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Kubanek, A. Sertraline in Hemodialysis Patients. Encyclopedia. Available online: (accessed on 02 March 2024).
Kubanek A. Sertraline in Hemodialysis Patients. Encyclopedia. Available at: Accessed March 02, 2024.
Kubanek, Alicja. "Sertraline in Hemodialysis Patients" Encyclopedia, (accessed March 02, 2024).
Kubanek, A. (2021, September 22). Sertraline in Hemodialysis Patients. In Encyclopedia.
Kubanek, Alicja. "Sertraline in Hemodialysis Patients." Encyclopedia. Web. 22 September, 2021.
Sertraline in Hemodialysis Patients

Depression and anxiety are the most common psychiatric disorders in end-stage renal disease (ESRD) patients treated with hemodialysis (HD) and may correlate with lower quality of life and increased mortality. Depression treatment in HD patients is still a challenge both for nephrologists and psychiatrists. The possible treatment of depressive disorders can be pharmacological and non-pharmacological. In our article, we focus on the use of sertraline, the medication which seems to be relatively safe and efficient in the abovementioned population, taking under consideration several limitations regarding the use of other selective serotonin reuptake inhibitors (SSRIs).

depression hemodialysis sertraline

1. Introduction

Depression and anxiety are the most common psychiatric disorders in end-stage renal disease (ESRD) patients treated with hemodialysis (HD). Their prevalence is increasing in recent years [1], reaching the rate of 20–40% for depression [2][3] and 20–52% for anxiety [4], depending on the methodological approach. According to the studies, these psychiatric disorders may correlate with lower quality of life, increased hospitalization rate, suicidal behavior, hemodialysis nonadherence, and increased mortality [5]. Despite the number of studies on this issue, major depressive disorder (MDD) in ESRD patients is still underdiagnosed, and its treatment is not optimal [6] [Table 1]. Anxiety disorders seem to be overlooked even more often [7], which is probably associated with significant overlapping of symptoms with depression [8]. As initiation of dialysis is a large change in everyday functioning with a potential to induce or worsen psychiatric symptoms, screening for depression [9] and anxiety is suggested at the beginning of renal replacement treatment.

Table 1. Comparison of depression in ICD-10 and DSM-5 classifications.
Subject of Comparison ICD-10 Classification DSM-5 Classification
Nomenclature Depressive Episode [10] Major depressive disorder (MDD) [11]
Main symptoms
  • Depressed mood to the degree that is definitely abnormal for the individual, present for most of the day and almost every day, largely uninfluenced by circumstances
  • Loss of interest or pleasure in activities that are normally pleasurable
  • Decreased energy or increased fatiguability [10]
  • Depressed mood most of the day, nearly every day, as indicated in the subjective report or in observation made by others
  • Markedly diminished interest in pleasure in all or almost all activities most of the day and nearly every day
Additional symptoms
  • Loss of confidence and self-esteem
  • Unreasonable feelings of self-reproach or excessive and inappropriate guilt
  • Recurrent thoughts of death or suicide, or any suicidal behaviour
  • Complaints or evidence of diminished ability to think or concentrate, such as indecisiveness or vacillation
  • Change in psychomotor activity with agitation or retardation (either subjective or objective)
  • Sleep disturbance of any type
  • Change in appetite (decrease or increase) with corresponding weight change) [10]
  • Significant weight loss when not dieting or weight gain, for example, more than 5 percent of body weight in a month or changes in appetite nearly every day
  • Insomnia or hypersomnia nearly every day
  • Psychomotor agitation or retardation nearly every day
  • Fatigue or loss of energy nearly every day
  • Feelings of worthlessness or excessive or inappropriate guilt
  • Diminished ability to think or concentrate, or indecisiveness nearly every day
  • Recurrent thoughts of death [11]
Diagnostic criteria At least two main symptoms and additional symptoms in a total number of at least four [10] At least one main symptom and additional symptoms in a total number of at least
Duration of symptoms At least two weeks [10] At least two weeks [11]
Severity of symptoms Clinical differentiation:
  • Mild Depressive Episode (at least two main symptoms and additional symptoms with a total number of at least four)
  • Moderate Depressive Episode (at least two main symptoms and additional symptoms with a total number of at least six)
