Skip to main content
Materia Socio-Medica logoLink to Materia Socio-Medica
. 2020 Jun;32(2):131–134. doi: 10.5455/msm.2020.32.131-134

Assessment of the Antidepressant Side Effects Occurrence in Patients Treated in Primary Care

Enisa Ramic 1, Subhija Prasko 2, Larisa Gavran 2, Emina Spahic 3
PMCID: PMC7428926  PMID: 32843862

Abstract

Introduction:

It is an undeniable fact that antidepressants can cause side effects. Antidepressants generally have a similar effect but they differ in their application safety, as well as their side effects.

Aim:

To determine differences in the frequency and intensity of antidepressant induced side effects in patients treated in primary care.

Methods:

The research was designed as a prospective, cross-sectional study, conducted on a voluntary and anonymous basis, and it included depression patients treated with antidepressant medications during 2013-2015 in Zenica-Doboj Canton using the Hamilton Depression Rating Scale and Toronto Side Effects Scale.

Results:

The total sample included 508 subjects. As a significant problem, abdominal pain was felt by 14% of subjects, indigestion by 19% of subjects, nausea by 15% of subjects, diarrhea by 9% of subjects, and constipation by 11% of subjects. 29% of subjects suffered from sweating, 20% suffered from a sudden heat stroke, 10% suffered from swelling, and 23% of them reported suffering from dry mouth as a significant problem. The prevalence of side effects in relation to how do they affect life and daily activities of subjects is statistically significant (P <0.000). Statistically significant side effects of SSRI antidepressants correlate with the duration of our subject’s treatment: perception of increased sleep (0.039) as well as decreased sleep (P = 0.009), sweating (P <0.001), sudden heat stroke (P <0.001), being without orgasm (P = 0.004), decreased libido (P <0.001), weight loss (P = 0.045).

Conclusion:

It is necessary to educate the patients about the nature and features of the depressive disorder, and to notify the patients of the expected course of recovery, as well as the need to adhere to the recommended therapy and the possible side effects of the medication.

Keywords: depression, antidepressants, side effects of antidepressants

1. INTRODUCTION

Depression is a disease of our modern age and it presents a great challenge not only for mental health professionals, but also for family medicine physicians (1). It is estimated that over 120 millions of people from all over the world suffer from depression, of which twice as many are women. Depression is expected to become the world’s second significant health problem by 2020. Most of the patients who suffer from depression are between 35 and 55 years old (2).

The first step in the treatment of depression is to set a boundary between the domain of family medicine physicians and the domain of psychiatrists (3). According to the experiences of various authors, mild and moderate depression are in the domain of family medicine physicians. Their responsibility is not only the first contact with a patient, but also the monitoring of the patient treated by a psychiatrist.

Antidepressants generally have a similar effect, but they differ in their safety and side effects. A large number of antidepressants side effects is related to their effect on various neurotransmitter systems (4). The adverse reactions of antidepressants and the irrational use of these medicaments may be related to the low level of research in this domain and the lack of awareness among physicians about this problem (5).

In some patients antidepressants have an effective therapeutic effect, in some patients they cause a development of only mild, almost imperceptible side effects, while in some patients who suffer from mild depressive disorders they can cause a development of a severe chronic depression (6, 7). Individual hypersensitivity to the drug; age; sex; type of antidepressant based on its pharmacological effect; duration of the therapy; polypragmasia; and other things are also important in the assessment of antidepressant side effects (2).

The main reason for discontinuing the treatment with antidepressants is a development of unwanted side effects. It is an undeniable fact that antidepressants can cause side effects (6). Depression and anxiety are very common symptoms that occur when discontinuing the treatment with antidepressants. In this case of adverse drug reactions the clinical manifestation is more severe. Unfortunately, these symptoms are usually misjudged as a recurrent episode of depression, so a patient continues to take an antidepressant, thereby creating a vicious circle. The group of antidepressants called Selective Serotonin Reuptake Inhibitors (SSRIS) are the most frequently prescribed ones nowadays. Known side effects of treatment with SSRIs that are common are: anxiety, restlessness, insomnia, dry mouth, overweight, nausea, diarrhea, sweating, headaches, dizziness, decreased libido, tremor and sexual difficulties (8, 9, 10).

