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Encyclopedia > Clomipramine

Clomipramine chemical structure
Clomipramine Image File history File links Clomipramine. ...

 ?
IUPAC name
CAS number
303-49-1
ATC code
N06AA04
PubChem
2801
DrugBank
APRD00253
Chemical formula C9H23ClN2
Molecular weight 314.9
Bioavailability Oral ~50%
Metabolism Hepatic
Elimination half-life Clomipramine ~35 hours
Desmethylclomipramine (main active metabolite) ~50 hours
Excretion Renal
Pregnancy category Unknown.
May cause withdrawal symptoms in newborn.
Legal status Rx Only, not scheduled
Routes of administration Oral, I.M., I.V.

Clomipramine (brand-name Anafranil®) is a tricyclic antidepressant. IUPAC nomenclature is a system of naming chemical compounds and of describing the science of chemistry in general. ... CAS registry numbers are unique numerical identifiers for chemical compounds, polymers, biological sequences and alloys. ... The Anatomical Therapeutic Chemical Classification System is used for the classification of drugs. ... A section of the Anatomical Therapeutic Chemical Classification System. ... PubChem is a database of chemical molecules . ... DrugBank is a database available at the University of Alberta that provides information about thousands of products. ... A chemical formula (also called molecular formula) is a concise way of expressing information about the atoms that constitute a particular chemical compound. ... The molecular mass of a substance (less accurately called molecular weight and abbreviated as MW) is the mass of one molecule of that substance, relative to the unified atomic mass unit u (equal to 1/12 the mass of one atom of carbon-12). ... In pharmacology, bioavailability is used to describe the fraction of an administered dose of medication that reaches the systemic circulation, one of the principal pharmacokinetic properties of drugs. ... Santorio Santorio (1561-1636) in his steelyard balance, from Ars de statica medecina, first published 1614 Metabolism (from μεταβολισμος (metabolismos)) is the biochemical modification of chemical compounds in living organisms anggjgjhnd cell (b). ... The liver is an organ in vertebrates including humans. ... The elimination half-life of a drug (or any xenobiotic agent) refers to the timecourse necessary for the quantity of the xenobiotic agent in the body (or plasma concentration) to be reduced to half of its original level through various elimination processes. ... Excretion is the biological process by which an organism chemically separates waste products from its body. ... Kidneys viewed from behind with spine removed The kidneys are bean-shaped excretory organs in vertebrates. ... The pregnancy category of a pharmaceutical agent is an assessment of the risk of fetal injury due to the pharmaceutical, if it is used as directed by the mother. ... The regulation of therapeutic goods, that is drugs and therapeutic devices, varies by jurisdiction. ... Chemical structure of the tricyclic antidepressant amitriptyline Tricyclic antidepressants are a class of antidepressant drugs first used in the 1950s. ...

Contents


Indications

  • Depression with lack of energy or mild agitation
  • Obsessive Compulsive Disorders (OCD)
  • Panic attacks with or without Agoraphobia
  • Narcolepsy
  • chronic pain with or without organic disease, particular headache of the tension type
  • Enuresis (involuntary nightly urinating in sleep) in children / adolescents
  • Off label, sometimes antidepressants of this type have been found helpful in reducing relapses in cocaine addicts and to help repair cocaine-caused neurotransmitter imbalances and early brain damage. Further studies are needed for Clomipramine in this regard.

It may take 2 to 3 weeks before the full effects of this medication are noticed in all indications. Clinical depression is a state of sadness or melancholia that has advanced to the point of being disruptive to an individuals social functioning and/or activities of daily living. ... For other things named OCD, see OCD (disambiguation). ... A panic attack is a period of intense fear or discomfort, typically with an abrupt onset and usually lasting no more than 30 minutes. ... This article is in need of attention from an expert on the subject. ... Narcolepsy is a neurological condition characterized by severe fatigue, irresistible episodes of sleep and general sleep disorder. ... Chronic pain was originally defined as pain that has lasted 6 months or longer. ...


