sarin and cyclosarin during the 1991 Gulf war on brain function and brain structure in US veterans,” Neurotoxicology, vol. 31, no. 5, pp. 493–501, 2010. View at: Publisher Site | Google Scholar
  7. H. L. Kelsall, M. R. Sim, A. B. Forbes et al., “Symptoms and medical conditions in Australian veterans of the 1991 Gulf war: relation to immunisations and other Gulf war exposures,” Occupational and Environmental Medicine, vol. 61, no. 12, pp. 1006–1013, 2004. View at: Publisher Site | Google Scholar
  8. A. Dietz and L. Frolich, “Mefloquine-induced paranoid psychosis and subsequent major depression in a 25-year-old student,” Pharmacopsychiatry, vol. 35, no. 5, pp. 200–202, 2002. View at: Publisher Site | Google Scholar
  9. W. D. Tigertt, “The army malaria research program,” Annals of Internal Medicine, vol. 70, no. 1, pp. 150–153, 1969. View at: Google Scholar
  10. Roche Laboratories, “Product information; Lariam ®,” Mefloquine Hydrochloride, Nutley, NJ, USA, 2001. View at: Google Scholar
  11. A. M. J. Croft and M. J. World, “Neuropsychiatric reactions with mefloquine chemoprophylaxis,” The Lancet, vol. 347, no. 8997, p. 326, 1996. View at: Publisher Site | Google Scholar
  12. A. Sowunmi, “Acute psychosis after mefloquine: a case report,” East African Medical Journal, vol. 71, no. 12, pp. 818–820, 1994. View at: Google Scholar
  13. E. Caillon, L. Schmitt, and P. Moron, “Acute depressive symptoms after mefloquine treatment,” American Journal of Psychiatry, vol. 149, no. 5, p. 712, 1992. View at: Google Scholar
  14. P. V. Havaldar and K. D. Mogale, “Mefloquine-induced psychosis,” Pediatric Infectious Disease Journal, vol. 19, no. 2, pp. 166–167, 2000. View at: Google Scholar
  15. R. B. Piening and S. A. Young, “Mefloquine-induced psychosis,” Annals of Emergency Medicine, vol. 27, no. 6, pp. 792–793, 1996. View at: Google Scholar
  16. K. Meszaros, “Acute psychosis caused by mefloquine prophylaxis?” The Canadian Journal of Psychiatry, vol. 41, no. 3, article 196, 1996. View at: Google Scholar
  17. A. Sowunmi, R. A. Adio, A. M. J. Oduola, O. A. T. Ogundahunsi, and L. A. Salako, “Acute psychosis after mefloquine: report of six cases,” Tropical and Geographical Medicine, vol. 47, no. 4, pp. 179–180, 1995. View at: Google Scholar
  18. J. L. Bem, L. Kerr, and D. Stuerchler, “Mefloquine prophylaxis: an overview of spontaneous reports of severe psychiatric reactions and convulsions,” Journal of Tropical Medicine and Hygiene, vol. 95, no. 3, pp. 167–179, 1992. View at: Google Scholar
  19. P. C. Stuiver, R. J. Ligthelm, and T. J. Goud, “Acute psychosis after mefloquine,” The Lancet, vol. 2, no. 8657, p. 282, 1989. View at: Google Scholar
  20. M. M. Van Riemsdijk, J. M. Ditters, M. C. Sturkenboom et al., “Neuropsychiatric events during prophylactic use of mefloquine before travelling,” European Journal of Clinical Pharmacology, vol. 58, no. 6, pp. 441–445, 2002. View at: Publisher Site | Google Scholar
  21. E. Petersen, T. Ronne, A. Ronn, I. Bygbjerg, and S. O. Larsen, “Reported side effects to chloroquine, chloroquine plus proguanil, and mefloquine as chemoprophylaxis against malaria in Danish travelers,” Journal of Travel Medicine, vol. 7, no. 2, pp. 79–84, 2000. View at: Google Scholar