The most commonly noticed side effects of Venlafaxine are: nausea, insomnia, dry mouth, sleepiness, dizziness, constipation, sweating, anxiety, asthenia, sexual difficulties (ejaculation disorder), hypertension and palpitations (9, 10). Tricyclic antidepressants tend to cause more side effects than other antidepressants because of their broad mechanism of action. Drowsiness is a very common side effect, especially in the first few weeks after starting with the treatment. These antidepressants may cause cardiac arrhythmias, obesity, loss of libido, dizziness and nausea, dry mouth, blurred vision, constipation, impaired mycitis, and impaired mystic function with confusion (6, 8). Monoamine oxidase inhibitors (IMAOs) are the oldest group of antidepressants. Common side effects of these medications are dizziness, insomnia, weight gain, headaches, sexual problems, and daytime sleepiness (7, 11).

2. AIM

To determine differences in the frequency and intensity of antidepressant induced side effects in patients treated in primary care. Including factors were diagnosis of depressive dissorder without phsyhotic simptoms or other comorbidities and treatment with antidepressive drugs in duration of minimaly three months.

3. PATIENTS AND METHODS

The research was designed as a prospective, cross-sectional study, conducted on a voluntary and anonymous basis, and it included depression patients treated with antidepressant medications during 2013-2015 in Zenica-Doboj Canton using the Hamilton Depression Rating Scale and Toronto Side Effects Scale.

Questionnaires

Objective screening tests were used in the research: Hamilton Depression Rating Scale (12). The Toronto Side Effects Scale (TSES) which contains 32 items was also used in this research (13). It has been created for a direct evaluation of antidepressants side effects on the central nervous system, gastrointestinal tract and it also relates to sexual difficulties, their frequency and intensity (14, 15). Answers were based on intensity and severity of symptoms.

Statistical Data Analysis

The analysis of results was performed by using the standard Statistical Package for the Social Sciences (SPSS) version 19.0. Standard methods of descriptive statistics were applied in the statistical analysis of results. The χ2-test and the t-test (p <0.05) were used in order to test the statistical significance of the difference of the selected variables. A non-parametric Spearman’s rank correlation test and multivariate regression analysis of variance ANOVA were helpful in multivariate correlation analyzes.

4. RESULTS

A total sample included n = 508 subjects. The average age of the subjects (n = 508) was 48.98 years ± 11.585 years (standard deviation, SD). The highest number of subjects treating an episode of depression were women, 320 out of 508 (63%), and between 41 and 60 years of age (59%). Only 10% patients achieved remission and absence of the depressive disorder as a successful treatment outcome. 20% patients suffered from mild depressive disorder, and 21% patients from moderately severe depression. Serious depression was recorded in 17%, and very serious with treatment in 32% patients.

Table 1. Comparative representation of differences in the incidence of undesirable symptoms of nervousness and anxiety in a relation to the intensity of a problems that these undesirable symptoms present in all subjects, according to the Toronto scale (n = 508).

Frequency of the symptom No (%) Intensity of the problem No (%) P
Nervousness X2=623.387
never 43 ( 9) not a problem 79 (16) 0.001
rarely 99 (19) insignificant 109 (20)
sometimes 168 (33) moderate 139 (27)
often 143 (28) significant 112 (22)
daily 55 (10) severe 76 (15)
Anxiety, fear X2=155.790
never 47 (9) not a problem 80 (16) 0.001
rarely 102 (20) insignificant 111 (22)
sometimes 172 (34) moderate 147 (29)
often 131 (26) significant 112 (22)
daily 56 (11) severe 58 (11)
Shaky hands X2=902. 868
never 161 (32) not a problem 203 (40) 0.001
rarely 140 (28) insignificant 121 (24)
sometimes 110 (22) moderate 87 (17)
often 61 (12) significant 42 (8)
daily 36 (7) severe 55 (11)
Muscle spasm X2=887. 215
never 179 (35) not a problem 230 (45) 0.001
rarely 148 (30) insignificant 123 (24)
sometimes 103 (20) moderate 85 (17)
often 62 (12) significant 42 (8)
daily 16 (3) severe 28 (6)