Contraindications

  • Concomitant therapy with an (irreversible) MAO-Inhibitor (e.g. Tranylcypromin, Phenelzin)
  • Acute intoxication with central depressants (alcohol, psychoactive drugs, narcotics)
  • States of confusion (caution), absolutely contraindicated in patients with coma and Delirium tremens
  • Patients with massive agitation or anxiety (give sedative drugs concomittantly)
  • Hypersensitivity/Allergy against Clomipramine or other related tricyclic compounds
  • Hypertrophy of the Prostate with urine retention (=difficulty in urinating)
  • Caution : Hypertrophy of the Prostate without urine retention
  • Preexisting closed angle glaucoma
  • Epilepsy and other conditions which lower the seizure-threshold (alcohol-withdrawal, active brain tumors)
  • Serious liver disease (elimination is decreased), if Clomipramine is given consider dose reduction
  • Serious kidney disease (elimination is decresed), if Clomipramine is given consider dose reduction
  • Severe hypotension, shock, serious cardiovascular dysfunction (postinfarctous states, heart insufficience, arrhythmias), avoid high oral doses or injections/infusions
  • Preexisting bone marrow depression (leukopenia, thrombopenia, anemia, pancytopenia), can be worsened by Clomipramine
  • Overfunction of the thyreoid gland makes the patient more sensitive to side-effects of Clomipramine. Cautious doses should be used and the overfunction should be treated.
  • Caution should be exerted when treating pediatric patients under 18 yrs. of age

Pharmacology

Clomipramine is the 3-chloro derivative of Imipramine. Clomipramine is a strong, but not completely selective Serotonic-Reuptake-Inhibitor (SRI), as the active main metabolite Desmethyclomipramine acts preferably as inhibitor of Noradrenaline-Reuptake. Other hydroxy-metabolites are also active. Alpha-1-Receptor blockage and beta-down-regulation as well as postsynaptic antagonism on H1 (histaminergic)-receptors have been noted. A blockade of Sodium-channels and NDMA-receptors might, as with other tricyclics, account for its effect in chronic pain, particular of the neuropathic type.


Clomipramine might as well show stimulating effects as well as mild sedating ones. Anyway, strongly agitated patients initially need combination therapy with a benzodiazepine or with Chlorprothixene. Clomipramine shows excellent activity in any indication, but has the disadvantage of a higher incidence of seizures than seen with other tricyclic antidepressants (up to a dose of 250mg daily in 0,5%, more than 300 mg in 2%). Chlorprothixene is a typical antipsychotic drug of the thioxanthine class. ...


Due to its action against anxiety disorders and panic attacks it is the only drug with 2 entries in the 'Essential Drugs' list of the WHO.


Regarding compulsive disorders it is now the 'gold standard' of therapy, against which other drugs are measured.


Interesting results indicate that the antidepressant activity correlates with the plasma-level of the main active metabolite Desmethylclomipramine, while antidepressant activity merely correlates with the plasma-level of Clomipramine in unchanged form.


Veterinary uses

Clomipramine is widely used for the treatment of disturbed behaviour of dogs, cats, and horses.


History

Clomipramine was developed in the 1960's by the Swiss drug manufacturer Geigy and has been in clinical use worldwide for decades.


Side effects

Clomipramine is not harmless and may have a broad range of side-effects:

  • Central Nervous System: Often, fatigue, dizziness, lightheadedness, headaches, confusion, agitation, insomnia, nightmares, increased anxiety, seizures (0,5% to 2%, see above), rarely hypomania or induction of schizophrenia (immediate termination of therapy required), and extrapyramidal side-effects (pseudoparkinsonism, dyskinesia, rarely tardive dyskinesia) are noted.
  • Anticholinergic side-effects in different grades of severity are quite common: dry mouth, constipation, rarely ileus (paralysis of the large intestine, life-threatening), difficulties in urinating, sweating, precipation of glaucoma (may lead to permanent eye-damage or even blindness, if untreated). The incidence of dental caries may be increased due to dry mouth. Careful mouth hygiene should be instituted. Visit your dentist regularly for professional prophylaxis.
  • Antiadrenergic side-effects occur very frequently due to strong central and peripheral blockage of alpha-receptors: hypotension, postural collapse (when patient is rising too fast from lying or sitting position to standing), arrhythmias (sinus-tachycardia, bradycardia, av-block, rarely other forms of cardiac problems). Preexisting heart insufficience can be worsened.

