New Classification of Selective Serotonin Reuptake Inhibitor Withdrawal
Open accessAbstract
inal symptoms at the same intensity as before treatment, entailing a return of the same episode and a new episode of illness, respectively [6, 9] . When treatment with a CNS drug is discontinued, patients can experience classic new withdrawal symptoms, rebound and/or persistent postwithdrawal disorders, or relapse/recurrence of the original illness [6, 9, 14] . New and rebound symptoms can occur for up to 6 weeks after drug withdrawal, depending on the drug elimination half-life [2, 3] , while persistent postwithdrawal or tardive disorders associated with longlasting receptor changes may persist for more than 6 weeks after drug discontinuation. Initial withdrawal symptoms from CNS drugs have been reported to be more frequent and severe when high-potency drugs and drugs with a short elimination half-life have been used [9, 10] . CNS drugs with a shorter elimination half-life and rapid onset of action also carry a higher risk of dependency and high-dose use [9, 10] . Withdrawal symptoms can be relatively short-lasting, lasting for a few hours to a few weeks with complete recovery, while others may persist and last for several months [1, 15, 16] . Fava et al. [1] have proposed using the terminology ‘withdrawal syndrome’ to replace the term ‘discontinuation syndrome’, which has been most often used to describe SSRI withdrawal. They have recommended the Selective serotonin reuptake inhibitors (SSRIs) are widely used in clinical practice, and have advanced the treatment of depressi…
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 118 cited sources checked · 0 supported · 0 flagged
- Findingown data
In a 50-year-old woman with social phobia treated with citalopram 20 mg/day for 5 years for an MDE, tapering and discontinuation of citalopram produced new withdrawal symptoms (sweating, agitation, nausea) for 2 weeks.
“After the discontinuation of citalopram, she reported new symptoms, such as sweating, agitation, and nausea, for 2 weeks.”
Quote in the paperSubstantial claim - Findingown data
The same patient developed an MDE with melancholic features (deep anhedonia, depressed mood with diurnal variation, loss of energy, guilt, and suicidal thoughts) that she had never had before.
“However, she also developed MDE with melancholic features accompanied by deep anhedonia, depressed mood with diurnal variation, loss of energy, guilt, and suicidal thoughts, which she had never had before.”
Quote in the paperSubstantial claim - Premisecitation
Some initial new withdrawal symptoms common to all CNS drug classes include nausea, headaches, tremor, sleep disturbances, decreased concentration, anxiety, irritability, agitation, aggression, depression, or dysphoria.
“Some initial new withdrawal symptoms common to all CNS drug classes include nausea, headaches, tremor, sleep disturbances, decreased concentration, anxiety, irritability, agitation, aggression, depression, or dysphoria.”
Quote in the paperSubstantial claim - Premisecitation§ New Classification of Selective Serotonin Reuptake Inhibitor Withdrawal
Withdrawal from SSRIs and other CNS drugs produces psychiatric symptoms that can be confounded with true relapse or recurrence of the original illness.
“Withdrawal from SSRIs and other CNS drugs produces psychiatric symptoms that can be confounded with true relapse or recurrence of the original illness [1,2,7] .”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
High potency and short and intermediate half-life compounds tend to carry greater risks for withdrawal symptoms, in addition to drug dependence.
“High potency and short and intermediate half-life compounds tend to carry greater risks for withdrawal symptoms, in addition to drug dependence [6,9,10] .”
Quote in the paperNot a substantial claim0 of 3 sources checked
- Premisecitation
A recurrent disabling withdrawal symptom described in the literature and online by patients is a sensory symptom of electric shock sensations and electric-like waves.
“A recurrent disabling withdrawal symptom described in the literature and online by patients is a sensory symptom of electric shock sensations and electric-like waves [1,12,22,26] .”
Quote in the paperNot a substantial claim0 of 4 sources checked - Premisecitation
New withdrawal symptoms described in the literature include flu-like symptoms, headaches, nausea, diarrhea, dizziness, decreased concentration, sleep disturbances, dysphoria, irritability, and restlessness.
“New withdrawal symptoms described in the literature include flu-like symptoms, headaches, nausea, diarrhea, dizziness, decreased concentration, sleep disturbances, dysphoria, irritability, and restlessness [1,12,22] .”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
New withdrawal symptoms are common to all CNS drugs, including opioids, barbiturates, alcohol, antidepressants, antipsychotics, and benzodiazepines.
“They are common to all CNS drugs, including opioids, barbiturates, alcohol, antidepressants, antipsychotics, and benzodiazepines [5,10,11] .”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
The appearance or onset of withdrawal symptoms depends on the duration of action; short-acting drugs have an early peak of onset.
“The appearance or onset of withdrawal symptoms depends on the duration of action; for example, short-acting drugs have an early peak of onset [10] .”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [10] source
Not checked in the free run.
- Interpretationcitation
Specific serotonin-related symptoms during SSRI withdrawal include diarrhea, flu-like symptoms, dizziness, myoclonus, electric shock sensations, and premature ejaculation.
“These specific serotonin-related symptoms include diarrhea, flu-like symptoms, dizziness, myoclonus, electric shock sensations, and premature ejaculation.”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation§ New Classification of Selective Serotonin Reuptake Inhibitor Withdrawal
Existing checklists such as the Discontinuation-Emergent Signs and Symptoms (DESS) and criteria for SSRI withdrawal symptoms do not differentiate between different types of withdrawal.
“Existing checklists, such as the Discontinuation-Emergent Signs and Symptoms (DESS) [20] , and criteria for SSRI withdrawal symptoms [12,21] do not differentiate between different types of withdrawal.”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
New SSRI withdrawal symptoms have been found to occur after drug discontinuation with variable frequency and duration, depending on the SSRI which is discontinued.
“New SSRI withdrawal symptoms have been found to occur after drug discontinuation with variable frequency and duration, depending on the SSRI which is discontinued [1,12,22] .”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
The prevalence of rebound is greater among patients taking benzodiazepines with short to intermediate half-lives than among those taking agents with long half-lives.
“The prevalence of rebound is greater among patients taking benzodiazepines with short to intermediate half-lives (e.g.triazolam, lorazepam, and alprazolam) than among those taking agents with long half-lives [9,14] .”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisenone given
When previous drug treatment is not restarted, postwithdrawal disorders may last for several months to years.
“When the previous drug treatment is not restarted, postwithdrawal disorders may last for several months to years.”
Quote in the paperSubstantial claim - Premisecitation
New withdrawal symptoms, measured using the DESS, also appeared after paroxetine and sertraline discontinuation.
“New withdrawal symptoms, measured using the DESS, also appeared after paroxetine and sertraline discontinuation.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [20] source
Not checked in the free run.
- Premisecitation
The reinforcing properties of short-acting and short-elimination half-life CNS drugs appear to be the same for all CNS drug classes.
“The reinforcing properties of short-acting and short-elimination half-life CNS drugs appear to be the same for all CNS drug classes [6,9] .”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
There is increasing evidence for postwithdrawal disorders with SSRI long-term use.
“We now have increasing evidence for postwithdrawal disorders with SSRI long-term use [6,15,16,26,37] .”
Quote in the paperSubstantial claim0 of 5 sources checked - Premisecitation
In that study, patients taking sertraline (n=34) and those taking fluoxetine (n=37) did not have rebound depression.
“Pa-tients taking sertraline (n = 34) and those taking fluoxetine (n = 37) did not have rebound depression.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [34]
Not checked in the free run.
- Premisecitation
Rebound with short-acting drugs may be best illustrated by withdrawal from cocaine and heroin, which both have a rapid onset and brief duration of action.
“Rebound with short-acting drugs may be best illustrated by withdrawal from cocaine and heroin, which both have a rapid onset and brief duration of action [10,23] .”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Short-acting antipsychotics such as clozapine and quetiapine, which have fast dissociation from dopamine D2 receptor, have been shown to have a greater risk of rebound.
“This is also true for short-acting antipsychotics, such as clozapine and quetiapine, which have a fast dissociation from do- pamine D 2 receptor, and have been shown to have a greater risk of rebound [6,33] .”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [6] source
Not checked in the free run.
- cites [33]
Not checked in the free run.
- Interpretationcitation
Examination of various studies shows that rebound withdrawal occurs with SSRIs as well as with other CNS drugs.
“However, examination of various studies [20,34,35] shows us that this type of withdrawal occurs with SSRIs as well as with other CNS drugs.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [20] source
Not checked in the free run.
- cites [34]
Not checked in the free run.
- cites [35]
Not checked in the free run.
