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1

Aronson, J. K. Meyler's side effects of psychiatric drugs. Elsevier, 2009.

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2

Mrazek, David. Psychiatric pharmacogenomics. Oxford University Press, 2010.

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3

Citizens Commission on Civil Rights (U.S.). Psychiatry destroying morals: A travesty of help. Citizens Commission on Human Rights, 1995.

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4

J, Castle David, and Murray, Robin, MD, M Phil, MRCP, MRC Psych, eds. Marijuana and madness: Psychiatry and neurobiology. Cambridge University Press, 2004.

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5

Sabit, Gabay, Harris Joseph, and Ho Beng T. 1932-, eds. Metal ions in neurology and psychiatry. A.R. Liss, 1985.

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6

Breggin, Peter Roger. Medication madness: A psychiatrist exposes the dangers of mood-altering medications. St. Martin's Press, 2008.

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7

Melissa, Piasecki, ed. Nicotine in psychiatry: Psychopathology and emerging therapeutics. American Psychiatric Press, 2000.

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8

Maris, Ronald W. Pillaged: Psychiatric medications and suicide risk. The University of South Carolina Press, 2015.

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9

R, Watson Ronald, and Watzl Bernhard, eds. Nutrition and alcohol. CRC Press, 1992.

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10

J, Peters Timothy, ed. Alcohol misuse: A European perspective. Harwood Academic Publishers, 1996.

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11

American Psychiatric Association. Task Force on Tardive Dyskinesia. Tardive dyskinesia: A task force report of the American Psychiatric Association. The Association, 1992.

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12

Baselt, Randall C. Drug effects on psychomotor performance. Biomedical Publications, 2001.

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13

Paul, Grof, ed. Clinical evaluation of psychotropic drugs for psychiatric disorders: Principles and proposed guidelines. Hogrefe & Huber Publishers, 1993.

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14

E, Polifka Janine, ed. The effects of neurologic and psychiatric drugs on the fetus and nursing infant: A handbook for health care professionals. Johns Hopkins University Press, 1998.

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15

Gerald, Caplan, ed. Helping the helpers not to harm: Iatrogenic damage and community mental health. Brunner-Routledge, 2001.

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16

Pringle, Lidia Wasowicz. Suffer the child: How the American healthcare system is failing our future. Capital Books, 2006.

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17

1795-1831, Bertrand Alexandre-Jacques-François, and Despine Charles-Humbert-Antoine 1777-1852, eds. Hysteria complicated by ecstasy: The case of Nanette Leroux. Princeton University Press, 2010.

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18

Eckart, Rüther, and Hippius Hanns, eds. Tardive dyskinesia. Hogrefe & Huber, 1992.

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19

B, Karch Steven, ed. Forensic issues in alcohol testing. Taylor & Francis, 2007.

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20

Leventhal, Allan M. The myth of depression as disease: Limitations and alternatives to drug treatment. Praeger, 2006.

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21

H, Pollack Mark, Otto Michael W, and Rosenbaum J. F, eds. Challenges in clinical practice: Pharmacologic and psychosocial strategies. Guilford Press, 1996.

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22

1956-, Schneider Jay S., and Gupta Madi, eds. Current concepts in Parkinson's disease research. Hogrefe & Huber, 1993.

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23

Ante, Lundberg, ed. The environment and mental health: A guide for clinicians. Lawrence Erlbaum Associates, 1998.

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24

R, Edelstein Michael. Contaminated communities: The social and psychological impacts of residential toxic exposure. Westview Press, 1988.

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25

A, Glantz Stanton, ed. The cigarette papers. University of California Press, 1996.

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26

Cantwell, Roch. Peripartum psychiatric disorders. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198713333.003.0049.

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Women are at greatest risk of suffering from mental illness during their reproductive years, and at very particular risk in relation to childbirth. Psychological adjustment, social challenges, and neurohormonal changes in pregnancy and parturition may all contribute to this risk. The consequences of maternal mental illness may be severe. Suicide is among the leading causes of maternal death in the United Kingdom and psychiatric factors are implicated in a further significant number of deaths in pregnancy and the first postnatal year. Increasing evidence points to the detrimental effect of untr
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27

Hodgkiss, Andrew. Psychiatric consequences of cancer treatments: hormone and cytokine treatments. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198759911.003.0007.

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The antidepressant and neuroprotective effects of oestradiol are described. Psychiatric consequences of oophorectomy, and treatment with tamoxifen and aromatase inhibitors, are then discussed. Androgen-deprivation therapy has temporary effects on cognitive function and mood that reflect the distribution of androgen receptors in the brain. The rapid-onset adverse psychiatric effects of high-dose glucocorticoids are presented (including ‘steroid psychosis’) and a novel, non-genomic molecular mechanism highlighted. In contrast, the depressive effect of chronic glucocorticoid use is then considere
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28

Medication Madness: True Stories of Mayhem, Murder, and Suicide Caused by Psychiatric Drugs. St. Martin's Press, 2008.

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29

Cavanna, Andrea E. Topiramate. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198791577.003.0013.

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Topiramate is a second-generation antiepileptic drug characterized by a good range of antiepileptic indications, with an acceptable interaction profile in polytherapy. Topiramate has an acceptable behavioural tolerability profile, although it has been associated with a number of negative behavioural effects in patients with epilepsy (in particular depression, irritability, and psychotic symptoms). Identified risk factors for the development of behavioural adverse effects include high starting doses and rapid titration schedules, as well as personal or family history of psychiatric disorders. T
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30

Adverse syndromes and psychiatric drugs: A clinical guide. Oxford University Press, 2004.