Most of these side-effects are dose related and/or tolerance will develop with continued use. It has been suggested that Primary insomnia be merged into this article or section. ... This article is about the medical condition. ... Hypomania is a state involving combinations of: elevated mood, irritability, racing thoughts, people-seeking, hypersexuality, grandiose thinking, religiosity, and pressured speech. ... In human anatomy, the extrapyramidal system is a neural network located in the brain that is part of the motor system involved in the coordination of movement. ... Dyskinesia is a medical condition meaning the person afflicted makes bad or abnormal movements. ... Tardive dyskinesia is a serious neurological disorder caused by the long-term and/or high-dose use of dopamine antagonists, usually antipsychotics and among them especially the typical antipsychotics. ... Intestinal obstruction can be partial or complete blockage of the intestine, either large or small. ... Caries is a progressive destruction of any kind of bone structure, including the skull, the ribs and other bones. ... In physiology and medicine, hypotension refers to an abnormally low blood pressure. ... Bradycardia, as applied in adult medicine, is defined as a heart rate of under 60 beats per minute, though it is seldom symptomatic until the rate drops below 50 beat/min [1]. It is also less commonly known as brachycardia. ...

  • Allergic/toxic: skin reactions and photosensitivity with increased frequency of sunburns are seen in a few percentage of cases. Avoid prolonged sun exposure. Wear a sunscreen and protective clothing. Rarely liver damage of the cholostatic type, hepatitis, and leukopenia or other forms of blood dyskrasia are seen, also severe acute allergy including difficulties in breathing, skin reaction, chest pain etc. Call a doctor immediately.
  • Other side effects may include heartburn, weight gain, but also nausea and bruxism - teeth-grinding while asleep - (the latter due to the stong inhibition of reuptake of serotonin).
  • The drug often causes sexual problems in men (e.g. impotence, ejaculation difficulties). In about 5% of patients, it can instead cause inadvertent orgasms when yawning (see "Yin, Yang and Yawn" - Snopes article on Clomipramine)

Hepatitis is a gastroenterological disease, featuring inflammation of the liver. ... Leukopenia or leukocytopenia refers to a decrease in the number of circulating white blood cells (leukocytes) in the blood. ... Bruxism (derived from Greek βρυγμός, male noun - grinding [teeth]) is grinding of the teeth. ... Serotonin (5-hydroxytryptamine, or 5-HT) is a monoamine neurotransmitter synthesised in serotonergic neurons in the central nervous system and enterochromaffin cells in the gastrointestinal tract. ...

Drug Abuse and Dependence

Clomipramine has no known potential for abuse and dependence. It is not a controlled substance.


Withdrawal symptoms occurring when Clomipramine is stopped abruptly (agitation, fatigue, nausea, headaches, insomnia, sometimes activation of mania and rebound of depression or anxiety) is not indicative of dependence and can be avoided, if Clomipramine is gradually withdrawn by reducing the daily dose by approximately 25% weekly. If medical reasons dictate an immediate termination of treatment, a short-term course of benzodiazepines (up to 4 weeks as needed) will usually suppress the unpleasant withdrawal symptoms.


Suicidal Patients

Depression itself can lead to thoughts or attempts of suicide. Tell your doctor immediately if you have any suicidal thoughts, or other mental/mood changes. Keep all medical appointments so your doctor can monitor your progress closely. Emotionally unstable patients or those with suicidal thoughts shought receive the smallest amount of the drug feasible. Often cotreatment with a sedative drug (e.g. a benzodiazepine or chlorprothixene) is necessary until remission of depression is evident. Chlorprothixene is a typical antipsychotic drug of the thioxanthine class. ...


Other Reasons for Caution

Caution is advised when using this drug in the elderly, because they may be more sensitive to the effects of the drug (e.g., confusion may occur or worsen).


This drug should be used during pregnancy only if clearly needed. Discuss the risks and benefits with your doctor.


This drug is excreted into breast milk. The effects on the infant are not known at this time. Consult your doctor before breast-feeding.


Drug Interactions

Clomipramine shows a number of clinical significant interactions, either due to central depressant or stimulant activity of the other drug or due to interference of the other drug with the metabolization and elimination of Clomipramine or vice versa. Some examples are:

  • MAO inhibitors (e.g., furazolidone, linezolid, phenelzine, selegiline, tranylcypromine) : Severe reactions including central excitation, hypertensive crises, bizarre behaviour, psychosis, seizures, coma and death are possible.
  • Central Stimulants : Potentially dangerous central excitation with agitation and anxiety may be encountered.
  • SSRI type antidepressants (eg. Fluoxetine) : Side effects of Clomipramine are increased.
  • Drugs with central depressant activity (tranquilizers, alcohol, narcotics) : Increased central depression (dizziness, drowsiness etc.) is frequently noted.
  • antihypertenive drugs : The risk of hypotension, collapse, and tachycardia is increased.