  22. D. N. Durrheim, S. Gammon, S. Waner, and L. E. O. Braack, “Antimalarial prophylaxis—use and adverse events in visitors to the Kruger National Park,” South African Medical Journal, vol. 89, no. 2, pp. 170–175, 1999. View at: Google Scholar
  23. C. Hoebe, J. de Munter, and C. Thijs, “Adverse effects and compliance with mefloquine or proguanil antimalarial chemoprophylaxis,” European Journal of Clinical Pharmacology, vol. 52, no. 4, pp. 269–275, 1997. View at: Publisher Site | Google Scholar
  24. M. M. van Riemsdijk, M. M. van der Klauw, J. A. C. van Heest et al., “Neuro-psychiatric effects of antimalarials,” European Journal of Clinical Pharmacology, vol. 52, no. 1, pp. 1–6, 1997. View at: Publisher Site | Google Scholar
  25. T. Weinke, M. Trautmann, T. Held et al., “Neuropsychiatric side effects after the use of mefloquine,” The American Journal of Tropical Medicine and Hygiene, vol. 45, no. 1, pp. 86–91, 1991. View at: Google Scholar
  26. D. J. Javorsky, G. Tremont, G. I. Keitner, and A. H. Parmentier, “Cognitive and neuropsychiatric side effects of mefloquine,” Journal of Neuropsychiatry and Clinical Neurosciences, vol. 13, no. 2, p. 302, 2001. View at: Publisher Site | Google Scholar
  27. M. M. van Riemsdijk, M. C. Sturkenboom, J. M. Ditters, R. J. Ligthelm, D. Overbosch, and B. H. C. Stricker, “Atovaquone plus chloroguanide versus mefloquine for malaria prophylaxis: a focus on neuropsychiatric adverse events,” Clinical Pharmacology and Therapeutics, vol. 72, no. 3, pp. 294–301, 2002. View at: Publisher Site | Google Scholar
  28. E. Boudreau, B. Schuster, J. Sanchez et al., “Tolerability of prophylactic Lariam regimens,” Tropical Medicine and Parasitology, vol. 44, no. 3, pp. 257–265, 1993. View at: Google Scholar
  29. A. M. Croft and P. Garner, “Mefloquin for preventing malaria in non-immune adult travelers,” Cochrane Database of Systematic Reviews, no. 4, Article ID CD000138, 2000. View at: Google Scholar
  30. Food and Drug Administration, “2002 safety alert: Larium (mefloquine hydrochloride),” 2002, View at: Google Scholar
  31. A. M. Croft and A. Herxheimer, “Adverse effects of the antimalaria drug, mefloquine: due to primary liver damage with secondary thyroid involvement?” BMC Public Health, vol. 2, no. 1, p. 6, 2002. View at: Publisher Site | Google Scholar
  32. R. Speich and A. Haller, “Central anticholinergic syndrome with the antimalarial drug mefloquine,” The New England Journal of Medicine, vol. 331, no. 1, pp. 57–58, 1994. View at: Publisher Site | Google Scholar
  33. R. C. Wittes and R. Saginur, “Adverse reaction to mefloquine associated with ethanol ingestion,” Canadian Medical Association Journal, vol. 152, no. 4, pp. 515–517, 1995. View at: Google Scholar
  34. T. Tanielian and L. H. Jaycox, Eds., Invisible Wounds of War: Psychological and Cognitive Injuries, Their Consequences, and Services to Assist Recovery, RAND Corporation, Santa Monica, Calif, USA, 2008.
  35. R. L. Nevin, “Mefloquine prescriptions in the presence of contraindications: prevalence among US military personnel deployed to Afghanistan, 2007,” Pharmacoepidemiology and Drug Safety, vol. 19, no. 2, pp. 206–210, 2010. View at: Publisher Site | Google Scholar

Copyright © 2011 Alan L. Peterson et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2021, as selected by our Chief Editors. Read the winning articles.