Table 2. Comparative representation of differences in the incidence of increased or decreased appetite as a side effect of antidepressants in relation to the intensity of the problems which these side effects present in all subjects according to the Toronto Side Effects Scale (n= 508).

Frequency of the symptom No (%) Intensity of the problem No (%) P
Decreased appetite X2=643.637
never 185 (36) not a problem 256 (50) 0.001
rarely 91 (18) insignificant 84 (17)
sometimes 120 (24) moderate 77 (15)
often 63 (12) significant 46 ( 9)
daily 49 (10) severe 45 ( 9)
Increased appetite X2=1047.579
never 221 (44) not a problem 274 (54) 0.001
rarely 129 (25) insignificant 105 (20)
sometimes 90 (18) moderate 65 (13)
often 49 (10) significant 40 (8)
daily 19 (4) severe 24 (5)

In the total sample, the highest number of subjects (141 = 27%) were treated with Paroxetine; with Sertaline 90 (17%); with Flusetin 116 (22%), with Escitalopram or with an other antidepressant 107 (21%); and with Fluzepam 65 (13%) of subjects.X2 = 828,905 P <0.000. Previously, subjects were treated with Paroxetine (32%: 37% vs. 169: 141) significantly more frequently, and they were significantly less frequently treated with Sertalin ( 9%: 17% vs. 48:90) and Flusetin 17%: 22% (P = 0.001).

Side effects of antidepressants that occur often and on daily basis are: gastrointestinal problems (in 17% of subjects), indigestion (22%), nausea (18%), diarrhea (9%) and constipation (11%). As a significant problem, abdominal pain is felt by 14% of subjects, indigestion by 19% of subjects, nausea by 15% of subjects, diarrhea by 9% of subjects, and constipation by 11% of subjects.

Somatic side effects of antidepressants with often and daily occurrence are: tiredness in 45% of subjects (a high frequency); dizziness (24%); hypotension (15%); headache (34%); and blurred vision (22% of subjects). As a significant problem 40% of subjects feel tiredness; dizziness (25%); hypotension (15%); headache (34%); and blurred vision (22%).

Somatic side effects of antidepressants related to hormone dysregulation that occur often and on daily basis are: sweating in 34%; a sudden heat stroke in 22%; swelling in 8%; and dry mouth in 25% of subjects. As a significant problem in 29% of subjects occur sweating; in 20% a sudden heat stroke; in 10% swelling; and in 23% of them dry mouth. The frequency of side effects in relation to how do they present a problem to subjects in their daily life and activities is statistically significant (P<0.000).

Occurrence of tiredness is most frequent in treatment with Paroxetine (50%) and Flusetin (48%), but differences in the incidence of this side effect among the 5 most prescribed antidepressants are not significant. This side effect is most common in a treatment of a first recurrent episode of depression. It is significantly related to the duration of the treatment statistically (P=0.008) and it has a growing trend over time (P <0.001).

5. DISCUSSION

A treatment with antidepressants has often a potential risk of side effects and suicidal thoughts (16, 17). Although Selective Serotonin Reuptake Inhibitors (SSRIs) do have better overall safety and tolerability comparing to older antidepressants, experience and clinical trials have shown a significant incidence of their side effects.

