Zithromax (azithromycin)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Azithromycin is an azalide antibiotic, a subclass of macrolide antibiotics.
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Generic name: azithromycin
Pronunciation: (ay-ZITH-roe-MYE-sin)
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Zithromax
Indications
The following indications are listed for Zithromax:
- Bacterial Pneumonia
- Chlamydia Trachomatis Pelvic Inflammatory Disease
- Chlamydial Pneumonia
- Haemophilus Influenzae Pneumonia
- Legionella Pneumophila Pneumonia
- Moraxella Catarrhalis Pneumonia
- Mycoplasma Hominis Pelvic Inflammatory Disease
- Mycoplasmal Pneumonia
- Pelvic Inflammatory Disease With Neisseria Gonorrhea
- Pneumococcal Pneumonia
- Pneumonia Due To Staphylococcus Aureus
Also known as: Eaton Agent Pneumonia, H. Flu Pneumonia, H. Influenzae Pneumonia, Hemophilus Influenzae Pneumonia, Infection Of The Lungs Due To Chlamydia, Influenza Bacillus Pneumonia, Pelvic Inflammatory Disease Due To Chlamydia Trachomatis, Pelvic Inflammatory Disease Due To Mycoplasma Hominis, Pelvic Inflammatory Disease Due To Neisseria Gonorrhea, Pfeiffer's Bacillus Pneumonia, Pid Due To Chlamydia Trachomatis, Pid Due To Mycoplasma Hominis, Pneumonia Due To B. Catarrhalis, Pneumonia Due To Branhamella Catarrhalis, Pneumonia Due To Haemophilus Influenzae, Pneumonia Due To M. Catarrhalis, Pneumonia Due To Moraxella Catarrhalis, Pneumonia Due To Neisseria Catarrhalis, Pneumonia Due To Staphylococcus Pyogenes Aureus, Pneumonia Due To Streptococcus Pneumoniae, Primary Atypical Pneumonia.
Dosing
Pending revision, the material in this section should be considered in light of more recently available information in the MedWatch notification at the beginning of this monograph.
Dosage of azithromycin, which is commercially available for oral and IV use as the dihydrate, is expressed in terms of anhydrous azithromycin.
Two 250-mg tablets of azithromycin are bioequivalent to one 500-mg tablet. The extended-release oral suspension is not bioequivalent to and is not interchangeable with the conventional oral suspension or tablets.
Dosage adjustment is not necessary in patients with renal impairment (glomerular filtration rate 80 mL/minute or less). However, data are limited regarding use of azithromycin in patients with severe renal impairment (glomerular filtration rate less than 10 mL/minute) and the manufacturer states that the drug should be used with caution in these patients.
The pharmacokinetics of azithromycin in patients with hepatic impairment have not been established. The manufacturer states that data are insufficient to make dosage recommendations for patients with hepatic impairment and azithromycin should be used with caution in such patients since the drug is eliminated principally via the liver. Based on results of a limited study in patients with impaired hepatic function, some clinicians state that dosage adjustments are not necessary in patients with class A or B liver cirrhosis.
No dosing information is available for this tab.
No dosing information is available for this tab.
No dosing information is available for this tab.
Drug interactions
There is no enhanced messaging for this drug.
There are no contraindication interactions for this drug.
There are no severe interactions for this drug.
There are no moderate interactions for this drug.
Contraindications
There is no enhanced messaging for this drug.
There are no contraindication contraindications for this drug.
There are no severe contraindications for this drug.
There are no moderate contraindications for this drug.
Adverse reactions
There is no enhanced messaging for this drug.
There are no severe adverse reactions for this drug.
There are no less severe adverse reactions for this drug.
Precautions
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No enhanced messaging available.
Reproduction studies in rats and mice using azithromycin dosages up to 200 mg/kg daily (approximately equivalent on a mg/m2 basis to 4 and 2 times, respectively, the human daily oral azithromycin dosage of 500 mg; to 2 or 1 times, respectively, the 1.2-g weekly dosage used for prevention of M. avium complex infection; or 3.3 or 1.7 times, respectively, the 600-mg daily oral dosage used for the treatment of M. avium complex) have not revealed evidence of harm to the fetus. However, there are no adequate and controlled studies to date using azithromycin in pregnant women, and the drug should be used during pregnancy only when clearly needed.
Preliminary data indicate that azithromycin may be safe and effective in the treatment of chlamydial infections in pregnant women; however, there are insufficient data to recommend routine use of the drug during pregnancy. (See Chlamydial Infections: Urogenital Chlamydial Infections, in Uses.) Azithromycin is considered the drug of choice for Mycobacterium avium complex (MAC) prophylaxis in HIV-infected pregnant women. (See Mycobacterium Avium Complex (MAC) infections: Prevention of Disseminated MAC Infection, in Uses.)
Azithromycin has been detected in human milk. The drug should be used with caution in nursing women.
No enhanced messaging available.
ICD codes
No ICD codes are available for this drug.
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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