This dosage information may not include all the information needed to use Desipramine safely and effectively. See additional information for Desipramine.
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Usual Adult Dose for:
Usual Geriatric Dose for:
Usual Pediatric Dose for:
Additional dosage information:
Usual Adult Dose for Depression
The initial dose is 75 mg per day orally given as a single dose or in divided doses.
Maintenance dose: 100 to 200 mg per day.
May be further increased gradually to 300 mg per day if necessary.
Usual Geriatric Dose for Depression
The initial dose is 10 to 25 mg per day orally given as a single dose or in divided doses. The dose should be gradually increased according to tolerance and clinical response. The maximum dose is 150 mg per day.
Usual Pediatric Dose for Depression
The safety and efficacy of desipramine in children <13 years has not been established. However, the use of desipramine may be appropriate in some situations.
>= 6 years to 12 years:
10 to 30 mg per day or 1 to 5 mg/kg/day in divided doses.
Maximum dose is 5 mg/kg/day.
>= 13 years to 18 years:
The initial dose is 25 to 50 mg per day. The dose should be gradually increased to 100 mg per day given as a single dose or in divided doses. The maximum dose is 150 mg per day.
Renal Dose Adjustments
There are no data on dose adjustments in patients with renal dysfunction. However, caution is advised especially in cases of severe renal dysfunction.
Liver Dose Adjustments
There are no data on dose adjustments in patients with liver dysfunction. However, since desipramine is highly metabolized by the liver, caution is recommended especially in cases of severe liver dysfunction.
Lower dosages are recommended for outpatients compared to hospitalized patients, who are closely supervised. Following remission, maintenance medication may be required for a period of time and should be at the lowest dose that will maintain remission.
Maintenance therapy may be given on a once-daily schedule for patient convenience and compliance.
Treatment of patients requiring as much as 300 mg should generally be initiated in hospitals, where regular visits by the physician, skilled nursing care, and frequent electrocardiograms (EKGs) are available.
The concomitant administration of monoamine oxidase inhibitors and tricyclic antidepressants is considered contraindicated.
Children, adolescents, and young adults (18 to 24 years of age) with major depressive disorder and other psychiatric disorders may be at an increased risk of suicidal thinking and suicidality with antidepressant use, particularly during the first few months of treatment. Medical evidence has not shown this increased risk to exist in adults older than 24 years of age, but adults 65 years of age and older taking antidepressants appear to have a decreased risk of suicidality. The results of a meta-analysis indicate an overall favorable risk-to-benefit profile for the use of antidepressants (i.e., selective serotonin and/or norepinephrine reuptake inhibitors) in the treatment of pediatric patients (less than 19- years- old) with major depressive disorders (MDD), obsessive-compulsive disorder (OCD), or non- OCD anxiety disorders. Although this study also reports an overall increased risk of suicidal ideation/suicide attempt associated with the use of antidepressants in pediatric patients, the risk may be less than originally estimated. Additional prospective studies are warranted in order to confirm these findings.
Worsening of depression and/or increased suicidal thinking or behavior may always be a possibility in patients treated with antidepressant medications, particularly those being treated for depression. Anxiety, agitation, panic attacks, insomnia, irritability, hostility, impulsivity, akathisia (severe restlessness), hypomania, and mania have been reported in patients being treated with antidepressants for major depressive disorder as well as for other indications, both psychiatric and nonpsychiatric. It is unknown if these symptoms are a precursor to either worsening of depression or the emergence of suicidal impulses; however, there is concern that patients who experience one or more of these symptoms may be at increased risk for worsening depression or suicidality. Although the FDA has not concluded that antidepressant drugs cause worsening depression or suicidality, health care providers should be aware that worsening of symptoms could be due to the underlying disease or might be a result of drug therapy.
Health care providers should carefully monitor patients receiving antidepressants for possible and/or persistent worsening of depression or emergent suicidality, especially at the beginning of therapy or when the dose either increases or decreases. If symptoms are severe, abrupt in onset, or were not part of the patient's presenting symptoms, the health care provider will need to determine what intervention, including discontinuing or modifying the current drug therapy, is indicated. Prescriptions should be written for small quantities of drug to reduce the risk of an attempt to overdose. Health care providers should instruct patients, their families and their caregivers to be alert for the emergence of agitation, irritability, and the other symptoms described above, as well as the emergence of suicidality and worsening depression, and to report such symptoms immediately to their health care provider.
Because antidepressants are believed to have the potential for inducing manic episodes in patients with bipolar disorder, there is a concern about using antidepressants alone in this population. Therefore, patients should be adequately screened to determine if they are at risk for bipolar disorder before initiating antidepressant treatment so that they can be appropriately monitored during treatment. Such screening should include a detailed psychiatric history, including a family history of suicide, bipolar disorder, and depression.
No adjustment recommended
Dosages above 300 mg per day are not recommended. Maintenance therapy may be given on a once-daily schedule for patient convenience and compliance.