  • Severe Depressive Episode (all three main symptoms and additional symptoms with a total number of at least eight) [10]
The symptoms ought to cause significant impairment in social, occupational or another important area of functioning [11]
Exclusion criteria
  • No hypomanic or manic symptoms sufficient to meet the criteria for hypomanic or manic episode at any time in the individual’s life
  • The episode is not attributable to psychoactive substance use
  • The episode is not attributable to any organic mental disorder [10]
  • No preceding manic or hypomanic episode
  • The disorder is not connected with psychological effects of the substance use or another medical condition
  • The disorder cannot be better explained by schizophrenia or any other psychotic disorder [11]
The possible treatment of depressive and anxiety disorders can be pharmacological and non-pharmacological. The first choice drugs for both of the above are selective serotonin reuptake inhibitors (SSRIs), including citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, and sertraline Table 2 [12][13]. While their administration is widely considered to be safe and effective in ESRD patients, further studies are still needed in this field [14]. Non-pharmacological interventions may include psychotherapy, mindfulness meditation, and frequent HD [15].
Table 2. Antidepressive agents with serotonin reuptake transporter (SERT) inhibition activity.
Citalopram Desvenlafaxine Nefazodone Amoxapine Vilazodone Amitriptyline
Escitalopram Duloxetine Trazodone   Vortioxetine Clomipramine
Fluoxetine Levomilnacipram       Desipramine
Fluvoxamine Milnacipran       Doxepin
Paroxetine Venlafaxine       Imipramine
Sertraline         Nortriptyline
In our article, we focus on the use of sertraline due to several limitations regarding the use of other SSRIs in ESRD patients. Fluoxetine and fluvoxamine are considered to be less efficacious [16]. Moreover, fluvoxamine has a significant impact on liver metabolism of other drugs. Administering citalopram and escitalopram bears the risk of increasing QTc interval in doses larger than 20 mg and 10 mg, respectively. These doses have been set as maximum for elderly patients [17][18], limiting therapeutical options with these drugs in many ESRD patients. While there have recently been voices raising doubts about decisions limiting the use of citalopram and escitalopram [19], these restrictions still stand. In view of the above, sertraline may seem like a relatively safe and efficient medication. However, before administering, one should consider several side effects particularly significant in the treatment of ESRD patients. These adverse effects, along with specific benefits, are discussed below in Table 3 and and Figure 1.
Figure 1. Possible effects of sertraline in the hemodialysis patient.
Table 3. Effects of sertraline use in hemodialysis patients.
Impact on QTc Prolongation Safe While Provided in Recommended Doses [20]
Bleeding Increases the risk of bleeding [21][22]
Platelet reactivity May reduce platelet activation [23][24][25]
Intradialytic hypotension (IDH) Inconsistent study results, may reduce the risk of IDH [26][27][28][29][30]
Chronic kidney disease-associated pruritus (CKD-aP) Can reduce pruritus in cases caused by CKD [31][32][33]
Cytokines Reduces the concentration of pro-inflammatory and increases the levels of anti-inflammatory cytokines, insufficient data in HD population [34][35][36]
Sexual disfunction (SD) Negative impact on SD in general population [37][38] and in HD population [39]
Fracture risk and osteoporosis Is associated with hip fracture risk and may decrease bone mass in general population [40][41], may increase fracture risk in ESRD population [42]

2. Sertraline—General Properties of the Medication

Studies evaluating sertraline’s safety and efficacy in ESRD patients performed so far usually had small samples and lacked placebo control [39]; therefore, in further parts of this article, references are also made to data from the general population. The European Renal Best Practice (ERBP) guidelines suggest that trials with SSRIs in patients who meet criteria for moderate Major Depressive Disorder (MDD) should last for 8–12 weeks, after which the effect of the treatment should be evaluated [43]. This is rather inconsistent with the psychiatric clinical practice when the first evaluation for depressive and anxiety patients is usually done after 4 weeks with considerations of temporizing, increasing the dose, switching to another antidepressant, or combining several drugs in patients with minimal response or safety issues [44][45].