Ferguson has investigated the causes of various side effects profiles, especially the causes of sexual dysfunction, weight gain, and sleep disorders. An occurence of side effects in long-term SSRI therapy is most concerning. Ferguson’s results comply with ours. The statistically significant side effects of SSRI antidepressants in correlation with the duration of the treatment in our subjects are: perception of increased sleep (0.039) as well as decreased sleep (P = 0.009), sweating (P <0.001), sudden heat stroke (P <0.001), being without orgasm (P = 0.004), decreased libido (P <0.001), weight loss (P = 0.045).

In clinical studies it has been confirmed that SSRIs have significantly less side effects compared to Tricyclic Antidepressants (TCA) (19). They do not cause irregularities in cardiac conduction or rhythm disturbances in case of an overdose (20). As confirmed in our study, Selective Serotonin Reuptake Inhibitors (SSRIs) are currently the first choice of therapy for depression (17).

In a prospective control study which included 1251 patients, in the treatment of depression 659 of them have used sertraline and 592 of others have used SSRIs (paroxetine, fluoxetine, or fluvoxamine) for at least 12 months. A significant side effect in patients treated with Sertraline compared to patients treated with other SSRI antidepressants is diarrhea (14% vs.. 6.8%), P <0.05 (21). Our results are contradictory. In our study, tiredness occurred most commonly in treatment with Paroxetine (50%) and Flusetin (48%), but differences in the prevalence of this side effect among the five most prescribed antidepressants were not significant. Headache most frequently occurs in treatment with Flusetin (39%), just as well as dizziness (30%); blurred vision (26%), and dry mouth occur in treatment with Paroxetin. However, the differences for all known SSRI side effects are not significant.

6. CONCLUSION

It is necessary to educate the patient about the nature and properties of the depressive disorder, and to introduce him to the expected course of recovery, as well as the need to adhere to the recommended therapy and the possible side effects of the drug. The results of our research have shown an important degree of variability in side effects of the most commonly prescribed SSRI antidepressants compared to those reported in clinical trials, which had been monitored before they were approved.

Declaration of Patient Consent:

The authors certify that they obtained all appropriate patient consent forms.

Authors contribution:

Each author equally participated in preparation of this article. Final proof reading was made by the first author.

Conflict of interest:

None declared.

Financial support and sponsorship

Nil.