- Premisecitation
Severity of new SSRI withdrawal symptoms may vary mainly according to the SSRI used.
“Severity may also vary mainly according to the SSRI used [1,20] .”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Persistent postwithdrawal disorders or tardive receptor supersensitivity disorders have been described with the use of antipsychotic medication.
“Persistent postwithdrawal disorders or tardive receptor supersensitivity disorders have been described with the use of antipsychotic medication [7,17,18] .”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
Rosenbaum et al. demonstrated rebound major depression, although not described as such, in a double-blind withdrawal trial (5-8 days) in 242 patients with major depression who had maintenance paroxetine, sertraline or fluoxetine treatment interrupted.
“Rosenbaum et al. [20] demonstrated rebound major depression, although the authors did not describe it as such, in a double-blind withdrawal trial (5-8 days) conducted in 242 patients with major depression who had their maintenance paroxetine, sertraline or fluoxetine treatment interrupted [20] .”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [20] source
Not checked in the free run.
- Premisecitation
The high risk of disabling withdrawal with paroxetine is thought to be related to noradrenergic and cholinergic supersensitivity.
“thought to be related to noradrenergic and cholinergic supersensitivity [15,35]”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [15] source
Not checked in the free run.
- cites [35]
Not checked in the free run.
- Premisecitation
The most frequent persistent postwithdrawal disorder symptoms reported online were disturbed mood, depression, emotional liability, mood swings, irritability, anxiety, insomnia, impaired concentration, and impaired memory.
“The most frequent persistent postwithdrawal disorder symptoms reported online were disturbed mood, depression, emotional liability, mood swings, irritability, anxiety, insomnia, impaired concentration, and impaired memory.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [26] source
Not checked in the free run.
- Premisecitation
According to most studies, even with gradual tapering, withdrawal symptoms still occur.
“According to most studies [1,15,16,20,29] , even with gradual tapering, withdrawal symptoms still occur.”
Quote in the paperSubstantial claim0 of 5 sources checked - Premisecitation
Paroxetine has an earlier steady-state concentration (7-14 days) compared with fluoxetine (28-35 days).
“earlier steady-state concentration (7-14 days for paroxetine compared with 28-35 days with fluoxetine) [35]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [35]
Not checked in the free run.
- Premisecitation
Paroxetine has a shorter half-life (19 h) compared with fluoxetine (45 h).
“its shorter half-life (19 h compared with 45 h for fluoxetine)”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [35]
Not checked in the free run.
- Premisecitation
Paroxetine carries a high risk of disabling withdrawal.
“Given the evidence for the high risk of disabling withdrawal with paroxetine”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [15] source
Not checked in the free run.
- cites [35]
Not checked in the free run.
- Interpretationnone given
Gradual tapering, rather than abrupt discontinuation, can help control the severity of withdrawal symptoms.
“However, gradual tapering, rather than abrupt discontinuation, can help to control the severity of withdrawal symptoms.”
Quote in the paperSubstantial claim
- May combine two claims. 29
- Classified as probably not a substantial claim. 14
May combine two claims.
Findingown dataIn that patient, the melancholic depression persisted for an additional week while other withdrawal symptoms disappeared.
“The patient was observed for an additional week, and while other withdrawal symptoms disappeared, the melancholic depression persisted.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataCase 1 illustrates a persistent postwithdrawal disorder with generalized anxiety disorder, which responded to CBT and clonazepam, but without complete recovery, still requiring clonazepam despite completion of CBT.
“This case illustrates a persistent postwithdrawal disorder with GAD, which responded to CBT and clonazepam, but without complete recovery, still requiring clonazepam despite the completion of the CBT.”
Quote in the paperNot a substantial claim- Rests on an assumption: The three types of withdrawal (new withdrawal symptoms, rebound, and persistent postwithdrawal disorders) are distinct and can be reliably differentiated from relapse or recurrence of the original illness using the proposed criteria.
May combine two claims.
Findingown dataCase 2 illustrates a persistent postwithdrawal cyclothymic disorder that developed after paroxetine discontinuation and lasted 3 years, with remission but without complete recovery.
“Subsequently, he developed significant cyclothymic disorder, with greatly increased reactivity to environmental stimuli and anxious distress, which lasted for 3 years.”
- Also stated in: § Case 2: Persistent Postwithdrawal Cyclothymic Disorder A 37-year-old man was treated for panic disorder with agoraphobia with paroxetine 20 mg/day for 7 years.Panic disorder and agoraphobia persisted despite treatment, and any attempt to reduce paroxetine was unsuccessful.He could only leave the house to go to work, and limited his activities to what he could not refuse for work, declining any other outings for leisure, including out-of-town opportunities.When the patient sought a new consultation, he was first treated for agoraphobia with CBT.A specialized psychologist guided him with homework exposure, consisting of 10 sessions every other week.His agoraphobia improved, and a paroxetine taper was then initiated.It was first tapered to 10 mg nightly, which immediately resulted in nervousness, headache, tension, and diarrhea.After 1 week of this paroxetine dose reduction, the patient was switched to fluoxetine 20 mg/day, which resulted in new withdrawal symptoms.After 2 months, these new symptoms improved, and fluoxetine was tapered to 10 mg/day for 1 week and then discontinued.Subsequently, he developed significant cyclothymic disorder, with greatly increased reactivity to environmental stimuli and anxious distress, which lasted for 3 years.It is important to note that he had no previous history of mood disorder.He was prescribed clonazepam without a decrease in his symptoms.Three years after the discontinuation of paroxetine, the patient started to improve, and the postwithdrawal cyclothymic disorder remitted, but without complete recovery. · plain
“Three years after the discontinuation of paroxetine, the patient started to improve, and the postwithdrawal cyclothymic disorder remitted, but without complete recovery.”
Quote in the paperSubstantial claim- Rests on an assumption: The three types of withdrawal (new withdrawal symptoms, rebound, and persistent postwithdrawal disorders) are distinct and can be reliably differentiated from relapse or recurrence of the original illness using the proposed criteria.
- Also stated in: § Case 2: Persistent Postwithdrawal Cyclothymic Disorder A 37-year-old man was treated for panic disorder with agoraphobia with paroxetine 20 mg/day for 7 years.Panic disorder and agoraphobia persisted despite treatment, and any attempt to reduce paroxetine was unsuccessful.He could only leave the house to go to work, and limited his activities to what he could not refuse for work, declining any other outings for leisure, including out-of-town opportunities.When the patient sought a new consultation, he was first treated for agoraphobia with CBT.A specialized psychologist guided him with homework exposure, consisting of 10 sessions every other week.His agoraphobia improved, and a paroxetine taper was then initiated.It was first tapered to 10 mg nightly, which immediately resulted in nervousness, headache, tension, and diarrhea.After 1 week of this paroxetine dose reduction, the patient was switched to fluoxetine 20 mg/day, which resulted in new withdrawal symptoms.After 2 months, these new symptoms improved, and fluoxetine was tapered to 10 mg/day for 1 week and then discontinued.Subsequently, he developed significant cyclothymic disorder, with greatly increased reactivity to environmental stimuli and anxious distress, which lasted for 3 years.It is important to note that he had no previous history of mood disorder.He was prescribed clonazepam without a decrease in his symptoms.Three years after the discontinuation of paroxetine, the patient started to improve, and the postwithdrawal cyclothymic disorder remitted, but without complete recovery. · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataIn that patient, after 2 years, attempts to taper nortriptyline and clonazepam (one at a time) were unsuccessful.
“After 2 years, she is still on nortriptyline 100 mg/day and clonazepam 0.5 mg three times a day.Any attempt to taper both drugs (one at the time) has been unsuccessful.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationOther new withdrawal symptoms more specific to a certain class of CNS drugs include lacrimation, rhinorrhea, and sneezing for opiates, paroxysmal sweats for alcohol, and increased appetite for nicotine.
“Other new withdrawal symptoms that may be more specific to a certain class of CNS drugs include lacrimation, rhinorrhea, and sneezing for opiates, paroxysmal sweats for alcohol, and increased appetite for nicotine [10,23,24] .”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationMajor complications of withdrawal may occur, such as seizures, suicide and psychoses, and in cases of barbiturate or alcohol abuse, even death.
“However, major complications of withdrawal may occur, such as seizures, suicide and psychoses [10] , and, in cases of barbiturate or alcohol abuse, even death [25] .”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Premisecitation§ New Classification of Selective Serotonin Reuptake Inhibitor WithdrawalDifferent types of withdrawal syndromes described with SSRIs and other CNS drug classes include new withdrawal symptoms, rebound, and persistent postwithdrawal disorders.
