Citalopram
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Citalopram or nitalapram is an antidepressant drug used to treat depression associated with mood disorders. It is also used on occasion in the treatment of body dysmorphic disorder and anxiety.
Citalopram belongs to a class of drugs known as selective serotonin reuptake inhibitors (SSRIs). It is sold under the brand-names Celexa™ (U.S., Forest Laboratories, Inc.), Cipramil™ (Europe and Australia).
Citalopram was originally created by the pharmaceutical company Lundbeck although the patent for it expired in 2003, allowing other companies to legally produce generic versions.
Lundbeck has recently released a new SSRI drug called escitalopram oxalate (also known as Cipralex™ or Lexapro™) derived from the citalopram molecule.
Indications
Approved
Citalopram is primarily used to treat the symptoms of depression but can also be prescribed for panic disorder.Unapproved/Off-label/Investigational
Citalopram has been found to significantly reduce the symptoms of diabetic neuropathy and premature ejaculation.
There is also evidence that citalopram may be effective in the treatment of post-stroke pathological crying.
Side effects
Citalopram is safe and well tolerated in the therapeutic dose range of 20 to 60 mg/day. Distinct from some other agents in its class, Citalopram exhibits linear pharmacokinetics and minimal drug interaction potential, making it a better choice for the elderly, or comorbid patients.[link]Citalopram can have a number of adverse effects. In clinical trials, over 10% of patients reported fatigue, drowsiness, dry mouth, increased sweating (Hyperhidrosis), trembling, headache and/or dizziness, sleep disturbances, arrythmia, blood pressure and ejaculatory problems. In rare cases (around over 1% of cases), some allergic reactions, convulsions, mood changes, anxiety and confusion have been reported. Occasionally, panic attacks, thoughts of suicide or self-harm may occur or increase in the first few weeks, before the antidepressant effect starts.[link]
Citalopram is contraindicated in individuals taking MAOIs. It is considered relatively safe in overdose, although fatal cases of dosages 840 mg to 1960 mg have been reported.[link]
Stereochemistry
Citalopram has a chiral carbon atom, to which a 4-fluorophenyl group and an N,N-dimethyl-3-aminopropyl group are bonded. This stereocentre leads to the existence of two enantiomers of citalopram. They are termed S-(+)-citalopram and R-(−)-citalopram.
| S-(+)-citalopram | R-(−)-citalopram |
Citalopram is sold as a racemic mixture, consisting of 50% R-(−)-citalopram and 50% S-(+)-citalopram. Only the S-(+) enantiomer has the desired antidepressant effect. Lundbeck now markets the pure S-(+) enantiomer, the generic name of which is escitalopram. Escitalopram is sold as the oxalate - that is, the nitrogen atoms of the tertiary amine functional groups of two S-(+)-citalopram molecules are protonated by oxalic acid to form two escitalopram ammonium cations and an oxalate anion.
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External links
Pharmacological information and treatment study information:- http://www.biopsychiatry.com/citalopram.html
- [Celexa / Citalopram Fact Sheet]
- [FDA patient fact sheet on Citalopram hydrobromide]
- http://www.cipramil.com
- http://www.celexa.com
- [Celexa product page on Forest Laboratories web site]
- [Cipramil Patient Information Leaflet] Cipramil Patient Information Leaflet
References
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