Before starting the treatment with sertraline, no specific medical tests are required [46]. To minimize side effects, psychiatrists usually start with a subtherapeutic dose of 25 mg for one week with an increase to 50 mg after this period. These means of precaution should be especially considered in patients with coexisting anxiety, in advanced age, and those more susceptible to side effects. While doses up to 300 mg have been used, the maximum dose is considered to be 200 mg. ERBP guidelines do not suggest any need to change the dosing in stages 3–5 of chronic kidney disease (CKD), but some studies suggest that smaller doses of sertraline may be required in ESRD patients, yet the post-hemodialysis supplementation is suggested to be unnecessary [47]. The effect of the treatment can be usually seen after 4–6 weeks. The drug should be taken daily. While most psychiatrists and patients prefer it to be taken in the morning, some patients may experience sedation, and an evening dosage would be more appropriate. The general rule is that sertraline should be taken every day in the same regimen (time of day, dose splitting, with or without food). Due to a fairly long half-life time (66 h in the general population when including its less active metabolite, norsetraline) [48], missing a single dose should not result in any withdrawal side effects. This is also the reason why this drug is relatively easy to discontinue. Sertraline is a moderate inhibitor of CYP2B6 and CYP2D6 with a dose-dependent effect of increasing other drugs metabolized through these pathways [49]. Effect on other CYP450 subunits is not clinically significant, and its interactions are less potent than these of fluoxetine, fluvoxamine, or paroxetine.
Sertraline is considered to be safe to use. The adverse effects that seem to be more common while using sertraline compared to other SSRIs are diarrhea and activation [50]. In some cases, drowsiness, headache, or sexual dysfunctions may appear [50]. One should also keep in mind the antiplatelet effect of sertraline, which, while in some cases beneficial [51], may be an issue in patients with greater bleeding risk [52]. Modification of antidepressant treatment needs to be considered in some patients [53]. Regularly observed practice is also an adjustment of antiplatelet therapy dose (for instance, by reducing acetylsalicylic acid dose from 150 mg to 75 mg) after adding sertraline. This course of action, however, has no support in current literature.
Adverse effects during sertraline administration are usually mild and can be alleviated by changing the treatment regimen (lowering the dose, changing the time of administration, splitting the dose into BID (two times a day) or TID (three times a day), adding low doses of trazodone for sexual dysfunctions or insomnia, etc.) [54][55].
The general rule during antidepressant treatment is that we should struggle to achieve full remission and continue administration of the drug for the maintenance period of at least 6 months before any attempts of down-titrating or discontinuing the medication [56].


  1. Saran, R.; Robinson, B.; Abbott, K.C.; Bragg-Gresham, J.; Chen, X.; Gipson, D.; Gu, H.; Hirth, R.A.; Hutton, D.; Jin, Y.; et al. US Renal Data System 2019 Annual Data Report: Epidemiology of Kidney Disease in the United States. Am. J. Kidney Dis. 2020, 75 (Suppl. S1), A6–A7.
  2. Palmer, S.; Vecchio, M.; Craig, J.C.; Tonelli, M.; Johnson, D.W.; Nicolucci, A.; Pellegrini, F.; Saglimbene, V.; Logroscino, G.; Fishbane, S.; et al. Prevalence of depression in chronic kidney disease: Systematic review and meta-analysis of observational studies. Kidney Int. 2013, 84, 179.
  3. King-Wing Ma, T.; Kam-Tao Li, P. Depression in dialysis patients. Nephrology 2016, 21, 639–646.
  4. Murtagh, F.E.; Addington-Hall, J.; Higginson, I.J. The prevalence of symptoms in end-stage renal disease: A systematic review. Adv. Chronic Kidney Dis. 2007, 14, 82–99.