Do not start or stop any drug (also OTC-medications against cold, sleeping aids with Diphenhydramine or Doxylamine, St. John's Wort etc.) without your physician's approval. Monoamine oxidase inhibitors (MAOIs) are a class of antidepressant drugs prescribed for the treatment of depression. ... Furazolidone (also marketed as Furoxone) is an antibiotic used to treat diarrhea and enteritis caused by bacteria or protozoan infections. ... Linezolid is a synthetic systemic antibiotic drug. ... Phenelzine (brand name Nardil) is an antidepressant drug that belongs to the monoamine oxidase inhibitor (MAOI) class of drugs. ... Selegiline (l-deprenyl, Eldepryl® or Anipryl® [veterinary]) is a drug used for the treatment of early-stage Parkinsons disease and senile dementia. ... Tranylcypromine is an antidepressant drug. ... SSRI is an acronym that stands for several things: It is a class of antidepressants called selective serotonin reuptake inhibitor SSRI also is used as the stock symbol for Silver Standard Resources Inc. ...


Dosage and Proper Usage

Start with small doses (2 or 3 times 25mg daily or 75mg in slow released form, as directed by your doctor). The dose is increased in regular intervals by your prescribing physician (the usual dose per day is 100-225mg). Doses up to 300mg may be used, but these are associated with an increased risk of seizures. This medication may be taken with food to prevent stomach upset.


In hospitalized patients initial i.m.-injections and very slow i.v.-infusions can be used, but the risk of hypotension and seizures may be increased with parental drug use. The advantage is that the onset of action may be faster.


Usually, Clomipramine needs some weeks to reach its maximum effects and needs to be given as longterm treatment, sometimes for life (narcolepsy). Sometimes, in patients with narcolepsy the full effect of Clomipramine is not sufficient. In these cases terminate treatment with Clomipramine gradually and try a commonly used central stimulant (e.g. Modafinil, Methylphenidate, Methamphetamine).


Clomipramine is not able to increase the mood of non-depressive persons and that any unindicated use may be dangerous.


Overdose

If overdose is suspected, contact your local poison control center or emergency room immediately. US residents can call the US national poison hotline at 1-800-222-1222.


Canadian residents should call their local poison control center directly.


Ten out of 12 patients presenting with manifest clomipramine overdose survived with appropriate treatment. These 10 patients took clomipramine doses of up to 5 grams. The 2 patients who died ingested 5.75 and 7 grams, respectively. Outside the US one patient died who took only 0.75 grams. Lethal doses may be lower, if other drugs have been taken in an overdose, too, particular central nervous depressants.


Symptoms of overdose may include flushing, fast or irregular heartbeat, dry mouth, drowsiness, confusion, agitation, enlarged pupils, seizures, and loss of consciousness. Therapy is largely symptomatic. Inducing emesis, gastric lavage, and giving activated charcoal can all be tried when an oral overdose is detected early. If anticholiergic side-effects (dry mouth, obstipation, urine retention) dominate the poisoning, Physostigmine can be given repeatedly in small doses, but Physostigmine may increase the risk of seizures. Seizures can be treated with slow i.v.-injections of Diazepam (5 to 10mg) until they subside. Barbiturates should be avoided, as they can deepening respiratory depression and may lead to postictal coma. Lidocain can be used to treat cardiac arrhythmias. Correction of water and electrolyt-bilance and artificial breathing may be necessary. Continued monitoring of vital functions in an intensive care unit is also necessary.


Brands

  • Anafranil® registered TM of Novartis, sold worldwide
  • generics


Novartis International AG is a multinational pharmaceutical company based in Basel, Switzerland. ...