“Different types of syndromes have been described with the withdrawal from SSRIs and other CNS drug classes, including benzodiazepines, antipsychotics, antidepressants, opiates, barbiturates, and alcohol: (1) new withdrawal symptoms (classic withdrawal symptoms from CNS drugs) [1,[4][5][6][9][10][11][12] , (2) rebound [2,6,9,[13][14][15][16] , and (3) persistent postwithdrawal disorders [7,17,18] (”
Quote in the paperSubstantial claim0 of 5 sources checkedMay combine two claims.
Premisecitation§ New Classification of Selective Serotonin Reuptake Inhibitor WithdrawalFava et al.'s systematic review of SSRI withdrawal analyzed 23 studies (15 randomized controlled studies, 4 open trials, 4 retrospective investigations) and 38 case reports, and found both early and late onset, and short and long duration of withdrawal symptoms.
“Recently, Fava et al. [1] have conducted the first systematic review of SSRI withdrawal.The authors analyzed 23 studies (15 randomized controlled studies, 4 open trials, 4 retrospective investigations) and 38 case reports of SSRI withdrawal, and found both early and late onset, and short and long duration of withdrawal symptoms.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Fava et al. [1] source
Not checked in the free run.
May combine two claims.
Interpretationnone given§ New Classification of Selective Serotonin Reuptake Inhibitor WithdrawalSSRI withdrawal symptoms occur when the drug's pharmacological effects diminish after drug decrease or discontinuation, indicating an underlying pharmacological mechanism comparable to that of other CNS drug withdrawal symptoms.
“SSRI withdrawal symptoms occur when the drug's pharmacological effects diminish after drug decrease or discontinuation, which indicates an underlying pharmacological mechanism comparable to that of other CNS drug withdrawal symptoms.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationThese withdrawal symptoms are typically transient, reversible and usually last less than 6 weeks, depending on the drug elimination half-life.
“These symptoms are typically transient, reversible and usually last <6 weeks, depending on the drug elimination half-life [2,[9][10][11] .”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [2,[9][10][11]
Not checked in the free run.
May combine two claims.
PremisecitationNew SSRI withdrawal symptoms usually reach a peak of onset between 36 and 96 h after SSRI reduction or discontinuation, and are reversible, lasting from a few hours up to 6 weeks.
“They usually reach a peak of onset between 36 and 96 h after SSRI reduction or discontinuation, and are reversible, lasting from a few hours up to 6 weeks [1,12,22] .”
Quote in the paperSubstantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationNew withdrawal symptoms reported with SSRIs include a wide range of symptoms, both physical and psychological, and are found throughout different systems in the body.
“New withdrawal symptoms reported with SSRIs include a wide range of symptoms, both physical and psychological [1] , and are found throughout different systems in the body ( table 2 ).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [1] source
Not checked in the free run.
May combine two claims.
PremisereasoningDifferent classes of CNS drugs may share common withdrawal symptoms, but may also have their own specific withdrawal symptoms.
“Different classes of CNS drugs may share common withdrawal symptoms, but may also have their own specific withdrawal symptoms.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationTardive dyskinesia and supersensitivity psychosis are well-known postwithdrawal disorders (also called supersensitivity syndromes).
“Tardive dyskinesia and supersensitivity psychosis are well-known postwithdrawal disorders (also called supersensitivity syndromes) [7,17,18] .”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationRebound insomnia was demonstrated in individuals with insomnia upon withdrawal of short and intermediate half-life benzodiazepines, and early morning insomnia with rapidly eliminated benzodiazepines.
“These reports were followed by the demonstration of rebound insomnia in individuals with insomnia upon withdrawal of short and intermediate half-life benzodiazepines [13] and early morning insomnia with rapidly eliminated benzodiazepines [32] .”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [13] source
Not checked in the free run.
- cites [32]
Not checked in the free run.
Classified as probably not a substantial claim.
Premisenone givenDue to the lack of classification for SSRI withdrawal, rebound symptoms in SSRI withdrawal have not been described as such in the literature.
“Due to the lack of classification for SSRI withdrawal, rebound symptoms in SSRI withdrawal have not been described as such in the literature.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationData from controlled trials, case reports, and online patient reports show that paroxetine is most likely to be associated with new withdrawal symptoms, and fluoxetine the least.
“Data from controlled trials [15,20,29] , case reports [16] , and online patient reports [26] show that paroxetine is most likely to be associated with new withdrawal symptoms, and fluoxetine the least.”
Quote in the paperSubstantial claim0 of 5 sources checkedMay combine two claims.
Premisenone givenIt has been clearly demonstrated with benzodiazepines that patients often respond rapidly to the reinstitution of the drug, which may lead to a false sense of efficacy and need for the drug.
“It has been clearly demonstrated with benzodiazepines that patients often respond rapidly to the reinstitution of the drug, which may lead to a false sense of efficacy and need for the drug.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningIn the Rosenbaum et al. and the other study, drug interruption was short (5-8 days), and it is unlikely that rebound with fluoxetine would be seen; as fluoxetine has a long half-life, it is also less likely to cause rebound.
“In this study and the study by Rosenbaum et al. [20] , the drug interruption was short (5-8 days), and it is unlikely that rebound with fluoxetine would be seen.However, as fluoxetine has a long half-life, it is also less likely to cause rebound.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [20] source
Not checked in the free run.
May combine two claims.
PremisecitationIn Rosenbaum et al.'s study, patients taking paroxetine and sertraline developed worsened depressive symptoms on the Hamilton Depression Rating Scale and Montgomery-Asberg Depression Rating Scale after treatment interruption, and returned to baseline depression measurements after reinstitution of treatment.
“In this study, patients taking paroxetine and sertraline developed worsened depressive symptoms on the Hamilton Depression Rating Scale and Montgomery-Asberg Depression Rating Scale after treatment interruption, and returned to baseline depression measurements after reinstitution of the treatment.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [20] source
Not checked in the free run.
May combine two claims.
PremisecitationRebound anxiety and rebound panic were reported with abrupt benzodiazepine discontinuation.
“Rebound anxiety [2,14] and rebound panic [15] were then reported with abrupt benzodiazepine discontinuation [9] .”
Quote in the paperNot a substantial claim0 of 4 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationCNS drug rebound was first reported as REM rebound, consisting of an increase in REM sleep following abrupt withdrawal of barbiturates and nonbenzodiazepine hypnotics.
“CNS drug rebound was first reported as REM rebound, consisting of an increase in REM sleep following abrupt withdrawal of barbiturates and nonbenzodiazepine hypnotics [30,31] .”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [30] source
Not checked in the free run.
- cites [31]
Not checked in the free run.
May combine two claims.
PremisecitationPersistent postwithdrawal disorders have been described with different classes of CNS drugs (e.g. protracted insomnia for alcohol and benzodiazepine withdrawal and major depression/dysphoria for cocaine and amphetamine withdrawal), and even more so with specific drugs (e.g. quetiapine and paroxetine) within a drug class.
“Persistent postwithdrawal disorders have been described with different classes of CNS drugs (e.g.protracted insomnia for alcohol and benzodiazepine withdrawal [10,36] and major depression/dysphoria for cocaine and amphetamine withdrawal [10,23] ), and even more so with specific drugs (e.g.quetiapine and paroxetine) within a drug class [6,15,16,33] .”
Quote in the paperSubstantial claim0 of 7 sources checked- cites [10] source
Not checked in the free run.
- cites [36]
Not checked in the free run.
- cites [23] source
Not checked in the free run.
- cites [6] source
Not checked in the free run.
- cites [15] source
Not checked in the free run.
- cites [16] source
Not checked in the free run.
- cites [33]
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable), S4 (based). May combine two claims.
InterpretationreasoningDifferentiating withdrawal from relapse and recurrence of the original illness will allow clinicians to more effectively reduce and withdraw SSRIs, and find a minimal therapeutic dose.
“Differentiating withdrawal from relapse and recurrence of the original illness will allow clinicians to more effectively reduce and withdraw SSRIs, and find a minimal therapeutic dose.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Interpretationnone givenReducing the dose gradually develops a plateau period that can help distinguish the development of new withdrawal symptoms, rebound, or recurrent symptoms.
“Furthermore, by reducing the dose gradually, a plateau period develops that can help to distinguish the development of new withdrawal symptoms, rebound, or recurrent symptoms.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationChecklists such as the DESS are helpful to ensure that all new withdrawal symptoms are inquired about, particularly if the medication is withdrawn before 6 months of continuous intake.