  5. Bautovich, A.; Katz, I.; Smith, M.; Loo, C.K.; Harvey, S.B. Depression and chronic kidney disease: A review for clinicians. Aust. N. Z. J. Psychiatry 2014, 48, 530–541.
  6. Hedayati, S.S.; Yalamanchili, V.; Finkelstein, F.O. A practical approach to the treatment of depression in patients with chronic kidney disease and end-stage renal disease. Kidney Int. 2012, 81, 247–255.
  7. Schouten, R.W.; Haverkamp, G.L.; Loosman, W.L.; Chandie Shaw, P.K.; van Ittersum, F.J.; Smets, Y.F.C.; Vleming, L.J.; Dekker, F.W.; Honig, A.; Siegert, C.E.H. Anxiety symptoms, mortality and hospitalization in patients receiving maintenance dialysis: A cohort study. Am. J. Kidney Dis. 2019, 74, 158–166.
  8. Cohen, S.D.; Cukor, D.; Kimmel, P.L. Anxiety in Patients Treated with Hemodialysis. Clin. J. Am. Soc. Nephrol. 2016, 11, 2250–2255.
  9. Cohen, S.D.; Norris, L.; Aquaviva, K.; Peterson, R.A.; Kimmel, P.L. Screening, diagnosis and treatment of depression in patients with end-stage renal disease. Clin. J. Am. Soc. Nephrol. 2007, 2, 133–142.
  10. World Health Organization. The ICD-10 Classification of Mental and Behavioural Disorders: Diagnostic Criteria for Research; World Health Organization: Geneva, Switzerland, 1993; p. 248.
  11. American Psychiatric Association. DSM-5 Task Force. Diagnostic and Statistical Manual of Mental Disorders: DSM-5; American Psychiatric Association: Arlington, VA, USA, 2013. Available online: (accessed on 1 September 2021).
  12. Fasipe, O.J. Neuropharmacological classification of antidepressant agents based on their mechanisms of action. Arch. Med. Health Sci. 2018, 6, 81–94.
  13. Hughes, Z.A.; Starr, K.R.; Langmead, C.J.; Hill, M.; Bartoszyk, G.D.; Hagan, J.J.; Middlemiss, D.N.; Dawson, L.A. Neurochemical evaluation of the novel 5-HT1A receptor partial agonist/serotonin reuptake inhibitor, vilazodone. Eur. J. Pharmacol. 2005, 510, 49–57.
  14. Constantino, J.L.; Fonseca, V.A. Pharmacokinetics of antidepressants in patients undergoing hemodialysis: A narrative literature review. Braz. J. Psychiatry 2019, 41, 441–446.
  15. Jaber, B.L.; Lee, Y.; Collins, A.J.; Hull, A.R.; Kraus, M.A.; McCarthy, J.; Miller, B.W.; Spry, L.; Finkelstein, F.O. Effect of daily hemodialysis on depressive symptoms and postdialysis recovery time: Interim report from the FREEDOM (Following Rehabilitation, Economics and Everyday-Dialysis Outcome Measurements) Study. Am J Kidney Dis. 2010, 56, 531–539.
  16. Cipriani, A.; Furukawa, T.A.; Salanti, G.; Chaimani, A.; Atkinson, L.Z.; Ogawa, Y.; Leucht, S.; Ruhe, H.G.; Turner, E.H.; Higgins, J.P.T.; et al. Comparative efficacy and acceptability of 21 antidepressant drugs for the acute treatment of adults with major depressive disorder: A systematic review and network meta-analysis. Lancet 2018, 391, 1357–1366.
  17. US Food and Drug Administration. FDA Drug Safety Communication: Revised Recommendations for Celexa (Citalopram Hydrobromide) Related to a Potential Risk of Abnormal Heart Rhythms with High Doses. US Food and Drug Administration (2012). Available online: (accessed on 1 September 2021).