Antidepressants (ATC N06A) edit
Monoamine oxidase inhibitors: {Harmaline} {Nialamide} {Selegiline} {Isocarboxazid} {Iproniazid} {Iproclozide} {Moclobemide} {Phenelzine} {Toloxatone} {Tranylcypromine}

Dopamine reuptake inhibitors: {Bupropion} {Amineptine} An antidepressant is a medication designed to treat or alleviate the symptoms of clinical depression. ... A section of the Anatomical Therapeutic Chemical Classification System. ... Monoamine oxidase inhibitors (MAOIs) are a class of antidepressant drugs prescribed for the treatment of depression. ... Harmala, also known at various times as Telepathine and Banisterine, is a blanket term for a group of naturally occurring beta-carbolines including harmine, harmaline, and others. ... Nialamide (Espril®, Niamid®, Niaquitil®, Nuredal®, Nyazin®, and Psicodisten®) was one of the first MAOI (monoamine oxidase inhibitor) antidepressants. ... Selegiline (l-deprenyl, Eldepryl® or Anipryl® [veterinary]) is a drug used for the treatment of early-stage Parkinsons disease and senile dementia. ... Isocarboxazid is a nonselective hydrazine-derived monoamine oxidase inhibitor used in treatment resistant depression. ... Iproniazid is a monamine oxidase inhibitor (MAOI) that was developed as the first anti-depressant (Also first psychiatric drug). ... Moclobemide (sold as Aurorix®, Manerix®) is a psychiatric drug primarily used to treat depression and social anxiety. ... Phenelzine (brand name Nardil) is an antidepressant drug that belongs to the monoamine oxidase inhibitor (MAOI) class of drugs. ... Tranylcypromine is an antidepressant drug. ... Dopamine Reuptake Inhibitors or Dopamine Uptake Inhibitors are compounds that inhibit the reuptake of the neurotransmitter dopamine after it is released and used at the synapse. ... Bupropion (amfebutamone) (brand names Wellbutrin and Zyban) is an antidepressant of the aminoketone class, chemically unrelated to tricyclics or selective serotonin reuptake inhibitors (SSRIs). ... Amineptine is an atypical tricyclic antidepressant that selectively inhibits the reuptake of dopamine and to a lesser extent norepinephrine, thus exerting a powerful and fast-acting antidepressant effect. ...


Norepinephrine reuptake inhibitors: {Atomoxetine} {Reboxetine} {Viloxazine} {Maprotiline} Norepinephrine reuptake inhibitors (NRIs) are compounds that increase amounts of the neurotransmitter norepinephrine in the brain by inhibiting its reuptake at synapses. ... Atomoxetine is a drug used in the treatment of attention-deficit hyperactivity disorder (ADHD). ... Reboxetine is an antidepressant drug used in the treatment of clinical depression, panic disorder and ADD/ADHD. Its mesilate ( methanesulfonate) salt is sold under tradenames including Edronax®, Norebox®, Prolift®, Solvex® or Vestra®. Reboxetine has two chiral centers, but it only exists as two enantiomers, (R,R)-(-)- and (S,S)-(+)-reboxetine. ... Viloxazine is a bicyclic antidepressants[2] that inhibits the reuptake of serotonin, and to a lesser extent, dopamine and norepinephrine. ... To meet Wikipedias quality standards, this article may require cleanup. ...


Serotonin-norepinephrine reuptake inhibitors: {Desipramine} {Duloxetine} {Milnacipran} {Nefazodone} {Venlafaxine} Serotonin norepinephrine reuptake inhibitors (SNRIs) are a class of antidepressant used in the treatment of clinical depression and other affective disorders. ... Desipramine is a tricyclic antidepressant (TCA) that inhibits the reuptake of norepinephrine. ... Duloxetine hydrochloride (brand names: Cymbalta/Yentreve) is a medically used drug that primarily targets major depressive disorders (MDD), pain related to diabetic peripheral neuropathy and stress urinary incontinence (SUI). ... Milnacipran is an antidepressant of the serotonin-norepinephrine reuptake inhibitor class. ... // Introduction Serzone (nefazodone) Serzone ( Nefazodone HCl ) is an antidepressant drug formerly marketed by Bristol-Myers Squibb. ... Venlafaxine hydrochloride is a synthetic derivative of phenethylamine and a prescription antidepressant first introduced by Wyeth in 1993, and marketed under the trade names Effexor® for tablets and Effexor XR® for extended-release capsules. ...


