Arch Gen Psychiatry. Specifically, the risk for seizures may be increased. Monitor therapy, Mianserin: May enhance the anticholinergic effect of Anticholinergic Agents. Specifically, serotonergic agents may enhance dopamine blockade, possibly increasing the risk for neuroleptic malignant syndrome. Management: Avoid concomitant use of tapentadol and benzodiazepines or other CNS depressants when possible. Monitor therapy, Antipsychotic Agents (Second Generation [Atypical]): Blood Pressure Lowering Agents may enhance the hypotensive effect of Antipsychotic Agents (Second Generation [Atypical]). Monitor therapy, Trimeprazine: May enhance the CNS depressant effect of CNS Depressants. ALWAYS consult with your doctor or pharmacist. Adv Pharmacol. The site is secure. These agents should only be combined if alternative treatment options are inadequate. Symptoms arising may vary with antidepressant however commonly include nausea, vomiting, diarrhea, headaches, light-headedness, dizziness, diminished appetite, sweating, chills, tremors, paresthesias, fatigue, somnolence, and sleep disturbances (eg, vivid dreams, insomnia). Use our structured and evidence-based datasets to unlock new insights and accelerate drug research. 2021 Sep 23;12:717999. doi: 10.3389/fpsyt.2021.717999. Serum sodium in at-risk populations (as clinically indicated) (De Picker 2014); pulse rate and blood pressure prior to and during therapy; ECG/cardiac status in older adults and patients with cardiac disease; suicidal ideation (especially at the beginning of therapy, after initiation, or when doses are increased or decreased); signs/symptoms of serotonin syndrome; hepatic transaminases (periodically during therapy in patients with preexisting hepatic impairment). Am J Psychiatry. FLUoxetine may increase the serum concentration of Tricyclic Antidepressants. May be used to treat obsessive-compulsive disorder and disorders with an obsessive-compulsive component (e.g. Monitor therapy, Amifostine: Blood Pressure Lowering Agents may enhance the hypotensive effect of Amifostine. Clomipramine, a tricyclic antidepressant, is the 3-chloro derivative of Imipramine. Management: Monitor for signs and symptoms of serotonin syndrome/serotonin toxicity (eg, hyperreflexia, clonus, hyperthermia, diaphoresis, tremor, autonomic instability, mental status changes when these agents are combined. ~ 17 L/kg (range: 9-25 L/kg). Patent 3,515,785; June 2,1970; assigned to Geigy Chemical Corp. Drug created at June 13, 2005 13:24 / Updated at June 08, 2023 10:20, Structured drug data for data science & ML, Clinical intelligence tool for your software, Search for drug interactions with our API, Get drug allergy and cross sensitivities info. Use of suvorexant with alcohol is not recommended, and the use of suvorexant with any other drug to treat insomnia is not recommended. Depression like thoughts of suicide, anxiety, emotional instability, or confusion. Data from randomized, double-blind studies supports the use of clomipramine in the treatment of major depressive disorder DUAG 1986, DUAG 1990, DUAG 1999, Lpine 2000, Zohar 2003. Clomipramine is rapidly absorbed from the gastrointestinal tract and demethylated in the liver to its primary active metabolite, desmethylclomipramine. -, Greist JH, Jefferson JW, Kobak KA, Katzelnick DJ, Serlin RC. Monitor therapy, Molsidomine: May enhance the hypotensive effect of Blood Pressure Lowering Agents. Seizures: May cause seizures (relationship to dose and/or duration of therapy); do not exceed maximum doses. Based on the Canadian Psychiatric Association guidelines for the management of anxiety disorders, TCAs like clomipramine are second-line choices for panic disorder. In nonelective procedures, consider use of prophylactic anticonvulsants. Panic disorder (off-label use): Oral: Initial: 10 to 25 mg daily; increase by 10 to 25 mg every 2 to 3 days based on efficacy and tolerability to a target dose of 50 to 150 mg/day, in 1 to 3 divided doses; guidelines recommend doses ranging from 50 to 250 mg/day (APA [Stein 2009]; Caillard 1999; Lecrubier 1997a; Lecrubier 1997b; WFSBP [Bandelow 2012]). One death involved a patient suspected of ingesting a dose of 7000 mg. Consider therapy modification, Ergot Derivatives: May enhance the serotonergic effect of Serotonergic Agents (High Risk). Management: Monitor for signs and symptoms of serotonin syndrome/serotonin toxicity (eg, hyperreflexia, clonus, hyperthermia, diaphoresis, tremor, autonomic instability, mental status changes) when these agents are