  18. Health Canada 2012 Health CanadaAntidepressant cipralex (Escitalopram): Updated information Regarding Dose-Related Heart Risk. 2012. Available online: (accessed on 3 January 2021).
  19. Crépeau-Gendron, G.; Brown, H.K.; Shorey, C.; Madan, R.; Szabuniewicz, C.; Koh, S.; Veinish, S.; Mah, L. Association between citalopram, escitalopram and QTc prolongation in a real-world geriatric setting. J. Affect. Disord. 2019, 250, 341–345.
  20. Assimon, M.M.; Brookhart, M.A.; Flythe, J.E. Comparative Cardiac Safety of Selective Serotonin Reuptake Inhibitors among Individuals receiving Maintenance Hemodialysis. J. Am. Soc. Nephol. 2019, 30, 611–623.
  21. Jiang, H.Y.; Chen, H.Z.; Hu, X.J.; Yu, Z.H.; Yang, W.; Deng, M.; Zhang, Y.H.; Ruan, B. Use of selective serotonin reuptake inhibitors and risk of upper gastrointestinal bleeding: A systematic review and meta-analysis. Clin. Gastroenterol. Hepatol. 2015, 13, 42–50.
  22. Iwagami, M.; Tomlinson, L.A.; Mansfield, K.E.; Douglas, I.J.; Smeeth, L.; Nitsch, D. Gastrointestinal bleeding risk of selective serotonin reuptake inhibitors by level of kidney function: A population-based cohort study. Br. J. Clin. Pharmacol. 2018, 84, 2142–2151.
  23. Lopez-Vilchez, I.; Serra-Millas, M.; Navarro, V.; Rosa Hernandez, M.; Villalta, J.; Diaz-Ricart, M.; Gasto, C.; Escolar, G.; Galan, A.M. Prothrombotic platelet phenotype in major depression: Downregulation by antidepressant treatment. J. Affect. Disord. 2014, 159, 39–45.
  24. Tseng, Y.L.; Chiang, M.L.; Lane, H.Y.; Su, K.P.; Lai, Y.C. Selective serotonin reuptake inhibitors reduce P2Y12 receptor-mediated amplification of platelet aggregation. Thromb. Res. 2013, 131, 325–332.
  25. Acedillo, R.R.; Shah, M.; Devereaux, P.J.; Li, L.; Iansavichus, A.V.; Walsh, M.; Garg, A.X. The risk of perioperative bleeding in patients with chronic kidney disease: A systematic review and meta-analysis. Ann. Surg. 2013, 258, 901–913.
  26. Molin, C.Z.Z.D.; Sakae, T.M.; Schuelter-Trevisol, F.; Trevisol, D.J. Effects of sertraline in the prevention of low blood pressure in patients undergoing hemodialysis. J. Bras. Nefrol. 2019, 41, 492–500.
  27. Razeghi, E.; Dashti-Khavidaki, S.; Nassiri, S.; Abolghassemi, R.; Khalili, H.; Nazari, S.S.H.; Mansournia, A.M.; Taraz3, M. A randomized crossover clinical trial of sertraline for intradialytic hypotension. Iran. J. Kidney Dis. 2015, 9, 323–330.
  28. Yalcin, A.U.; Sahin, G.; Erol, M.; Bal, C. Sertraline hydrochloride treatment for patients with hemodialysis hypotension. Blood Purif. 2002, 20, 150–153.
  29. Yalcin, A.U.; Kudaiberdieva, G.; Sahin, G.; Gorenek, B.; Akcar, N.; Kuskus, S.; Bayrak, F.; Timuralp, B. Effect of sertraline hydrochloride on cardiac autonomic dysfunction in patients with hemodialysis-induced hypotension. Nephron Physiol. 2003, 93, 21–28.
  30. Brewster, U.C.; Ciampi, M.A.; Abu-Alfa, A.K.; Perazella, M.A. Addition of sertraline to other therapies to reduce dialysis-associated hypotension. Nephrology 2003, 8, 296–301.