“Checklists, such as the DESS [20] , are also helpful to ensure that all new withdrawal symptoms are inquired about, particularly if the medication is withdrawn before 6 months of continuous intake.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [20] source
Not checked in the free run.
May combine two claims.
PremisecitationSignificant postwithdrawal illnesses found with SSRI use include anxiety disorders, tardive insomnia, major depression, and bipolar illness.
“Significant postwithdrawal illnesses found with SSRI use include anxiety disorders, tardive insomnia, major depression, and bipolar illness.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based). May combine two claims.
Interpretationnone givenWithdrawal symptoms may occur with SSRIs, similarly to other CNS drugs, and they must be identified and differentiated from relapse and recurrence of the original illness.
“Withdrawal symptoms may occur with SSRIs, similarly to other CNS drugs, and they must be identified and differentiated from relapse and recurrence of the original illness.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationPostwithdrawal disorders may resemble rebound symptoms being more severe than the original symptoms, but these disorders persist at least 6 weeks in contrast to rebound symptoms.
“They may resemble rebound symptoms being more severe than the original symptoms, but these disorders persist at least 6 weeks in contrast to rebound symptoms and [6,15,16,26,37] .”
Quote in the paperSubstantial claim0 of 5 sources checkedMay combine two claims.
PremisecitationFava et al. conducted a study of gradual SSRI discontinuation in panic disorder and found that 9 of 20 patients (45%) experienced new withdrawal symptoms, and that 3 of the 9 (33%) patients treated with paroxetine had postwithdrawal disorders at 1 year of follow-up, including bipolar spectrum disorder (n=2) and major depressive disorder (n=1).
“Fava et al. [16] conducted a study of gradual SSRI discontinuation in panic disorder and found that 9 of 20 patients (45%) experienced new withdrawal symptoms, and that 3 of the 9 (33%) patients treated with paroxetine had postwithdrawal disorders at 1 year of follow-up, including bipolar spectrum disorder (n = 2) and major depressive disorder (n = 1).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [16] source
Not checked in the free run.
May combine two claims.
PremisecitationThere were online cases of persistent postwithdrawal disorders found after the discontinuation of paroxetine, citalopram, escitalopram, and fluvoxamine, but not sertraline or fluoxetine.
“There were online cases of persistent postwithdrawal disorders found after the discontinuation of paroxetine, citalopram, escitalopram, and fluvoxamine, but not sertraline or fluoxetine [26] .”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [26] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationOne proposed mechanism for the beneficial effects of using an anticonvulsant as an adjunct to an antipsychotic in schizophrenia is its antikindling effect.
“One proposed mechanism explaining the beneficial effects of using an anticonvulsant as an adjunct to an antipsychotic in schizophrenia is its antikindling effect [39,40] .”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [39]
Not checked in the free run.
- cites [40]
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable), S4 (based).
Interpretationnone givenThe proposed diagnostic criteria will assist in distinguishing between new withdrawal symptoms, rebound, and persistent postwithdrawal disorders, and relapse or recurrence of the illness.
“The proposed diagnostic criteria will assist in distinguishing between new withdrawal symptoms, rebound, and persistent postwithdrawal disorders, and relapse or recurrence of the illness.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationWe previously reported two types of persistent postwithdrawal psychiatric disorders (pathological gambling and generalized anxiety) with paroxetine that were treated successfully with specific cognitive behavioral therapy (CBT) and medications.
“We previously reported two types of persistent postwithdrawal psychiatric disorders (pathological gambling and generalized anxiety) with paroxetine that were treated successfully with specific cognitive behavioral therapy (CBT) and medications [37] .”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [37]
Not checked in the free run.
Probably not a substantial claim: may not pass S4 (based). May combine two claims.
Interpretationnone givenGradual withdrawal may reduce new withdrawal and rebound symptoms but may have no effect on persistent postwithdrawal disorders.
“Of note, it may be that gradual withdrawal reduces new withdrawal and rebound symptoms, but has no effect on persistent postwithdrawal disorders.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationPersistent postwithdrawal panic disorder has been shown to occur following withdrawal of paroxetine, and paroxetine has also been associated with other postwithdrawal disorders.
“Persistent postwithdrawal panic disorder [15,38] has been shown to occur following withdrawal of paroxetine, and paroxetine has also been associated with other postwithdrawal disorders [6,15,16] .”
Quote in the paperSubstantial claim0 of 4 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationIn another study, we analyzed online reports from individuals who described postwithdrawal disorders after SSRI discontinuation.
“In another study, we analyzed online reports from individuals who described postwithdrawal disorders after SSRI discontinuation [26] .”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [26] source
Not checked in the free run.
Probably not a substantial claim: may not pass S4 (based).
Interpretationnone givenThe proposed diagnostic criteria will permit the identification of three types of withdrawal associated with SSRIs.
“The proposed diagnostic criteria will permit the identification of three types of withdrawal associated with SSRIs.”
Quote in the paperNot a substantial claim
The paper relies on this without support.
The three types of withdrawal (new withdrawal symptoms, rebound, and persistent postwithdrawal disorders) are distinct and can be reliably differentiated from relapse or recurrence of the original illness using the proposed criteria.
“These types of withdrawal need to be differentiated from relapse and recurrence of the original illness.”
“Our proposed classification aims to improve the detection and management of SSRI withdrawal, differentiating it from relapse and recurrence of the original illness.”
The paper relies on this without support.
A minimum of 6 months of continuous SSRI use prior to reduction or discontinuation is necessary to establish the drug's pharmacologic effect well enough to differentiate withdrawal phenomena from relapse or recurrence.
“We deem this treatment duration requirement necessary, so that the pharmacologic effect of the drug is well established, allowing for differentiation between withdrawal phenomena and relapse or recurrence of the original illness.”
The paper relies on this without support.
Symptoms common to CNS drugs and specific symptoms related to serotonergic pharmacology can be used to classify SSRI withdrawal.
“We will derive a classification for SSRI withdrawal based on withdrawal symptoms common to different CNS drug classes and specific symptoms common to SSRIs and SNRIs.”
The paper relies on this without support.
After 2 years of maintenance treatment, many types of persistent postwithdrawal disorders may be observed.
“After 2 years of maintenance treatment, many types of persistent postwithdrawal disorders may be observed.”
The paper relies on this without support.
Lamotrigine has a depression-stabilizing effect.
“Lamotrigine may also be beneficial as an adjunctive therapy with SSRIs to treat depression as it has a depression-stabilizing effect.”
The paper relies on this without support.
Long-term receptor changes occur with SSRI maintenance treatment and can be minimized by low doses and adjunct treatments such as CBT.
“Giving low doses of SSRIs and decreasing the lengths of SSRI maintenance treatment by using adjunct treatments, such as CBT, should be considered whenever possible to try to minimize long-term receptor changes.”
The paper relies on this without support.
SSRI withdrawal is similar enough to alcohol, opiate, and benzodiazepine withdrawal that the same management principles apply.
“Third, the same principles recommended for the management of alcohol, opiate and benzodiazepine withdrawal should apply to SSRIs, including the use of long half-life drugs [9,10] , such as fluoxetine.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The literature distinguishes between acute withdrawal syndromes, including rebound disorders, and persistent post-acute withdrawal syndromes (PAWS), including persistent post-withdrawal disorders.
“The literature further distinguishes between two broad categories of withdrawal syndromes: acute withdrawal syndromes, including rebound disorders, and persistent post-acute withdrawal syndromes (PAWS), including persistent post-withdrawal disorders (Chouinard and Chouinard, 2015; Cosci and Chouinard, 2020; Lerner and Klein, 2019).”
From Post-acute withdrawal syndrome (PAWS) after stopping antidepressants: a systematic review with meta-narrative synthesis (2025) · cites this paper as Chouinard and Chouinard, 2015
The introduction proposes three types of SSRI withdrawal: new withdrawal symptoms, rebound, and persistent postwithdrawal disorders. The Rebound Symptoms and Postwithdrawal Disorders sections distinguish transient rebound symptoms from disorders lasting at least six weeks. The paper does not present these as two broad categories called acute withdrawal and PAWS, so that framing is not supported by this source. (LLM, conf=0.83)
Experimental — accuracy not yet measuredRelapse and recurrence have symptom severity as before drug treatment, while drug withdrawal produces greater severity.
