Trimipramine
{{DrugProjectFormSinglePage |authorTag=Pratik Bahekar, MBBS [1] |genericName=Trimipramine |aOrAn=a |drugClass=Tricyclic antidepressant |indication=depression |hasBlackBoxWarning=Yes |adverseReactions=hypotension, tachycardia, constipation, xerostomia, dizziness, somnolence, blurred vision |blackBoxWarningTitle=TITLE |blackBoxWarningBody=Condition Name: (Content)
|fdaLIADAdult=
Depression
- 75 mg PO (divided into 1-3 doses per day), increase gradually to 150 mg/day to maximum 200 mg/day for outpatient treatment. Maintenance 50-150 mg/day PO, bedtime, for 3 months.
- 100 mg PO (divided into 1-3 doses per day), increase gradually to 200 mg/day, if unsatisfactory response in in 2-3 weeks, increase to a maximum 300 mg/day for inpatient treatment.
|offLabelAdultGuideSupport=Condition 1
- Developed by: (Organization)
- Class of Recommendation: (Class) (Link)
- Strength of Evidence: (Category A/B/C) (Link)
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|offLabelAdultNoGuideSupport=:* There is limited information about Off-Label Non–Guideline-Supported Use of Trimipramine in adult patients.
|fdaLIADPed=
Depression
- FDA approved for adolescents, and not for children.
- 50 mg/day PO may increase up to 100 mg/day for adolescents;
|offLabelPedGuideSupport=Condition 1
- Developed by: (Organization)
- Class of Recommendation: (Class) (Link)
- Strength of Evidence: (Category A/B/C) (Link)
- Dosing Information/Recommendation
- (Dosage)
|offLabelPedNoGuideSupport=:* There is limited information about Off-Label Non–Guideline-Supported Use of Trimipramine in pediatric patients. |contraindications=* Condition 1
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|warnings=Conidition 1
(Description) |clinicalTrials=Central Nervous System
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|postmarketing=Central Nervous System
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Cardiovascular
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Respiratory
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Gastrointestinal
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Hypersensitive Reactions
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Miscellaneous
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|fdaPatientInfo=For patient information about Trimipramine from NLM, click [[Trimipramine (patient information) |alcohol=Alcohol-Trimipramine interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication. }}