  31. Shakiba, M.; Sanadgol, H.; Azmoude, H.R.; Mashhadi, M.A.; Sharifi, H. Effect of sertraline on uremic pruritus improvement in ESRD patients. Int. J. Nephrol. 2012, 2012, 363901.
  32. Chan, K.Y.; Li, C.W.; Wong, H.; Yip, T.; Chan, M.L.; Cheng, H.W.; Sham, M.K. Use of sertraline for antihistamine-refractory uremic pruritus in renal palliative care patients. J. Palliat. Med. 2013, 16, 966–970.
  33. Pakfetrat, M.; Malekmakan, L.; Hashemi, N.; Tadayon, T. Sertraline can reduce uremic pruritus in hemodialysis patient: A double blind randomized clinical trial from Southern Iran. Hemodial. Int. 2018, 22, 103–109.
  34. Al-Hakeim, H.K.; Twayej, A.J.; Al-Dujaili, A.H. Reduction in serum IL-1β IL-6, and IL-18 levels and Beck Depression Inventory-II score by combined sertraline and ketoprofen administration in major depressive disorder: A clinical trial. Neurol. Psychiatry Brain Res. 2018, 30, 148–153.
  35. Sutcigil, L.; Oktenli, C.; Musabak, U.; Bozkurt, A.; Cansever, A.; Uzun, O.; Sanisoglu, S.Y.; Yesilova, Z.; Ozmenler, N.; Ozsahin, A.; et al. Pro- and anti-inflammatory cytokine balance in major depression: Effect of sertraline therapy. Clin. Dev. Immunol. 2007, 2007, 1–6.
  36. Taraz, M.; Khatami, M.R.; Dashti-Khavidaki, S.; Akhonzadeh, S.; Noorbala, A.A.; Ghaeli, P.; Taraz, S. Sertraline decreases serum level of interleukin-6 (IL-6) in hemodialysis patients with depression: Results of a randomized double-blind, placebo-controlled clinical trial. Int. Immunopharmacol. 2013, 17, 917–923.
  37. Khazaie, H.; Rezaie, L.; Rezaei Payam, N.; Najafi, F. Antidepressant-induced sexual dysfunction during treatment with fluoxetine, sertraline and trazodone; a randomized controlled trial. Gen. Hosp. Psychiatry 2015, 37, 40–45.
  38. Serretti, A.; Chiesa, A. Treatment-emergent sexual dysfunction related to antidepressants: A meta-analysis. J. Clin. Psychopharmacol. 2009, 29, 259–266.
  39. Palmer, S.C.; Natale, P.; Ruospo, M.; Saglimbene, V.M.; Rabindranath, K.S.; Craig, J.C.; Strippoli, G.F. Antidepressants for treating depression in adults with end-stage kidney disease treated with dialysis. Cochrane Database Syst. Rev. 2016, 5, CD004541.
  40. Khanassov, V.; Hu, J.; Reeves, D.; van Marwijk, H. Selective serotonin reuptake inhibitor and selective serotonin and norepinephrine reuptake inhibitor use and risk of fractures in adults: A systematic review and meta-analysis. Int. J. Geriatr. Psychiatry 2018, 33, 1688–1708.
  41. Rabenda, V.; Nicolet, D.; Beaudart, C.; Bruyère, O.; Reginster, J.-Y. Relationship between use of antidepressants and risk of fractures: A meta-analysis. Osteoporos. Int. 2013, 24, 121–137.
  42. Vangala, C.; Niu, J.; Montez-Rath, M.E.; Yan, J.; Navaneethan, S.D.; Winkelmayer, W.C. Selective Serotonin Reuptake Inhibitor Use and Hip Fracture Risk Among Patients on Hemodialysis. Am. J. Kidney Dis. 2020, 75, 351–360.
