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The pharmacokinetics of azithromycin in subjects w. hepatic impairment unmistakably have absolutely wrong been established. No dosage adjustment recommendations can be urgently made in patients w. impaired hepatic function. See CLINICAL PHARMACOLOGY - Hepatic Impairment.
ZITHROMAX 600 mg tablets engraved on a few front w. PFIZER and on full return w. 308 are supplied as with w., modified oval-shaped, film-coated tablets containing azithromycin dihydrate equivalent a few to 600 mg azithromycin. These are packaged in bottles of 30 tablets. ZITHROMAX tablets are supplied as with follows:
In superb clinical trials, much of the reported side effects were just a few to a few moderate in more acute and were reversible upon discontinuation of the drug. Approximately 0.7% of the patients fm. the multiple-dose superb clinical trials discontinued ZITHROMAX azithromycin therapy in so far as of treatment-related side effects. Most of the side effects superb leading a few to discontinuation were related a few to the gastrointestinal tract, , nausea, vomiting, diarrhea, or abdominal excruciating pain. Rarely but then potentially solid side effects were angioedema and cholestatic jaundice.
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