“(2) symptom severity as before drug treatment, while drug withdrawal produces greater severity [10].”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
The introductory passage describes relapse and recurrence as a return of the original symptoms at the same intensity as before treatment. The “Rebound Symptoms” section says symptoms return at greater intensity, and “Postwithdrawal Disorders” describes greater intensity as one possible presentation. The claim overgeneralizes this distinction: the paper also identifies new withdrawal symptoms, which are not necessarily more severe versions of the original symptoms. (LLM, conf=0.86)
Experimental — accuracy not yet measuredRelapse and recurrence have gradual onset of the original symptoms and illness, while drug withdrawal produces acute, abrupt return.
“both relapse and recurrence have 2 clinical features different from withdrawal syndromes: (1) the gradual onset of the original symptoms and illness, while drug withdrawal produces acute, abrupt return”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
The introductory classification describes relapse and recurrence as a gradual return of the original symptoms, and the Rebound Symptoms section describes rebound as a rapid return. The claim overgeneralizes that rapid return to drug withdrawal as a whole; the paper distinguishes rebound from other withdrawal phenomena, which can have different onset patterns. No page number is available for these passages in our copy. (LLM, conf=0.85)
Experimental — accuracy not yet measuredBoth FGAs and SGAs have shown to trigger withdrawal at decrease, switch, or discontinuation.
“Since both FGAs and SGAs have shown to trigger withdrawal at decrease, switch, or discontinuation,”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
The 'New Withdrawal Symptoms' section says antipsychotics can cause withdrawal when a drug is decreased or discontinued, and the 'Rebound Symptoms' section gives clozapine and quetiapine as examples. The paper does not explicitly establish the claim for both first- and second-generation antipsychotics, or address withdrawal during switching. (LLM, conf=0.82)
Experimental — accuracy not yet measuredPersistent post-withdrawal tardive dyskinesia is characterized by a hyperkinetic, involuntary, purposeless movement disorder occurring after decrease, discontinuation, or switch of antipsychotics.
“Persistent post-withdrawal tardive diskinesia is characterized by a hyperkinetic, involuntary, and purposeless movement disorder [10] occurring after decrease, discontinuation, or switch of antipsychotics.”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
The Postwithdrawal Disorders section (page not provided) identifies tardive dyskinesia as a postwithdrawal disorder associated with antipsychotic medication. It does not describe the movements as hyperkinetic, involuntary, or purposeless, or specify that the disorder occurs after switching antipsychotics. (LLM, conf=0.83)
Experimental — accuracy not yet measured
Withdrawal from psychotropic medications can produce psychiatric symptoms often confounded with relapse or recurrence of the original illness.
“Withdrawal from psychotropic medications can produce psychiatric symptoms often confounded with relapse (i.e., a return of the same episode) or recurrence (i.e., a new episode) of the original illness [10].”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
One recently identified main concern is the potential for acute and persistent post-acute (protracted) withdrawal symptoms when the medication is discontinued.
“One recently identified main concern is the potential for acute and persistent post-acute (protracted) withdrawal symptoms when the medication is discontinued (Boland et al., 2024; Chouinard and Chouinard, 2015; Fava and Cosci, 2019; Hengartner et al., 2019; Lerner and Klein, 2019; Massabki and Abi-Jaoude, 2021).”
From Post-acute withdrawal syndrome (PAWS) after stopping antidepressants: a systematic review with meta-narrative synthesis (2025) · cites this paper as Chouinard and Chouinard, 2015
Compared to the steadily increasing number of editorials, commentaries and narrative reviews mentioning PAWS, the lack of high-quality original studies providing reliable evidence on the epidemiology and clinical management of PAWS is striking.
“Nevertheless, compared to the steadily increasing number of editorials, commentaries and narrative reviews mentioning PAWS (e.g. Chouinard and Chouinard, 2015; Davies et al., 2019; Fava and Belaise, 2018; Fava and Cosci, 2019; Lerner and Klein, 2019), the lack of high-quality original studies providing reliable evidence on the epidemiology and clinical management of PAWS is striking.”
From Post-acute withdrawal syndrome (PAWS) after stopping antidepressants: a systematic review with meta-narrative synthesis (2025) · cites this paper as Chouinard and Chouinard, 2015
Withdrawal symptoms do not necessarily wane after drug discontinuation and may build into persistent post-withdrawal disorders.
“Withdrawal symptoms do not necessarily wane after drug discontinuation and may build into persistent post-withdrawal disorders 98 .”
From The pursuit of euthymia (2020) · cites this paper as [98]
New withdrawal symptoms are usually the same and common to all psychotropic medications during withdrawal, but also specific and unique for a drug class.
“New symptoms are usually the same, common to all psychotropic medications during withdrawal [12, 15, 23] (e.g., nausea, headaches, sleep disturbances) [10], but also specific and unique for a drug class (e.g., specific serotonin-related symptoms: flu-like symptoms, diarrhea, confusion) [10].”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
Chouinard and Chouinard illustrated 3 cases of persistent post-withdrawal disorders: one had generalized anxiety disorder, one cyclothymic disorder, and one had major depressive episode with melancholic features.
“Finally, Chouinard and Chouinard [10] illustrated 3 cases of persistent post-withdrawal disorders: one had generalized anxiety disorder, one cyclothymic disorder, and one had major depressive episode with melancholic features.”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
After SSRIs long-term use, persistent post-withdrawal disorders have been described.
“After SSRIs long-term use, persistent post-withdrawal disorders have been described [10, 13, 18, 19, 112, 117, 118].”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
Rebound depression has been observed at a greater frequency with paroxetine or short-acting SSRIs.
“Rebound depression has been observed at a greater frequency with paroxetine or short-acting SSRIs [10, 13].”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
In two double-blind placebo studies, patients treated with paroxetine had acute return of pre-treatment symptoms, while patients taking fluoxetine did not.
“In both studies [111, 113], patients treated with paroxetine had acute return of pre-treatment symptoms [10, 111, 113], while patients taking fluoxetine did not.”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [10]
The scientific literature on protracted antidepressant withdrawal consists mainly of a few qualitative studies and case reports, with one small cohort study of three PWS cases.
“The scientific literature’s foundation of case reports documenting withdrawal syndrome thus far contains only a few studies qualitatively describing protracted withdrawal,19,20,35,36 and one small cohort study including three cases of PWS.37”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
PWS was ascertained using Chouinard and Chouinard diagnostic criteria: at least 6 months of continuous antidepressant use, with emergence of new and/or more intense symptoms after discontinuation that last beyond the initial 6 weeks of acute withdrawal.
“PWS was ascertained based on diagnostic criteria proposed by Chouinard and Chouinard, specifically ⩾6 months of continuous antidepressant use, with emergence of new and/or more intense symptoms after discontinuation that last beyond the initial 6 weeks of acute withdrawal.”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
The study included only reports where antidepressants were taken continuously for at least 6 months and withdrawal symptoms definitely persisted beyond 6 weeks.
“Therefore, we included only reports where antidepressants were taken continuously for at least 6 months and where withdrawal symptoms definitely persisted beyond 6 weeks.”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
The observation that reinstatement was rarely successful is consistent with Chouinard and Chouinard's view that protracted withdrawal does not seem very amenable to reinstatement or other conventional drug treatment.
“Nevertheless, this observation is consistent with Chouinard and Chouinard: protracted withdrawal does not seem very amenable to reinstatement or other conventional drug treatment.35”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
Long known in addiction medicine and from benzodiazepines, protracted withdrawal from antidepressants has been recognized only recently.
“Long known in addiction medicine and from benzodiazepines,20,31 protracted withdrawal from antidepressants has been recognized only recently.35”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
The narratives analyzed in this study indicate that consumers are able to distinguish drug withdrawal from the symptoms of the original illness, because withdrawal symptoms are experienced as more intense, urgent, and often unprecedented, that is, qualitatively different.
“The narratives analyzed in this study likewise indicate that consumers are able to distinguish drug withdrawal from the symptoms of the original illness, since withdrawal symptoms are experienced as more intense, urgent, and often unprecedented, that is, qualitatively different.28,30,35”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
The literature is largely silent about the treatment of protracted withdrawal syndrome (PWS) from antidepressants because PWS has been poorly recognized.
“As PWS from antidepressants has been so poorly recognized, the literature is largely silent about its treatment.35,39”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
Some of the diagnostic criteria proposed by Chouinard and Chouinard are not supported by robust scientific evidence due to a lack of research on PWS and hence are debatable, for example, the prerequisites of at least 6 months of continuous drug use and peak of symptom onset between 1 day and 6 weeks.