combined. TCAs also block histamine-H1 receptors, 1-adrenergic receptors and muscarinic receptors, which accounts for their sedative, hypotensive and anticholinergic effects (e.g. Compared with placebo, antidepressants increase the risk of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. This could result in serotonin syndrome. Management: Avoid concomitant use of opioid agonists and benzodiazepines or other CNS depressants when possible. [, Borkowska A, Pilaczynska E, Araszkiewicz A, Rybakowski J: [The effect of sertraline on cognitive functions in patients with obsessive-compulsive disorder]. In a scientific statement from the American Heart Association, clomipramine has been determined to be an agent that may exacerbate underlying myocardial dysfunction (magnitude: moderate) (AHA [Page 2016]). If a severe, acute reaction such as DRESS occurs, discontinue clomipramine immediately. [, Schrickx JA, Fink-Gremmels J: Inhibition of P-glycoprotein by psychotherapeutic drugs in a canine cell model. Monitor therapy, Alizapride: May enhance the CNS depressant effect of CNS Depressants. This could result in serotonin syndrome. PMC Consider therapy modification, Prostacyclin Analogues: May enhance the hypotensive effect of Blood Pressure Lowering Agents. 1998 Nov;140(1):120-2. St John's Wort may decrease the serum concentration of Serotonergic Agents (High Risk). However, antidepressants have. Monitor therapy, Dronedarone: Tricyclic Antidepressants may enhance the arrhythmogenic effect of Dronedarone. [. Some combinations may be specifically contraindicated. Management: Monitor for signs and symptoms of serotonin syndrome/serotonin toxicity (eg, hyperreflexia, clonus, hyperthermia, diaphoresis, tremor, autonomic instability, mental status changes) and increased TCA concentrations/effects if these agents are combined. Management: Avoid concurrent use of abiraterone with CYP2D6 substrates that have a narrow therapeutic index whenever possible. PMC Talk with the doctor. Arch Gen Psychiatry. Exceptions: Apraclonidine; Brimonidine (Ophthalmic); Lofexidine. This could result in serotonin syndrome. Avoid combination, Droperidol: May enhance the CNS depressant effect of CNS Depressants. Monitor therapy, Methotrimeprazine: CNS Depressants may enhance the CNS depressant effect of Methotrimeprazine. Enrollment should be done as early in pregnancy as possible. Epub 2004 Mar 1. Do not use dapoxetine within 14 days of monoamine oxidase inhibitor use. Amphetamines may enhance the serotonergic effect of Tricyclic Antidepressants. Sexual dysfunction: Has been associated with a high incidence of male sexual dysfunction. Consider therapy modification, HydrOXYzine: May enhance the CNS depressant effect of CNS Depressants. Anafranil (clomipramine hydrochloride) Capsules USP is an antiobsessional drug that belongs to the class (dibenzazepine) of pharmacologic agents known as tricyclic antidepressants. Avoid combination, Cinacalcet: May increase the serum concentration of Tricyclic Antidepressants. The presence of this polymorphism in CYP2C19 is associated with reduced or poor metabolism of clomipramine. It is used to treat obsessive-compulsive problems. Specifically, the risk of gastrointestinal adverse effects may be increased. Elimination half-lives of clomipramine and desmethylclomipramine are approximately 32 hours (range: 19-37 hours) and 69 hours (range: 54-77 hours), respectively, after a 150-mg oral dose. Adrenal tumor: Use with caution in patients with tumors of the adrenal medulla (eg, pheochromocytoma, neuroblastoma); may cause hypertensive crises. APA and NICE guidelines suggest tapering therapy over at least several weeks with consideration to the half-life of the antidepressant; antidepressants with a shorter half-life may need to be tapered more conservatively. No such dose change is recommended for women. Management: When amifostine is used at chemotherapy doses, blood pressure lowering medications should be withheld for 24 hours prior to amifostine administration. It was thought that tricyclic antidepressants work exclusively by inhibiting the re-uptake of the neurotransmitters norepinephrine and serotonin by nerve cells. Clomipramine may decrease the hypoglycemic activities of Acarbose. QuiNIDine may increase the serum concentration of Tricyclic Antidepressants. Management: Consider alternatives to this drug combination. [, Gillman PK: Tricyclic antidepressant pharmacology and therapeutic drug interactions updated. Pregnant women exposed to antidepressants during pregnancy are encouraged to enroll in the National Pregnancy Registry for Antidepressants (NPRAD). The patient's family or caregiver should be alerted to monitor patients for the emergence of suicidality and associated behaviors such as anxiety, agitation, panic attacks, insomnia, irritability, hostility, impulsivity, akathisia, hypomania, and mania; patients should be instructed to notify their health care provider if any of these symptoms or worsening depression or psychosis occur. 