Chemical structure of clarithromycin.
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Biaxin

Clarithromycin is a macrolide antibiotic used to treat pharyngitis, tonsillitis, acute maxillary sinusitis, acute bacterial exacerbation of chronic bronchitis, pneumonia (especially atypical pneumonias associated with Chlamydia pneumoniae or TWAR), skin and skin structure infections, and, in HIV and AIDS patients to prevent, and to treat, disseminated Mycobacterium avium complex or MAC. more...

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In addition, it is sometimes used to treat Legionellosis.

Clarithromycin is available under several brandnames, for example Biaxin and Klacid.

History

Abbott Laboratories brought out clarithromycin in 1991.

Available forms

Clarithromycin is commonly administered in tablets (Biaxin®), extended-release tablets (Biaxin XL®), or oral suspension.

Mechanism of action

Clarithromycin prevents bacteria from growing, by interfering with their protein synthesis. Clarithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Clarithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain gram-negative bacteria, particularly Legionella pneumophilae. Besides this bacteriostatic effect, clarithromycin also has bactericidal effect on certain strains such as Haemophilus influenzae, Streptococcus pneumoniae and Neisseria gonorrhoeae.

Pharmacokinetics

Unlike erythromycin, clarithromycin is acid-stable and can therefore be taken orally without being protected from gastric acids. It is readily absorbed, and diffused into most tissues and phagocytes. Due to the high concentration in phagocytes, clarithromycin is actively transported to the site of infection. During active phagocytosis, large concentrations of clarithromycin is released. The concentration of clarithromycin in the tissues can be over 10 times higher than in plasma. Highest concentrations were found in liver and lung tissue.

Metabolism

Clarithromycin has a fairly rapid first-pass hepatic metabolism, i.e it is metabolised by the liver. However, this metabolite, 14-hydroxy clarithromycin is almost twice as active as clarithromycin. The half-life of clarithromycin is about 5 hours and 14-hydroxy clarithromycin's about 7 hours. Clarithromycin's and its metabolites' main routes of elimination are urinary and biliary excretion.

Side effects

Most common side-effects are gastrointestinal; diarrhea, nausea, abdominal pain and vomiting. Less common side-effects include headaches, rashes, alteration in senses of smell and taste.

Special Precautions

Allergic reactions can occur with clarithromycin use. People with a history of allergy, asthma, hay fever or hives seem to be more susceptible to these reactions. The reaction can be immediate and severe.

Allergic symptoms include wheezing, hives, itching, swelling, spasms in the throat and breathing tubes, joint and muscle pain, difficulty breathing, fever and skin rashes. Nausea and vomiting are not symptoms of an allergic reaction.

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Eszopiclone for treatment of transient and chronic insomnia
From American Family Physician, 6/15/05 by Andrea M. Wessell

Synopsis

Eszopiclone (Lunesta), a nonbenzodiazepine hypnotic agent, is indicated for the treatment of transient and chronic insomnia. Its mechanism of action is related to its activity at [gamma]-amino-butyric acid receptors. (1) Eszopiclone is an isomer of the hypnotic zopiclone (Imovane), which has been available in countries outside the United States for almost 20 years. (2)

Safety

The duration of action of eszopiclone is approximately eight hours, similar to zolpidem (Ambien) and longer than zaleplon (Sonata). The drug is metabolized in the liver by the CYP450 3A4 system, and dose adjustment is warranted in patients taking enzyme inhibitors such as ketoconazole (Nizoral). Eszopiclone is a Schedule IV con-trolled substance. No evidence of tolerance or dependence has been reported. (3,4) One case of nonfatal overdose with 36 mg of eszopiclone was reported in clinical trials. Rare cases of fatal overdose with zopiclone and concomitant central nervous system (CNS) depressants have been reported in European post-marketing studies. (1) Eszopiclone is pregnancy category C (animal studies only) and it is not approved for use in children.