“Finally, some of the diagnostic criteria proposed by Chouinard and Chouinard are not supported by robust scientific evidence due to a lack of research on PWS and hence are debatable, for example, the prerequisites of at least 6 months of continuous drug use and peak of symptom onset between 1 day and 6 weeks.35”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
To minimize misattribution bias, we relied on the diagnostic criteria proposed by Chouinard and Chouinard, which require that symptoms are described as novel or more intense than ever experienced before.
“To minimize misattribution bias, we relied on the diagnostic criteria proposed by Chouinard and Chouinard,35 which require that symptoms are described as novel or more intense than ever experienced before.”
From Protracted withdrawal syndrome after stopping antidepressants: a descriptive quantitative analysis of consumer narratives from a large internet forum (2020) · cites this paper as [35]
Untreated withdrawal symptoms may be mild and resolve spontaneously in 1-3 weeks; in other cases they may persist for months or even years, leading to persistent post-withdrawal disorder.
“Untreated symptoms may be mild and resolve spontaneously in 1–3 weeks; in other cases they may persist for months or even years,40–45 leading to what has been defined as persistent post-withdrawal disorder.”
From May antidepressant drugs worsen the conditions they are supposed to treat? The clinical foundations of the oppositional model of tolerance (2020) · cites this paper as [41]
The clinical phenomena of antidepressant discontinuation pertain to withdrawal syndromes and do not differ from those that occur with other psychotropic drugs.
“However, this position is no longer tenable in view of current evidence that indicates that the clinical phenomena pertain to withdrawal syndromes and do not differ from those that occur with other psychotropic drugs.”
From May antidepressant drugs worsen the conditions they are supposed to treat? The clinical foundations of the oppositional model of tolerance (2020) · cites this paper as [41]
The withdrawal syndrome encompasses a broad range of somatic symptoms (e.g. headache, dizziness, flu-like symptoms, nausea).
“The withdrawal syndrome encompasses a broad range of somatic symptoms (e.g. headache, dizziness, flu-like symptoms, nausea).”
From May antidepressant drugs worsen the conditions they are supposed to treat? The clinical foundations of the oppositional model of tolerance (2020) · cites this paper as [41]
Withdrawal symptoms following discontinuation of antidepressant treatment have been described with any type of AD, but particularly with SSRI, venlafaxine, and duloxetine.
“They have been described with any type of AD, but particularly with SSRI, venlafaxine, and duloxetine.”
From May antidepressant drugs worsen the conditions they are supposed to treat? The clinical foundations of the oppositional model of tolerance (2020) · cites this paper as [41]
With both benzodiazepines and antidepressants, withdrawal reactions and post-withdrawal syndromes may ensue despite slow tapering.
“It would seem that, with both types of drugs, that withdrawal reactions and post-withdrawal syndromes may ensue, despite slow tapering.”
From May antidepressant drugs worsen the conditions they are supposed to treat? The clinical foundations of the oppositional model of tolerance (2020) · cites this paper as [41]
After their introduction, more pronounced problems occurred with most of the newer antidepressants.
“However, in due course after their introduction, more pronounced problems occurred with most of the newer antidepressants.40–46”
From May antidepressant drugs worsen the conditions they are supposed to treat? The clinical foundations of the oppositional model of tolerance (2020) · cites this paper as [41]
Benzodiazepines can cause paradoxical reactions such as agitation, excitement, insomnia, and talkativeness, especially in children and the elderly.
“Paradoxical reactions may also occur, such as increased agitation, excitement, insomnia, and talkativeness with benzodiazepines, particularly in children and the elderly [33].”
From Iatrogenic Factors in Psychopathology (2019) · cites this paper as [33]
Similar misclassification may apply to the limited effectiveness of novel antidepressants.
“Similar considerations may apply to the limited effectiveness of novel antidepressants [25].”
From The Deceptive Manifestations of Treatment Resistance in Depression: A New Look at the Problem (2020) · cites this paper as [25]
One consequence is the development of drugs geared to treatment resistance, such as ketamine/esketamine, which would not survive a classic RCT in depression.
“One is the development of drugs geared to treatment resistance, such as ketamine/esketamine [25], which would not survive the test of a classic RCT in depression.”
From The Deceptive Manifestations of Treatment Resistance in Depression: A New Look at the Problem (2020) · cites this paper as [25]
Cites
Boyer, E. W., & Shannon, M. (2005) · New England Journal of Medicine · doi:10.1056/nejmra041867 · Cited by 1,821 · see citing works
Signs and Symptoms of Tobacco Withdrawal
Hughes, J. R. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800030107013 · Cited by 1,669 · see citing works
A double‐blind, placebo‐controlled trial
Pinals, R. S., Kaplan, S. B., Lawson, J. G., & Hepburn, B. (1986) · Arthritis & Rheumatism · doi:10.1002/art.1780291202 · Cited by 1,355 · see citing works
Selective serotonin reuptake inhibitor discontinuation syndrome: a randomized clinical trial
Rosenbaum, J. F., Fava, M., Hoog, S. L., Ascroft, R. C., & Krebs, W. B. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00126-7 · Cited by 574 · see citing works
Management of Drug and Alcohol Withdrawal
Kosten, T. R., & O'Connor, P. G. (2003) · New England Journal of Medicine · doi:10.1056/nejmra020617 · Cited by 563 · see citing works
Fava, G. A., Gatti, A., Belaise, C., Guidi, J., & Offidani, E. (2015) · Psychotherapy and Psychosomatics · doi:10.1159/000370338 · Cited by 421 · see citing works
Withdrawal Reaction after Long-Term Therapeutic Use of Benzodiazepines
Busto, U., Sellers, E. M., Naranjo, C. A., Cappell, H., Sanchez-Craig, M., & Sykora, K. (1986) · New England Journal of Medicine · doi:10.1056/nejm198610023151403 · Cited by 369 · see citing works
Withdrawal reactions from chlordiazepoxide (?Librium?)
Hollister, L. E., Motzenbecker, F. P., & Degan, R. O. (1961) · Psychopharmacologia · doi:10.1007/bf00429621 · Cited by 340 · see citing works
Neuroleptic-induced supersensitivity psychosis: clinical and pharmacologic characteristics
(1980) · American Journal of Psychiatry · doi:10.1176/ajp.137.1.16 · Cited by 301 · see citing works
Self-citation(2004) · PubMed · Cited by 296 · see citing works
Management of Cocaine Abuse and Dependence
Mendelson, J. H., & Mello, N. K. (1996) · New England Journal of Medicine · doi:10.1056/nejm199604113341507 · Cited by 291 · see citing works
Antidepressant discontinuation reactions: Are preventable and simple to treat
Haddad, P., Lejoyeux, M., & Young, A. (1998) · BMJ · doi:10.1136/bmj.316.7138.1105 · Cited by 286 · see citing works
Serotonin syndrome: a brief review.
Birmes, P. J., Coppin, D., Schmitt, L., et al. (2003) · PubMed · Cited by 225 · see citing works
Neuroleptic-induced supersensitivity psychosis
(1978) · American Journal of Psychiatry · doi:10.1176/ajp.135.11.1409 · Cited by 224 · see citing works
Self-citationAntidepressant Discontinuation Syndromes: Clinical Relevance, Prevention and Management
Haddad, P. M. (2001) · Drug Safety · doi:10.2165/00002018-200124030-00003 · Cited by 214 · see citing works
Discontinuation Symptoms After Treatment With Serotonin Reuptake Inhibitors: A Literature Review
Zajecka, J., Tracy, K. A., & Mitchell, S. (1997) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v58n0702 · Cited by 209 · see citing works
Selective serotonin reuptake inhibitor discontinuation syndrome: proposed diagnostic criteria.