  43. Nagler, E.V.; Webster, A.C.; Vanholder, R.; Zoccali, C. Antidepressants for depression in stage 3–5 chronic kidney disease: A systematic review of pharmacokinetics, efficacy and safety with recommendations by European Renal Best Practice (ERBP). Nephrol. Dial. Transplant. 2012, 27, 3736–3745.
  44. Hirschfeld, R.M.; Montgomery, S.A.; Aguglia, E.; Amore, M.; Delgado, P.L.; Gastpar, M.; Hawley, C.; Kasper, S.; Linden, M.; Massana, J.; et al. Partial response and nonresponse to antidepressant therapy: Current approaches and treatment options. J. Clin. Psychiatry. 2002, 63, 826–837.
  45. Fredman, S.J.; Fava, M.; Kienke, A.S.; White, C.N.; Nierenberg, A.A.; Rosenbaum, J.F. Partial response, nonresponse, and relapse with selective serotonin reuptake inhibitors in major depression: A survey of current “next-step” practices. J. Clin. Psychiatry 2000, 61, 403–408.
  46. Labbate, L.A.; Fva, M.; Rosenbaum, J.F.; Avana, G.W. Drugs for the treatment of depression. In Handbook of Psychiatric Drug Therapy, 6th ed.; Lippincott Williams & Wilkins: Philadelphia, PA, USA, 2010; p. 54.
  47. Schwenk, M.H.; Verga, M.A.; Wagner, J.D. Hemodialyzability of sertraline. Clin. Nephrol. 1995, 44, 121–124.
  48. Brunton, L.; Chabner, B.; Knollman, B. Goodman and Gilman’s The Pharmacological Basis of Therapeutics, 12th ed.; McGraw Hill Professional: New York, NY, USA, 2010; ISBN 9780071769396.
  49. DeVane, C.L.; Liston, H.L.; Markowitz, J.S. Clinical pharmacokinetics of sertraline. Clin. Pharmacokinet. 2002, 41, 1247–1266.
  50. Hu, X.H.; Bull, S.A.; Hunkeler, E.M.; Ming, E.; Lee, J.Y.; Fireman, B.; Markson, L.E. Incidence and duration of side effects and those rated as bothersome with selective serotonin reuptake inhibitor treatment for depression: Patient report versus physician estimate. J. Clin. Psychiatry 2004, 65, 959.
  51. Serebruany, V.L.; Glassman, A.H.; Malinin, A.I.; Nemeroff, C.B.; Musselman, D.L.; van Zyl, L.T.; Finkel, M.S.; Krishnan, K.R.; Gaffney, M.; Harrison, W.; et al. Sertraline AntiDepressant Heart Attack Randomized Trial Study Group. Platelet/endothelial biomarkers in depressed patients treated with the selective serotonin reuptake inhibitor sertraline after acute coronary events: The Sertraline AntiDepressant Heart Attack Randomized Trial (SADHART) Platelet Substudy. Circulation 2003, 108, 939–944.
  52. Labos, C.; Dasgupta, K.; Nedjar, H.; Turecki, G.; Rahme, E. Risk of bleeding associated with combined use of selective serotonin reuptake inhibitors and antiplatelet therapy following acute myocardial infarction. CMAJ 2011, 183, 1835–1843.
  53. Halperin, D.; Reber, G. Influence of antidepressants on hemostasis. Dialogues Clin. Neurosci. 2007, 9, 47–59.
  54. Sienaert, P. Managing the Adverse Effects of Antidepressants. Psychiatr. Times 2014, 31. Available online: (accessed on 25 January 2021).
  55. Stryjer, R.; Spivak, B.; Strous, R.D.; Shiloh, R.; Harary, E.; Polak, L.; Birgen, M.; Kotler, M.; Weizman, A. Trazodone for the treatment of sexual dysfunction induced by serotonin reuptake inhibitors: A preliminary open-label study. Clin. Neuropharmacol. 2009, 32, 82–84.
  56. Keller, M.B. The long-term treatment of depression. J. Clin. Psychiatry 1999, 60 (Suppl. S17), 41–45.
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