Doxepin

mixture of cis- and trans-isomers

Systematic (IUPAC) name
(E/Z)-3-(dibenzo[b,e]oxepin-11(6H)-ylidene)-N,N-dimethylpropan-1-amine
Clinical data
Trade names	Sinequan, Zonalon
AHFS/Drugs.com	monograph
MedlinePlus	a682390
Pregnancy cat.	C (AU) Not recommended. Animal studies have shown embryotoxic properties.
Legal status	℞ Prescription only
Routes	Oral, IM, IV
Pharmacokinetic data
Bioavailability	Absolute: 25% When main metabolite desmethyldoxepin is included: 31%
Metabolism	Hepatic
Half-life	Doxepin 17 hours, main metabolite Desmethyldoxepin 51 hours
Excretion	Renal
Identifiers
CAS number	1668-19-5 Y
ATC code	N06AA12
PubChem	CID 3158
IUPHAR ligand	1225
DrugBank	DB01142
ChemSpider	3046 Y
UNII	5ASJ6HUZ7D Y
KEGG	D07875 Y
ChEBI	CHEBI:4710 Y
ChEMBL	CHEMBL101740 N
Chemical data
Formula	C19H21NO
Mol. mass	279.376 g/mol
SMILES CN(C)CC/C=C1C2=C(C=CC=C2)OCC3=C/1C=CC=C3
InChI InChI=1S/C19H21NO/c1-20(2)13-7-11-17-16-9-4-3-8-15(16)14-21-19-12-6-5-10-18(17)19/h3-6,8-12H,7,13-14H2,1-2H3 Y Key:ODQWQRRAPPTVAG-UHFFFAOYSA-N Y
N (what is this?)  (verify)

Doxepin (Sinequan) is a psychotropic agent with tricyclic antidepressant and anxiolytic properties, known under many brand-names such as Aponal, the original preparation by Boehringer-Mannheim, now part of the Roche group; Adapine, Doxal (Orion), Deptran, Sinquan and Sinequan (Pfizer). As doxepin hydrochloride, it is the active ingredient in cream-based preparations (Zonalon and Xepin) for the treatment of dermatological itch. Doxepin is also used for the treatment of sleep maintenance, and the tradename of doxepin for this indication is Silenor.

Medical uses

Doxepin is used to treat depression, anxiety disorders, and as a second line treatment of chronic idiopathic urticaria (hives).

• Insomnia
• low dose doxepin (3 to 6 mg) is an FDA approved use in the treatment of insomnia
• Helps with oral mucositis following radiation therapy for head and neck cancer

Pregnancy and lactation

If doxepin is used chronically during pregnancy, the newborn may show a withdrawal syndrome with agitation, impaired cardio-respiratory functions, disturbed urination and defecation.^{[citation needed]} Caution should be exerted in treating pregnant women on a regular basis.^{[citation needed]}

Doxepin is found in significant amounts in the milk of lactating women.^{[citation needed]} If therapy is necessary, breastfeeding should be interrupted during treatment. In order to maintain supply, the mother may pump and discard the milk during her treatment.^{[citation needed]}

Contraindications

Absolute

• known hypersensitivity to doxepin or other dibenzazepines or other ingredients of the drug^{[citation needed]}
• acute intoxication with alcohol, sedatives, analgesics and other psychoactive drugs^{[citation needed]}
• acute delirium tremens^{[citation needed]}
• untreated closed angle glaucoma^{[citation needed]}
• hypertrophy of the prostate with urine retention^{[citation needed]}
• paralytic ileus^{[citation needed]}

Relative

• hypertrophy of the prostate without urine retention^{[citation needed]}
• reduced function of the bone marrow^{[citation needed]}
• organic brain disorders^{[citation needed]}
• increased risk of seizures, preexisting epilepsy^{[citation needed]}
• preexisting cardiac damage, particular some arrhythmias (e.g. sinoatrial blockage)^{[citation needed]}

Caution

• other forms of preexisting cardiac damage (other arrhythmias, insufficience)^{[citation needed]}
• MAOIs of the irreversible type (tranylcypromine among others) : These drugs should normally be stopped at least 2 weeks before therapy with doxepin is started.^{[citation needed]}

Children under 12 years of age should not be treated, because no sufficient clinical experience exists for this group of age.^{[citation needed]}

Tricyclic antidepressant drugs, particularly when given in high doses, can induce sinus tachycardia, changes in conduction time, and arrhythmias. A few instances of unexpected death have been reported in patients with cardiovascular disorders.^{[citation needed]} Myocardial infarction and stroke have also been reported with drugs of this class. Therefore, doxepin should be administered with extreme caution to patients with a history of cardiovascular disease, those with circulatory lability, and elderly patients. In such cases, treatment should be initiated with low doses with progressive increases only if required and tolerated, and the patients should be under close surveillance at all dosage levels.^{[citation needed]}

Since tricyclic agents are known to reduce the seizure threshold, doxepin should be used with caution in patients with a history of convulsive disorders.^{[citation needed]} Concurrent administration of ECT and doxepin may be hazardous and, therefore, such treatment should be limited to patients for whom it is essential.

Close supervision is required when doxepin is given to hyperthyroid patients or those receiving thyroid medication because of the possibility of cardiovascular toxicity.^{[citation needed]} At doses above 150 mg/day, it may block the antihypertensive effect of guanethidine and related compounds.

Before initiation of treatment a complete and differentiated blood count should be taken.^{[citation needed]} If any value is pathologic, the blood count should be monitored closely under therapy with doxepin. If values are normal, blood counts should be taken during therapy in regular intervals (recommended: weekly during first month of therapy, monthly during the next 2 months, every 3 months afterwards).