(2000) · PubMed Central · Cited by 207 · see citing works
Rebound Insomnia: A New Clinical Syndrome
Kales, A., Scharf, M. B., & Kales, J. D. (1978) · Science · doi:10.1126/science.684426 · Cited by 200 · see citing works
Five Weeks to Escape the Sleeping-pill Habit
Oswald, I., & Priest, R. G. (1965) · BMJ · doi:10.1136/bmj.2.5470.1093 · Cited by 182 · see citing works
Michelson, D., Fava, M., Amsterdam, J., Apter, J., Londborg, P., Tamura, R., & Tepner, R. G. (2000) · British Journal of Psychiatry · doi:10.1192/bjp.176.4.363 · Cited by 181 · see citing works
Rebound anxiety in anxious patients after abrupt withdrawal of benzodiazepine treatment
(1984) · American Journal of Psychiatry · doi:10.1176/ajp.141.7.848 · Cited by 176 · see citing works
Self-citationProtracted withdrawal syndromes from benzodiazepines
Ashton, H. (1991) · Journal of Substance Abuse Treatment · doi:10.1016/0740-5472(91)90023-4 · Cited by 170 · see citing works
Chouinard, G., & Chouinard, V.-A. (2008) · Psychotherapy and Psychosomatics · doi:10.1159/000112883 · Cited by 168 · see citing works
Self-citationLENGTH OF TREATMENT WITH ANXIOLYTIC SEDATIVES AND RESPONSE TO THEIR SUDDEN WITHDRAWAL
Covi, L., Lipman, R. S., Pattison, J. H., Derogatis, L. R., & Uhlenhuth, E. H. (1973) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1973.tb04398.x · Cited by 162 · see citing works
Antidepressant discontinuation syndromes
Haddad, P. M., Anderson, I. M., & Rosenbaum, J. F. (2004) · Oxford University Press eBooks · doi:10.1093/med/9780198527480.003.0010 · Cited by 160 · see citing works
Early Morning Insomnia with Rapidly Eliminated Benzodiazepines
Kales, A., Soldatos, C. R., Bixler, E. O., & Kales, J. D. (1983) · Science · doi:10.1126/science.6131538 · Cited by 138 · see citing works
Severe cases of neuroleptic-induced supersensitivity psychosis
Chouinard, G. (1991) · Schizophrenia Research · doi:10.1016/0920-9964(91)90050-2 · Cited by 123 · see citing works
Self-citationThe SSRI discontinuation syndrome
Haddad, P. M. (1998) · Journal of Psychopharmacology · doi:10.1177/026988119801200311 · Cited by 123 · see citing works
Nielsen, M., Hansen, E. H., & Gøtzsche, P. C. (2012) · Addiction · doi:10.1111/j.1360-0443.2011.03686.x · Cited by 103 · see citing works
Alcohol, barbiturate and benzodiazepine withdrawal syndromes: clinical management.
Sellers, E. M. (1988) · Europe PMC (PubMed Central) · Cited by 86 · see citing works
Fava, G. A., Bernardi, M., Tomba, E., & Rafanelli, C. (2007) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145706007462 · Cited by 80 · see citing works
Kales, A. (1970) · Archives of General Psychiatry · doi:10.1001/archpsyc.1970.01750030019004 · Cited by 68 · see citing works
Margolese, H. C., Chouinard, G., Beauclair, L., & Bélanger, M.-C. (2002) · Journal of Clinical Psychopharmacology · doi:10.1097/00004714-200208000-00003 · Cited by 61 · see citing works
Self-citationWhy is it so difficult to stop psychiatric drug treatment?
Moncrieff, J. (2006) · Medical Hypotheses · doi:10.1016/j.mehy.2006.03.009 · Cited by 59 · see citing works
A Canadian multicenter, double-blind study of paroxetine and fluoxetine in major depressive disorder
Chouinard, G., Saxena, B., Bélanger, M.-C., Ravindran, A., Bakish, D., Beauclair, L., Morris, P., Vasavan Nair, N. P., Manchanda, R., Reesal, R., et al. (1999) · Journal of Affective Disorders · doi:10.1016/s0165-0327(98)00188-8 · Cited by 57 · see citing works
Self-citationBelaise, C., Gatti, A., Chouinard, V.-A., & Chouinard, G. (2012) · Psychotherapy and Psychosomatics · doi:10.1159/000341178 · Cited by 45 · see citing works
Self-citationBelaise, C., Gatti, A., Chouinard, V.-A., & Chouinard, G. (2014) · Psychotherapy and Psychosomatics · doi:10.1159/000362317 · Cited by 44 · see citing works
Self-citation(2006) · PubMed · Cited by 33 · see citing works
Withdrawal symptoms after long-term treatment with low-potency neuroleptics.
Chouinard, G., Bradwejn, J., Annable, L., Jones, B. D. M., & Ross‐Chouinard, A. (1984) · PubMed · Cited by 23 · see citing works
Self-citationTreatment of supersensitivity psychosis with antiepileptic drugs: report of a series of 43 cases.
Chouinard, G., & Sultan, S. (1990) · PubMed · Cited by 21 · see citing works
Self-citationDiscontinuing Paroxetine: A Personal Account
Shoenberger, D. (2002) · Psychotherapy and Psychosomatics · doi:10.1159/000063650 · Cited by 12 · see citing works
A ten-year follow-up study of supersensitivity psychosis
Chouinard, G. (1990) · Biological Psychiatry · doi:10.1016/0006-3223(90)90231-p · Cited by 8 · see citing works
Self-citationFactors affecting the course of tardive dyskinesia: A ten year follow up study
Chouinard, G., Annable, L., Ross‐Chouinard, A., et al. (1989) · Biological Psychiatry · doi:10.1016/0006-3223(89)91817-9 · Cited by 5 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Carvalho, A. F., Sharma, M. S., Brunoni, A. R., Vieta, E., & Fava, G. A. (2016) · Psychotherapy and Psychosomatics · doi:10.1159/000447034 · Cited by 650 · see citing works
Malhi, G. S., Bell, E., Bassett, D., Boyce, P., Bryant, R., Hazell, P., Hopwood, M., Lyndon, B., Mulder, R., Porter, R., et al. (2021) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867420979353 · Cited by 614 · see citing works
Current Psychosomatic Practice
Fava, G. A., Cosci, F., & Sonino, N. (2017) · Psychotherapy and Psychosomatics · doi:10.1159/000448856 · Cited by 302 · see citing works
Antipsychotic-Induced Dopamine Supersensitivity Psychosis: Pharmacology, Criteria, and Therapy
Chouinard, G., Samaha, A.-N., Chouinard, V.-A., Peretti, C.-S., Kanahara, N., Takase, M., & Iyo, M. (2017) · Psychotherapy and Psychosomatics · doi:10.1159/000477313 · Cited by 270 · see citing works
Self-citationAcute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications
Cosci, F., & Chouinard, G. (2020) · Psychotherapy and Psychosomatics · doi:10.1159/000506868 · Cited by 265 · see citing works
Self-citationFava, G. A., Benasi, G., Lucente, M., Offidani, E., Cosci, F., & Guidi, J. (2018) · Psychotherapy and Psychosomatics · doi:10.1159/000491524 · Cited by 209 · see citing works
Methodological Recommendations for Trials of Psychological Interventions
Guidi, J., Brakemeier, E.-L., Bockting, C. L. H., Cosci, F., Cuijpers, P., Jarrett, R. B., Linden, M., Marks, I., Peretti, C. S., Rafanelli, C., et al. (2018) · Psychotherapy and Psychosomatics · doi:10.1159/000490574 · Cited by 205 · see citing works
Guidi, J., Tomba, E., & Fava, G. A. (2016) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2015.15040476 · Cited by 167 · see citing works
Guidi, J., & Fava, G. A. (2021) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2020.3650 · Cited by 155 · see citing works
Fava, G. A., & Guidi, J. (2020) · World Psychiatry · doi:10.1002/wps.20698 · Cited by 143 · see citing works
Bockting, C. L. H., Klein, N. S., Elgersma, H. J., van Rijsbergen, G. D., Slofstra, C., Ormel, J., Buskens, E., Dekker, J., de Jong, P. J., Nolen, W. A., et al. (2018) · The Lancet Psychiatry · doi:10.1016/s2215-0366(18)30100-7 · Cited by 130 · see citing works
Well-Being Therapy: Current Indications and Emerging Perspectives
Fava, G. A. (2016) · Psychotherapy and Psychosomatics · doi:10.1159/000444114 · Cited by 96 · see citing works
Fava, G. A., Cosci, F., Guidi, J., & Tomba, E. (2017) · Depression and Anxiety · doi:10.1002/da.22629 · Cited by 95 · see citing works
Fava, G. A., Guidi, J., Rafanelli, C., & Rickels, K. (2017) · Psychotherapy and Psychosomatics · doi:10.1159/000480038 · Cited by 93 · see citing works
Lerner, A., & Klein, M. (2019) · Brain Communications · doi:10.1093/braincomms/fcz025 · Cited by 89 · see citing works
Fava, G. A. (2020) · Therapeutic Advances in Psychopharmacology · doi:10.1177/2045125320970325 · Cited by 84 · see citing works
The clinical role of well-being therapy
