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Azithromycin product information

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    Azithromycin product information


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    GD-AZITHROMYCIN azithromycin dihydrate Product Monograph Page 2 of 74 Table of Contents PART I HEALTH PROFESSIONAL. SUMMARY PRODUCT INFORMATION zithromax 500 mg tablet This information is intended for use by health professionals. 1. Name of the medicinal product. Azithromycin 500 mg Tablets. 2. Qualitative and quantitative. Product Information. marketing authorisation for the medicinal product Azithromycin 500mg Tablets PL 10622. The proposed name of the product is Azithromycin.

    Azithromycin tablets can be applied for the treatment of the following infections, when caused by microorganisms sensitive to azithromycin (see sections 4.4 and 5.1): - acute bacterial sinusitis (adequately diagnosed) - acute bacterial otitis media (adequately diagnosed) - pharyngitis, tonsillitis - acute exacerbation of chronic bronchitis (adequately diagnosed) - mild to moderately severe community acquired pneumonia - skin and soft tissue infections - uncomplicated Chlamydia trachomatis urethritis and cervicitis Considerations should be given to official guidance on the appropriate use of antibacterial agents. Adults In uncomplicated Chlamydia trachomatis urethritis and cervicitis the dose is 1000 mg as a single oral dose. For all other indications the dose is 1500 mg, to be administered as 500 mg per day for three consecutive days. As an alternative the same total dose (1500 mg) can also be administered over a period of five days with 500 mg on the first day and 250 mg on the second to the fifth day. Elderly people The same dose as in adult patients is used for elderly people. Since older people can be patients with ongoing proarrhythmic conditions a particular caution is recommended due to the risk of developing cardiac arrhythmia and torsades de pointes (see section 4.4). Paediatric population Azithromycin tablets should only be administered to children weighing more than 45 kg when normal adult dose should be used. [Posted 08/03/2018]AUDIENCE: Patient, Health Professional, Oncology ISSUE: The antibiotic azithromycin (Zithromax, Zmax) should not be given long-term to prevent a certain inflammatory lung condition in patients with cancers of the blood or lymph nodes who undergo a donor stem cell transplant. Results of a clinical trial found an increased rate of relapse in cancers affecting the blood and lymph nodes, including death, in these patients. We are reviewing additional data and will communicate our conclusions and recommendations when our review is complete. BACKGROUND: The serious lung condition for which long-term azithromycin was being studied called bronchiolitis obliterans syndrome is caused by inflammation and scarring in the airways of the lungs, resulting in severe shortness of breath and dry cough. Cancer patients who undergo stem cell transplants from donors are at risk for bronchiolitis obliterans syndrome. The manufacturer of brand name azithromycin is providing a Dear Healthcare Provider letter on this safety issue to health care professionals who care for patients undergoing donor stem cell transplants. Azithromycin is not approved for preventing bronchiolitis obliterans syndrome.

    Azithromycin product information

    Azithromycin FDA Label - Powder for suspension, tablet film coated., Azithromycin 500mg Tablets - Summary of Product Characteristics - eMC

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  7. See full prescribing information for ZITHROMAX. ZITHROMAX azithromycin 250 mg and 500 mg Tablets and Oral Suspension Initial U. S. Approval 1991.

    • ZITHROMAX-Azithromycin Dihydrate Powder, for Suspension - Pfizer
    • UKPAR for Azithromycin 500mg Tablets PL 10622-0315
    • Zithromax Azithromycin Side Effects, Interactions, Warning, Dosage.

    Effectiveness of ZITHROMAX azithromycin and other antibacterial drugs. *Sections or subsections omitted from the full prescribing information are not listed. buy erythromycin cream Azithromycin is used to treat certain bacterial infections in. This product is available in the. Information is for End User's use only. For full prescribing information, including indications, contraindications, warnings, precautions, and adverse events, please refer to the approved product.

     
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