Selective serotonin reuptake inhibitors: {Alaproclate} {Etoperidone} {Citalopram} {Escitalopram} {Fluoxetine} {Fluvoxamine} {Paroxetine} {Sertraline} {Zimelidine} Selective serotonin reuptake inhibitors (SSRIs) are a class of antidepressants for treating depression, anxiety disorders and some personality disorders. ... Citalopram or nitalapram is an antidepressant drug used to treat the depression associated with mood disorders. ... Escitalopram is a medication developed by the Danish pharmaceutical company Lundbeck, that acts as a selective serotonin reuptake inhibitor or SSRI. It is typically used as an antidepressant to treat depression associated with mood disorders although also may be used in the treatment of body dysmorphic disorder and anxiety. ... Fluoxetine hydrochloride is an antidepressant drug used medically in the treatment of depression, obsessive-compulsive disorder, bulimia nervosa, premenstrual dysphoric disorder and panic disorder. ... Fluvoxamine maleate (sold under the brand-names Luvox® and Faverin®) is a selective serotonin reuptake inhibitor. ... Paroxetine or paroxetine hydrochloride (sold as Paxil® in the United States and Canada; Seroxat® in Austria, the UK and China; Aropax® in Australia, New Zealand and Brazil; Pondera® in Brazil; Deroxat® in Switzerland and France, and Cebrilin in Latin America) is a selective serotonin reuptake inhibitor (SSRI) antidepressant. ... Sertraline hydrochloride (Zoloft®, Lustral®, Apo-Sertral®, Asentra®, Gladem®, Serlift®, Stimuloton®, Xydep®, Serlain®) is an orally administered antidepressant of the selective serotonin reuptake inhibitor (SSRI) type. ... // General Remars and History Zimelidine is a pyridylallylamine and has a structure different from other antidepressants. ...


Selective serotonin reuptake enhancers: {Tianeptine} Tianeptine (INN) (Stablon®, Coaxil®, Tatinol®), is structurally similar to the tricyclic antidepressants. ... Tianeptine (INN) (Stablon®, Coaxil®), is structurally similar to the tricyclic antidepressants. ...


Tricyclic antidepressants: {Amitriptyline} {Clomipramine} {Desipramine} {Dothiepin} {Doxepin} {Imipramine} {Lofepramine} {Nortriptyline} {Protriptyline} {Trimipramine} {Iprindole} {Opipramol} Chemical structure of the tricyclic antidepressant amitriptyline Tricyclic antidepressants are a class of antidepressant drugs first used in the 1950s. ... Amitriptyline hydrochloride is an antidepressant drug from the tricyclic antidepressant group, which is sold under the trade names Elavil®, Tryptanol® or Endep®. It is a white, odorless, crystalline compound which is freely soluble in water. ... Desipramine is a tricyclic antidepressant (TCA) that inhibits the reuptake of norepinephrine. ... dothiepin hydrochloride ... Doxepin is a tricyclic antidepressant, known under many brand-names such as Aponal®, the original preparation by Boehringer-Ingelheim, now part of the Roche group; Adapine®, Sinquan® and Sinequan® (Pfizer Inc. ... Imipramine (tradenames: Janimine®, Tofranil®) is an antidepressant medication belonging to a class called tricyclic antidepressants of the dibenzazepine group, mainly used in the treatment of clinical depression and enuresis. ... Nortriptyline is a tricyclic antidepressant marketed under the tradenames Aventyl® and Pamelor®. It is used to treat depression. ... Trimipramine is an tricyclic antidepressant with sedative and anxiolytic properties. ...


Tetracyclic antidepressants: {Maprotiline} {Mianserin} {Mirtazapine} {Amoxapine} The structure of the tetracyclic antidepressant mirtazapine A tetracyclic antidepressant is an antidepressant drug from the tetracyclic drug group. ... To meet Wikipedias quality standards, this article may require cleanup. ... Mirtazapine is a prescription antidepressant introduced by Organon International in 1996. ... Amoxapine (Asendin®; Asendis®; Defanyl®; Demolox®; Moxadil®) is a tricyclic antidepressant of the dibenzoxazepine class. ...


  Results from FactBites:
 
Clomipramine - Wikipedia, the free encyclopedia (1587 words)
Clomipramine is widely used for the treatment of disturbed behaviour of dogs, cats, and horses.
Clomipramine shows a number of clinical significant interactions, either due to central depressant or stimulant activity of the other drug or due to interference of the other drug with the metabolization and elimination of Clomipramine or vice versa.
Clomipramine is not able to increase the mood of non-depressive persons and that any unindicated use may be dangerous.
  More results at FactBites »


 
 

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