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31

Cavanna, Andrea E. Vigabatrin. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198791577.003.0015.

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Vigabatrin is a second-generation antiepileptic drug characterized by a few antiepileptic indications, with a very good interaction profile in polytherapy. Clinically relevant adverse effects (especially visual field defects) have reduced its use as antiepileptic drug in routine clinical practice considerably. Vigabatrin has an acceptable behavioural tolerability profile, although patients with epilepsy treated with this medication can report depression, psychosis, and irritability. Risk factors for developing psychiatric adverse effects include high starting and maintenance doses, past psychi
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32

Keshavan, Matche. Drug-Induced Dysfunction In Psychiatry. Taylor & Francis, 1991.

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33

Cavanna, Andrea E. Zonisamide. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198791577.003.0016.

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Zonisamide is a second-generation antiepileptic drug characterized by a few antiepileptic indications, with an acceptable interaction profile in polytherapy. Zonisamide has an acceptable tolerability profile in patients with epilepsy, with depression, irritability, agitation and psychosis as the most commonly reported psychiatric adverse effects. Zonisamide has no approved indications or clinical uses in psychiatry, as initial findings from uncontrolled studies suggesting effectiveness in the treatment of patients with bipolar disorder did not find confirmation. There is preliminary evidence f
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34

Balon. Practical Management of the Side Effects of Psychotropic Drug (Medical Psychiatry , Vol 12). Informa Healthcare, 1999.

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35

Campbell, Magda, Paul Grof, and M. Iftikhar Akhter. Clinical Evaluation of Psychotropic Drugs for Psychiatric Disorders: Principles and Proposed Guidelines (Who Expert Series on Biological Psychiatry,). Hogrefe & Huber Pub, 1993.

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36

Brown, James S. Environmental and Chemical Toxins and Psychiatric Illness. American Psychiatric Association Publishing, 2008.

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37

Brown, James S. Environmental and Chemical Toxins and Psychiatric Illness. American Psychiatric Publishing, Inc., 2002.

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38

Watson, Ronald R., and Bernhard Watzl. Nutrition and Alcoholthe CRC Series in Physiology of Drug Abuse. CRC, 1992.

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39

Ect: Basic Mechanisms. Amer Psychiatric Pub, 1986.

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40

Toxic psychiatry. St. Martin's Press, 1994.

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41

Remembering Ritalin: A doctor and generation Rx reflect on life and psychiatric drugs. Penguin Group, 2011.

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42

Remembering Ritalin: A doctor and generation Rx reflect on life and psychiatric drugs. Penguin, 2012.

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43

Peters. Alcohol Misuse; A European Perspective. CRC, 1996.

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44

Tranquil prisons: Chemical incarceration under community treatment orders. University of Toronto Press, 2011.

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45

Tardive dyskinesia: A task force report of the American Psychiatric Association. American Psychiatric Association, 1992.

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46

Drug Effects on Psychomotor Performance. CHEMICAL TOXICOLOGY, 2000.

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47

Hodgkiss, Andrew. Opportunities for prevention, or early detection, of psychopathology. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198759911.003.0010.

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The value of informing patients and carers about the possible psychiatric consequences of specific cancers and cancer treatments is emphasized. Eight examples follow, of cancer treatments where formal consent concerning possible adverse psychiatric effects is indicated. Modest modifications of certain oncological treatments can reduce the incidence of psychopathology—seven examples are offered. Proactive monitoring of endocrine status, serum electrolytes, or vitamin B12 levels during or after particular treatments is advocated to prevent psychopathology. The chapter closes with practical recom
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48

Cavanna, Andrea E. Lamotrigine. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198791577.003.0007.

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Lamotrigine is a second-generation antiepileptic drug characterized by a wide range of antiepileptic indications, with an acceptable interaction profile in polytherapy. It has a good behavioural tolerability profile and a wide range of psychiatric uses. In patients with epilepsy, lamotrigine has shown antidepressant properties, as well as mixed effects on anxiety symptoms. Adverse behavioural effects (irritability, agitation, and aggression) are not very common and are usually observed in patients with learning disability. Lamotrigine has a licensed indication for the prevention of depressive
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49

Post, Robert M. Depression as a Recurrent, Progressive Illness. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190603342.003.0003.

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Clinical Highlights and summary of Chapter• Episodes of depression and bipolar illness progress in two ways:faster recurrences as a function of number of prior episodes, andgreater autonomy (decreased need for precipitation by stressors(Episode Sensitization)• Recurrent stressors result in increased reactivity to subsequent stressors(Stress sensitization) and bouts of stimulant abuse increase in severity with repetition(Stimulant-induced behavioral sensitization)• Each type of sensitization cross-sensitizes to the others and drives illness progression• Each type of sensitization involves speci
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50

Gorman, Jack M. Introduction. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190850128.003.0001.

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After World War II, mental health turned toward psychopharmacology, the use of medications to treat psychiatric illnesses, as its mainstay. The success of medications led some to insist that all mental illness is due to the inheritance of abnormal genes and that life’s experiences play a diminished role. This alienated many who believe that psychotherapy is also an effective way of treating these disorders and led to a mistrust of neuroscience research. Some insisted that neuroscience ignores the human “mind.” In fact, neuroscience research in the past 50 years has clearly shown that adverse l
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