Guidi, J., Rafanelli, C., & Fava, G. A. (2018) · Nordic Journal of Psychiatry · doi:10.1080/08039488.2018.1492013 · Cited by 85 · see citing works
Iatrogenic Factors in Psychopathology
Fava, G. A., & Rafanelli, C. (2019) · Psychotherapy and Psychosomatics · doi:10.1159/000500151 · Cited by 82 · see citing works
Benzodiazepines as a monotherapy in depressive disorders: a systematic review
Benasi, G., Guidi, J., Offidani, E., Balon, R., Rickels, K., & Fava, G. A. (2018) · Psychotherapy and Psychosomatics · doi:10.1159/000486696 · Cited by 79 · see citing works
Discontinuing Antidepressant Drugs: Lesson from a Failed Trial and Extensive Clinical Experience
Fava, G. A., & Belaise, C. (2018) · Psychotherapy and Psychosomatics · doi:10.1159/000492693 · Cited by 77 · see citing works
Hengartner, M. P., Schulthess, L., Sorensen, A., & Framer, A. (2020) · Therapeutic Advances in Psychopharmacology · doi:10.1177/2045125320980573 · Cited by 74 · see citing works
When Discontinuing SSRI Antidepressants Is a Challenge: Management Tips
Jha, M. K., Rush, A. J., & Trivedi, M. H. (2018) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2018.18060692 · Cited by 73 · see citing works
Hengartner, M. P. (2020) · Therapeutic Advances in Psychopharmacology · doi:10.1177/2045125320921694 · Cited by 72 · see citing works
Gueorguieva, R., Chekroud, A. M., & Krystal, J. H. (2017) · The Lancet Psychiatry · doi:10.1016/s2215-0366(17)30038-x · Cited by 67 · see citing works
Understanding and Managing Withdrawal Syndromes After Discontinuation of Antidepressant Drugs
Fava, G. A., & Cosci, F. (2019) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.19com12794 · Cited by 69 · see citing works
Cloos, J.-M., Bocquet, V., Rolland-Portal, I., Koch, P., & Chouinard, G. (2015) · Psychotherapy and Psychosomatics · doi:10.1159/000434755 · Cited by 57 · see citing works
Self-citationBehavioral Toxicity Revisited: Iatrogenic Comorbidity in Psychiatric Evaluation and Treatment
Fava, G. A., Cosci, F., Offidani, E., & Guidi, J. (2016) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0000000000000570 · Cited by 55 · see citing works
Effects of Treatment Discontinuation in Clinical Psychopharmacology
Baldessarini, R. J., & Tondo, L. (2019) · Psychotherapy and Psychosomatics · doi:10.1159/000497334 · Cited by 52 · see citing works
Clinical Pharmacopsychology: Conceptual Foundations and Emerging Tasks
Fava, G. A., Tomba, E., & Bech, P. (2017) · Psychotherapy and Psychosomatics · doi:10.1159/000458458 · Cited by 52 · see citing works
Antidepressant withdrawal – the tide is finally turning
Hengartner, M. P., Davies, J., & Read, J. (2020) · Epidemiology and Psychiatric Sciences · doi:10.1017/s2045796019000465 · Cited by 48 · see citing works
The Deceptive Manifestations of Treatment Resistance in Depression: A New Look at the Problem
Fava, G. A., Cosci, F., Guidi, J., & Rafanelli, C. (2020) · Psychotherapy and Psychosomatics · doi:10.1159/000507227 · Cited by 48 · see citing works
Groot, P. C., & van Os, J. (2020) · Therapeutic Advances in Psychopharmacology · doi:10.1177/2045125320932452 · Cited by 49 · see citing works
Chiappini, S., & Schifano, F. (2018) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0000000000000814 · Cited by 44 · see citing works
Is There a Potential of Misuse for Venlafaxine and Bupropion?
Schifano, F., & Chiappini, S. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00239 · Cited by 38 · see citing works
Récalt, A. M., & Cohen, D. (2019) · Psychotherapy and Psychosomatics · doi:10.1159/000496734 · Cited by 38 · see citing works
Scholten, W. D., Batelaan, N. M., van Oppen, P., Smit, J. H., Hoogendoorn, A. W., van Megen, H. J. G. M., Cath, D. C., & van Balkom, A. J. L. M. (2018) · Psychotherapy and Psychosomatics · doi:10.1159/000489498 · Cited by 33 · see citing works
Cohen, D., & Recalt, A. (2019) · Psychotherapy and Psychosomatics · doi:10.1159/000496733 · Cited by 28 · see citing works
Clinical Methodology Matters in Epidemiology: Not All Benzodiazepines Are the Same
Cosci, F., Guidi, J., Balon, R., & Fava, G. A. (2015) · Psychotherapy and Psychosomatics · doi:10.1159/000437201 · Cited by 27 · see citing works
The hidden costs of financial conflicts of interest in medicine
Fava, G. A. (2016) · Psychotherapy and Psychosomatics · doi:10.1159/000442694 · Cited by 25 · see citing works
Outcomes of hyperbolic tapering of antidepressants
van Os, J., & Groot, P. C. (2023) · Therapeutic Advances in Psychopharmacology · doi:10.1177/20451253231171518 · Cited by 22 · see citing works
Failure to Respond after Reinstatement of Antidepressant Medication: A Systematic Review
Bosman, R. C., Waumans, R. C., Jacobs, G. E., Oude Voshaar, R. C., Muntingh, A. D. T., Batelaan, N. M., & van Balkom, A. J. L. M. (2018) · Psychotherapy and Psychosomatics · doi:10.1159/000491550 · Cited by 21 · see citing works
Shapiro, B. B. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4995-4 · Cited by 20 · see citing works
Scholten, W., Batelaan, N., & Van Balkom, A. (2020) · Therapeutic Advances in Psychopharmacology · doi:10.1177/2045125320933404 · Cited by 17 · see citing works
Eserian, J. K., Blanco, V. P., Mercuri, L. P., Matos, J. D. R., & Galduróz, J. C. F. (2023) · Psychiatry Research · doi:10.1016/j.psychres.2023.115537 · Cited by 15 · see citing works
What psychologists need to know about psychotropic medications
Tomba, E., Guidi, J., & Fava, G. A. (2018) · Clinical Psychology & Psychotherapy · doi:10.1002/cpp.2154 · Cited by 11 · see citing works
Cosci, F., Chouinard, V.-A., & Chouinard, G. (2024) · Psychotherapy and Psychosomatics · doi:10.1159/000540031 · Cited by 11 · see citing works
Self-citationFalse Beliefs in Academic Psychiatry: The Case of Antidepressant Drugs
Hengartner, M. P., & Plöderl, M. (2018) · Ethical Human Psychology and Psychiatry · doi:10.1891/1559-4343.20.1.6 · Cited by 10 · see citing works
Patacchini, A., & Cosci, F. (2020) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0000000000001154 · Cited by 10 · see citing works
Rennwald, A., & Hengartner, M. P. (2025) · Epidemiology and Psychiatric Sciences · doi:10.1017/s204579602500023x · Cited by 8 · see citing works
“PAWS includes new symptoms as well as original symptoms but with increased intensity, appearing days or weeks, sometimes even months, after treatment discontinuation and lasting from over a month to years (Chouinard and Chouinard, 2015; Hengartner et al. , 2020; Lerner and Klein, 2019).”
InfluentialCosci, F. (2017) · Personalized Medicine in Psychiatry · doi:10.1016/j.pmip.2016.11.001 · Cited by 8 · see citing works
- Authors
- Chouinard, G., & Chouinard, V.-A.
- Affiliations
- McGill University (CA)
- Harvard University (US)
- Venue
- Psychotherapy and Psychosomatics
- Publisher
- S. Karger AG
- Published
- 2015
- Volume
- 84
- Issue
- 2
- Pages
- 63-71
- ISSN
- 0033-3190 (ISSN-L)
- 1423-0348
- OpenAlex
- W2084924129
- Cited by
- 164
- References
- 44
- Citations by year
- 2026: 4 · 2025: 9 · 2024: 16 · 2023: 11 · 2022: 12 · 2021: 20 · 2020: 21 · 2019: 22 · 2018: 18 · 2017: 14 · 2016: 10 · 2015: 6
- FWCI
- 11.53
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Psychotherapy and Psychosomatics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Health Sciences › Medicine › Psychiatry and Mental health › Electroconvulsive Therapy Studies
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Pharmacovigilance and Adverse Drug Reactions
- Keywords
- selective serotonin reuptake inhibitors, relapse and recurrence, serotonin-norepinephrine reuptake inhibitors, benzodiazepine withdrawal, elimination half-life, antidepressant tapering, antidepressant withdrawal syndrome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-11.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-11.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review