Liver-function studies should be performed periodically.

Side effects

• Central Nervous System: fatigue, dizziness, drowsiness, lightheadedness, confusion, nightmares, agitation, increased anxiety, insomnia, seizures (infrequently), delirium, rarely induction of hypomania and schizophrenia (stop medication immediately), extrapyramidal side-effects (rarely), abuse in patients with polytoxikomania (rarely), tinnitus^{[citation needed]}
• Anticholinergic: dry mouth, constipation, even ileus (rarely), difficulties in urinating, sweating, precepitation of glaucoma^{[citation needed]}
• Antiadrenergic: hypotension, postural collapse (if patient arises too fast from lying/sitting position to standing), arrhythmias (sinus-tachycardia, bradycardia, av-blockade)^{[citation needed]}
• Allergic/toxic: skin rash, photosensitivity, liver damage of the cholostatic type (rarely), hepatitis (extremely rare), leuko- or thrombopenia (rarely), agranulocytosis (very rarely), hypoplastic anemia (rarely)^{[citation needed]}
• Others: frequently increased appetite, weight gain, rarely nausea, frequently impaired sexual function in men (impotence, ejaculation-difficulties), rarely hypertension, rarely polyneuropathy, in both sexes breast-enlargement and galactorrhea (rarely).^{[citation needed]}
• May increase or decrease liver function in some patients.

Suicidal patients

Patients with suicidal thoughts, or those with previous suicidal attempts, should be monitored closely under treatment with Doxepin. Perhaps, the decision is made to hospitalize high-risk patients until remission. At least, the smallest amount of Doxepin should be prescribed at one time to minimize the risk of deliberate overdose.^{[citation needed]}

Drug abuse and dependence

Doxepin has an extremely low potential for abuse and psychological dependence (mostly noted with multiple-substance abusers, possibly due to the strong anxiolytic action of Doxepin).^{[citation needed]}

Withdrawal symptoms frequently seen when treatment with doxepin is stopped abruptly (agitation, anxiety, insomnia, sometimes activation of mania or rebound depression) can be avoided by reducing the daily dose of Doxepin gradually by approximately 25% each week. If treatment has to be stopped at once due to medical reasons, the use of a benzodiazepine (e.g. Lorazepam, Clonazepam, or Alprazolam) for a maximum of 4 weeks as needed will usually suppress withdrawal symptoms.^{[citation needed]}

Other remarks

Doxepin may worsen psychotic conditions like schizophrenia and should be given with caution. The antipsychotic treatment should be continued.^{[citation needed]}

With Zonalon and Xepin; in most countries an external form (cream) is available for the treatment of itching skin disease; the effect is probably due to the affinity of doxepin for H1 and H2 receptors and action on muscarinic receptors. Doxepin is the most anxiolytic of all the tricyclic antidepressants.^{[citation needed]}

Interactions

• Irreversible MAOIs: agitation, delirium, coma, hyperpyrexia (high fever), seizures and severe changes in blood pressure. potentially fatal. Treatment-resistant hospitalized patients may be treated concomitantly with an MAO-inhibitor, if they are closely monitored by an expert and the initial dose of both drugs is low.^{[citation needed]}
• Increased drug actions:^{[citation needed]}
  • other antidepressants, barbiturates, narcotics, sedating antihistaminics, anticonvulsive drugs, alcohol - resulting in increased central depression
  • anticholinergics (antiparkinsonian agents, tri- and tetracyclic antidepressants) - resulting in increased anticholinergic action (dry mouth, obstipation etc.)^{[citation needed]}
  • Cimetidine: impairs the excretion of Doxepin - increased central depression and anticholinergic effects
  • Sympathomimetics (also those used in local anesthetics like Noradrenaline): sympathomimetic effects increased (increased blood pressure, pulse rate, paleness of skin etc.)^{[citation needed]}
  • Nitrates and Antihypertensives (e.g. Beta-Blockers) - increased antihypertensive action with pronounced fall in blood pressure
• Decreased drug actions:
  • Guanethidine, Reserpine, Guanfacine: antihypertensive effects decreased^{[citation needed]}
  • Clonidine: antihypertensive effects decreased and risk of (massive) rebound hypertension.^{[citation needed]}

Overdose

Main article: Tricyclic antidepressant overdose

If overdose is suspected, local poison control centers or emergency departments can provide advice. United States residents can call the US national poison hotline at 1-800-222-1222. Other worldwide poison centers can be found at the World directory of poisons centers.

The symptoms and the treatment of an overdose are largely the same as for the other tricyclic antidepressants.

Pharmacology

Doxepin inhibits the reuptake of serotonin and norepinephrine.^{[citation needed]} Its actions of the reuptake of dopamine are negligible.^{[citation needed]} Doxepin also has antagonistic effects at a variety of receptors:

• Extremely strong: H₁, H₂ (K_i = 0.7 nM)^{[citation needed]}
• Strong: 5-HT₂, α₁-adrenergic, mACh^{[citation needed]}
• Moderate: 5-HT₁, local anesthetic action.^{[citation needed]}

History

Doxepin was synthesized by Stach and Spingler from the German drug manufacturer C. F. Boehringer & Söhne GmbH in Mannheim. It was tested from 1963 to 1968 in different German and Swiss psychiatric institutions and was approved in Germany and elsewhere thereafter. The antidepressive effects were found to be excellent. Strong anxiolytic and sedative properties were also demonstrated. Doxepin has been in clinical use for several decades. The drug plays an important role in many indications today, not only in psychiatry/neurology.^{[citation needed]}

See also

• Tricyclic antidepressant