3-(3-chloro-10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethyl-1-propanamine, 3-(3-chloro-5H-dibenzo[b,F]azepin-5-yl)-N,N-dimethylpropan-1-amine. Serum concentrations were not found to correlate to withdrawal symptoms (ter Horst 2012). For the treatment of depression and depression accompanied by anxiety, agitation or sleep disturbance Build, train, & validate predictive machine-learning models with structured datasets. Low sodium like headache, difficulty focusing, trouble with memory, confusion, weakness, seizures, or change in balance. The https:// ensures that you are connecting to the Monitor therapy, Dronabinol: May enhance the CNS depressant effect of CNS Depressants. This activity will highlight the mechanism of action . Management: Monitor for signs and symptoms of serotonin syndrome/serotonin toxicity (eg, hyperreflexia, clonus, hyperthermia, diaphoresis, tremor, autonomic instability, mental status changes) if these agents are combined. J Vet Pharmacol Ther. Their primary mechanism of action is the modulation of neurotransmission and the consequent accumulation of monoamines, such as serotonin and noradrenaline. Lorcaserin may increase the serum concentration of Tricyclic Antidepressants. Clomipramine is a tricyclic antidepressant used in the treatment of obsessive-compulsive disorder and disorders with an obsessive-compulsive component, such as depression, schizophrenia, and Tourettes disorder. and transmitted securely. Peak plasma concentrations occurred 2-6 hours following oral administration of a single 50 mg dose. Avoid combination, OxyCODONE: CNS Depressants may enhance the CNS depressant effect of OxyCODONE. Clomipramine is a tricyclic antidepressant used in the therapy of obsessive-compulsive disorder. Management: Monitor for signs and symptoms of serotonin syndrome/serotonin toxicity (eg, hyperreflexia, clonus, hyperthermia, diaphoresis, tremor, autonomic instability, mental status changes) when these agents are combined. 2001 Dec;11(66):472-5. Monitor therapy, Tetrahydrocannabinol and Cannabidiol: May enhance the CNS depressant effect of CNS Depressants. Management: Do not use serotonergic agents (high risk) with dapoxetine or within 7 days of serotonergic agent discontinuation. This could result in serotonin syndrome. Monitor therapy, Almotriptan: May enhance the serotonergic effect of Serotonergic Agents (High Risk). Toxicity Clomipramine can be fatal in overdose. Premature ejaculation (PE) is perhaps the most common sexual dysfunction amongst men. Monitor therapy, Cocaine (Topical): May enhance the adverse/toxic effect of Tricyclic Antidepressants. Clomipramine and metabolites excreted in urine and in feces (via biliary elimination). 1996 Jun;277(3):1659-64. Monitor therapy, Thyroid Products: May enhance the arrhythmogenic effect of Tricyclic Antidepressants. Mechanism of action Clomipramine is a strong, but not completely selective serotonin reuptake inhibitor (SRI), as the active main metabolite desmethyclomipramine acts preferably as an inhibitor of noradrenaline reuptake. Consider therapy modification, Acetylcholinesterase Inhibitors: May diminish the therapeutic effect of Anticholinergic Agents. Monitor therapy, Amantadine: May enhance the anticholinergic effect of Anticholinergic Agents. Source: Wolters Kluwer Health. Consider therapy modification, Citalopram: Tricyclic Antidepressants may enhance the serotonergic effect of Citalopram. Management: Patients on drugs with substantial anticholinergic effects should avoid using any solid oral dosage form of potassium chloride. Discontinue treatment (and any concomitant serotonergic agent) immediately if signs/symptoms arise. Critical manifestations of overdose include cardiac dysrhythmias, severe hypotension, convulsions, and CNS depression including coma. Monitor therapy, CYP2D6 Inhibitors (Strong): May decrease the metabolism of CYP2D6 Substrates (High risk with Inhibitors). Monitor therapy, Perampanel: May enhance the CNS depressant effect of CNS Depressants. 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