REFERENCES

  • 1.Nelson JC, Devanand DP. A systematic review and metha analysis of placebo controlled antidepressant studies in people with depression and dementia. Journal of American Geriatric Society. 2011;59(3):203–210. doi: 10.1111/j.1532-5415.2011.03355.x. [DOI] [PubMed] [Google Scholar]
  • 2.Parker G. Differential effectiveness of newer and older antidepressants appears mediated by an age effect on the phenotype expression of depression. Acta Psychiatr Scand. 2002;106(3):168–170. doi: 10.1034/j.1600-0447.2002.02432.x. [DOI] [PubMed] [Google Scholar]
  • 3.Sutherland JE, Sutherland AJ, Hoehns D. Achieving the best outcome in tretment of depression. Journal of Family Practice. 2003;59(3):203–210. [PubMed] [Google Scholar]
  • 4.Gilbody S, Whitty P, Grimshaw J, Thomas R. Educational and organisational interventions to improve the managment of depression in primary care: a systematic review. JAMA. 2003;289(23):3145–3151. doi: 10.1001/jama.289.23.3145. [DOI] [PubMed] [Google Scholar]
  • 5.Turner EH, Matthews AM, Linardatos E, Tell A, Rosenthal R. Selective publication of antidepressant trials and its influence on apparent efficiacy. N Engl J Med. 2008;358(3):252–260. doi: 10.1056/NEJMsa065779. [DOI] [PubMed] [Google Scholar]
  • 6.Bymaster FP, Zhang W, Carter PA, Shaw J, Chernet E, et al. Fluoxetine, but not other selective serotonin uptake inhibitors, increases norepinephrine and dopamine extracellular levels in prefrontal cortex. Psychopharmacology. 2002;160(4):353–361. doi: 10.1007/s00213-001-0986-x. [DOI] [PubMed] [Google Scholar]
  • 7.Dalfen AK, Stewart DE. Who develops severe or fatal drug reactions to selective serotonin reuptake inhibitors? Can J Psychiatry. 2001;46(3):258–263. doi: 10.1177/070674370104600306. [DOI] [PubMed] [Google Scholar]
  • 8.Montejo AL, Llorka G, Izquiriedo JA, Rico-Villademoros F. Incidence of sexual disfunction associated with antidepressant agents: A prospective multicenter study of 1022 outpatients. J Clin Psychiatry. 2001;62(3):10–21. [PubMed] [Google Scholar]
  • 9.Wagstaff AJ, Cheer SM, Matheson AJ, Ormrod D, Goa KL. Paroxetine: An update of its use in psychiatric disorders in adults. Drugs. 2002;62(4):655–703. doi: 10.2165/00003495-200262040-00010. [DOI] [PubMed] [Google Scholar]
  • 10.Sampson SM. Treating depression with selective serotonin reuptake inhibitors: a practical approach. Mayo Clin Proc. 2001;76:739–744. doi: 10.4065/76.7.739. [DOI] [PubMed] [Google Scholar]
  • 11.Wallace M. Real progress: The patient’s perspective. International Clinical Psychopharmacology. 2001;16(1):S21–S24. doi: 10.1097/00004850-200101001-00005. [DOI] [PubMed] [Google Scholar]
  • 12.Hamilton M. A rating scale for depression. J Neurol Neurosurg Psychiatry. 1960;23:56–62. doi: 10.1136/jnnp.23.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Vanderkooy JD, Sidney H, Kennedy MD, Michael-Bagby R. Antidepressant Side Effects in Depression Patients Treated in Naturalistic Setting: A study of Bupropion, Moclobemide, Paroxetine, Sertaline, and Venflaxine. W Can J Psychatry. 2002;47(2):174–180. doi: 10.1177/070674370204700208. [DOI] [PubMed] [Google Scholar]
  • 14.Healy D. Harcourt Brace and Jovanoviten. 2. New York: 2001. Psychiatric drugs explained. [Google Scholar]
  • 15.Dewan MJ, Anand VS. Evaluating and tolerability of the new antidepressants. J Nerv Ment Dis. 1999;187:96–101. doi: 10.1097/00005053-199902000-00005. [DOI] [PubMed] [Google Scholar]
  • 16.Kupfer DJ, Frank E, Phillips ML. Major depressive disorder: new clinical, neurobiological, and treatment perspectives. Lancet. 2012;379:1045–1049. doi: 10.1016/S0140-6736(11)60602-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Cuijpers P, Dekker J, Hollon SD, Andersson G. Adding psychotherapy to pharmacotherapy in the treatment of depressive disorders in adults: a meta-analysis. J Clin Psychiatry. 2009;70:1219–1224. doi: 10.4088/JCP.09r05021. [DOI] [PubMed] [Google Scholar]
  • 18.Ferguson JM. Antidepressant Medications: Adverse effects and tolerability. Prim Care Companion J Clin Psych. 2001;3(1):22–27. doi: 10.4088/pcc.v03n0105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Edwards JG, Anderson I. Systematic review and guide to selection of selective serotonin reuptake inhibitors. Drugs. 1999;58(6):1207–1209. doi: 10.2165/00003495-199957040-00005. [DOI] [PubMed] [Google Scholar]
  • 20.Feighner JP. Mechanism of action of antidepressant medication. J Clin Psychiatry. 1999;60(4):4–11. [PubMed] [Google Scholar]
  • 21.DeWilde J, Spiers R, Martens C, et al. A double- blind, comparative, multicentre study comparing Paroxetine with Fluoxetine in depressed patients. Acta Psychiatr Scand. 1993;87:141–145. doi: 10.1111/j.1600-0447.1993.tb03345.x. [DOI] [PubMed] [Google Scholar]

Articles from Materia Socio-Medica are provided here courtesy of The Academy of Medical Sciences of Bosnia and Herzegovina

RESOURCES