Tolerability

Unpleasant taste (34 versus 3 percent), headache (17 versus 13 percent), and dizziness (7 versus 4 percent) were reported more commonly in patients taking eszopiclone than those taking placebo, respectively, in clinical trials. (1) Additive side effects are expected with concomitant use of substances with CNS-depressant activity, including alcohol. (1)

Effectiveness

There has been little published research on the effectiveness of eszopiclone in patients who have difficulty sleeping. One study (3) analyzed the use of eszopiclone for six months in 791 adult patients with chronic insomnia (age = 21 to 69 years; 63 per-cent were women). Patients reported results once weekly through an interactive voice response system and completed monthly study visits for safety and compliance assessments. After one week of therapy, eszopiclone-treated patients fell asleep a mean of 37 minutes faster, had 0.6 fewer nighttime awakenings, and slept 50 minutes longer than placebo-treated patients. Sleep quality, next-day daytime ability to function, daytime alertness, and sense of physical well-being also were improved. The effect on sleep was maintained but attenuated; at six months, eszopiclone-treated patients fell asleep approximately 16 minutes faster, had 0.7 fewer nighttime awakenings, and slept 39 minutes longer than placebo-treated patients. No studies have compared eszopiclone with non-drug insomnia therapy, zolpidem, zaleplon, or other sedative hypnotic agents.

Price

A one-month supply of eszopiclone (1-, 2-, or 3-mg tablets) will cost patients approximately $111. This price is slightly higher than the cost of comparable agents, such as zolpidem (5 mg, $81-9) or zaleplon (5 mg, $71), and is much more expensive than older benzodiazepine hypnotics.

Simplicity

The recommended starting dose of eszopiclone is 2 mg at bedtime for patients who can remain in bed for at least eight hours. (2) The dose may be increased to 3 mg at bedtime based on patient response. (1) The starting dose should be reduced to 1 mg for patients with severe liver disease, those taking potent CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin [Biaxin], nelfinavir [Viracept]), and patients older than 65 years. The onset of action of eszopiclone may be delayed if taken with or immediately after a high-fat meal. (1)

Bottom Line

Similar to other hypnotic drugs, eszopiclone treats the symptom of insomnia and not the underlying cause. It offers no advantage over other nonbenzodiazepine hypnotic agents for transient insomnia and it therefore should be considered a second-line agent. As with other drugs in this class, it should not be used routinely. Although labeled for this use, long-term, continuous use of eszopiclone should be reserved for those few patients who require nightly therapy and who are able to afford the drug and tolerate the side effects.

REFERENCES

(1.) Lunesta (package insert). Marlborough, Mass.: Sepracor, Inc., 2004. Accessed online May 2, 2005, at: http://www.lunesta.com/PostedApprovedLabelingText.pdf.

(2.) Eszopiclone (Lunesta), a new hypnotic. Med Lett Drugs Ther 2005;47:17-9.

(3.) Krystal AD, Walsh JK, Laska E, Caron J, Amato DA, Wessel TC, et al. Sustained efficacy of eszopiclone over 6 months of nightly treatment: results of a randomized, double-blind, placebo-controlled study in adults with chronic insomnia. Sleep 2003;26:793-9.

(4.) Zammit GK, McNabb LJ, Caron J, Amato DA, Roth T. Efficacy and safety of eszopiclone across 6-weeks of treatment for primary insomnia. Curr Med Res Opin 2004;20:1979-91.

The Authors

ANDREA M. WESSELL, PHARM.D., B.C.P.S., C.D.E., is assistant professor, and C. WAYNE WEART, PHARM.D., B.C.P.S., is a professor in the Department of Pharmacy and Clinical Sciences, and Department of Family Medicine, Medical University of South Carolina Colleges of Pharmacy and Medicine, Charleston, South Carolina

COPYRIGHT 2005 American Academy of Family Physicians
COPYRIGHT 2005 Gale Group

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