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Azilide (Azithromycin)

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Azilide is used for treating mild to moderate infections caused by certain bacteria. It may also be used alone or with other medicines to treat or prevent certain infections in persons with advanced HIV infection. Azilide is a macrolide antibiotic. It slows the growth of, or sometimes kills, sensitive bacteria by reducing the production of important proteins needed by the bacteria to survive.

Other names for this medication:
Azatril, Azigram, Azilide, Azimed, Azinom, Azithrex, Azithromax, Azithromycin, Azithrox, Azithrus, Azitrocin, Azitropharma, Azitrotek, Azitrox, Azomax, Azomex, Azomycin, Azycyna, Azyter, Azyth, Binozyt, Iramicina, Neblic, Respazit, Rozith, Talcilina, Tridosil, Ultrabac, Zemycin, Zibramax, Zinfect, Zitroken, Zival, Zocin

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Also known as: Azithromycin


Azilide (Azilide tablets and Azilide for oral suspension) contain the active ingredient azithromycin, a macrolide antibacterial drug, for oral administration. Azilide has the chemical name (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[(2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl) oxy]-2-ethyl-3,4,10-trihydroxy-3,5,6,8,10,12,14-heptamethyl-11-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-1-oxa-6-azacyclopentadecan-15-one. Azilide is derived from erythromycin; however, it differs chemically from erythromycin in that a methyl-substituted nitrogen atom is incorporated into the lactone ring. Its molecular formula is C38H72N2O12, and its molecular weight is 749.00.

Azilide, as the dihydrate, is a white crystalline powder with a molecular formula of C38H72N2O12∙2H2O and a molecular weight of 785.0.

Azilide is supplied as tablets containing azithromycin dihydrate equivalent to either 250 mg or 500 mg azithromycin and the following inactive ingredients: dibasic calcium phosphate anhydrous, pregelatinized starch, sodium croscarmellose, magnesium stearate, sodium lauryl sulfate, hypromellose, lactose, titanium dioxide, triacetin, and D&C Red #30 aluminum lake.

Azilide for oral suspension is supplied in bottles containing azithromycin dihydrate powder equivalent to 300 mg, 600 mg, 900 mg, or 1200 mg azithromycin per bottle and the following inactive ingredients: sucrose; sodium phosphate, tribasic, anhydrous; hydroxypropyl cellulose; xanthan gum; FD&C Red #40; and spray dried artificial cherry, creme de vanilla, and banana flavors. After constitution, each 5 mL of suspension contains 100 mg or 200 mg of azithromycin.


You should take Azilide orally with a full glass of water 1 hour before or 2 hours after food. Take Azilide at the same time every day. Azilide treats different types of bacterial infections and can be used both by adults and by children. For children: The dosage is dependent upon the child's weight. In treatment of otitis media, take Azilide for 1-5 days. For adults: To treat pneumonia or throat/tonsil infection, the recommended dose is two 250 mg tablets on the first day and then one 250 mg tablet once a day for 4 more days. For the prevention of MAC (mycobacterium avium complex), the recommended dosage of Azilide is 1,200 mg per week. For the treatment of skin or infections, the recommended dosage is two 250 mg tablets on the first day and one 250 mg tablet for another 4 days.


Seek emergency medical attention if you think you have used too much of this medicine. Symptoms of an Azilide overdose may include nausea, vomiting, diarrhea, and stomach discomfort.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) and away from excess moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Azilide are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Do not use Generic Azilide if you are allergic to Generic Azilide components.

Do not take Generic Azilide at the same time with antacid contained magnesium or aluminum.

Try to be careful with Generic Azilide while you are pregnant or have nurseling.

Try to be careful with Generic Azilide usage in case of having liver or kidney disease, Long QT syndrome, heart rhythm problems.

Try to be careful with Generic Azilide usage in case of taking cyclosporine (Neoral, Sandimmune), anticoagulants ('blood thinners') such as warfarin (Coumadin), terfenadine (Seldane), digoxin (Lanoxin), dihydroergotamine (D.H.E. 45, Migranal), ergotamine (Ergomar), phenytoin (Dilantin), medications that suppress your immune system, nelfinavir (Viracept).

Try to be careful with Generic Azilide usage in case you are allergic to erythromycin (E.E.S., E-Mycin, Erythrocin), dirithromycin (Dynabac), clarithromycin (Biaxin), azithromycin.

Try to be careful with sunbeams. Generic Azilide makes skin sensitive to sunlight. Protect skin from the sun.

Generic Azilide can be taken by children.

It can be dangerous to stop Generic Azilide taking suddenly.

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Poisson regression analyses were conducted on 11.7 million years of follow-up of 25-59 year old New Zealand census respondents spanning four separate cohort studies (1981-1984, 1986-1989, 1991-1994, and 1996-1999). The histologic findings of both the facial lesions and the pigmented macules of the penis in the Bannayan-Riley-Ruvalcaba syndrome have not, to our knowledge, been reported previously. Dual action of retinoic acid on human embryonic/fetal hematopoiesis: blockade of primitive progenitor proliferation and shift from multipotent/erythroid/monocytic to granulocytic differentiation program. Microemulsion technology in the reformulation of cyclosporine: the reason behind the pharmacokinetic properties of Neoral. A number of studies have observed an increased incidence of treatment-related leukemias following chemotherapy with alkylating agents and/or topoisomerase II inhibitors. Intravenous glucose tolerance tests were performed in 39 normal controls and 46 first-degree relatives. Health-care providers should play an important role in promoting, counseling and health education regarding HRT needs to rectify these problems. The Iowa Dentist Tracking System (IDTS) was used to collect demographic, educational, practice arrangement, office location and work hour data for all active Iowa dentists beginning in 1997.

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Mice in which LC had regressed due to this combination therapy showed an antitumor delayed hypersensitivity reaction (measured by the footpad test), but they were not resistant to rechallenge with LC. Non-invasive registration of the aboral and oral spreading of the gastroduodenal peristaltic activity (experimental and clinical investigations). Inhibition mechanisms of staurosporine and H7 to cAMP-dependent protein kinase have been investigated through docking studies. Cord venous concentrations of angiotensin II were significantly greater than those in cord arterial blood in babies delivered vaginally but not in those delivered by lower-segment Caesarean section. Some treated normal quail fell into dysstasia and died of nutritional disturbances. The supposed antagonists (S)-2-methyl-2-amino-4-phosphonobutanoate (MAP4) and (RS)-alpha-methyl-4-phosphonophenylglycine (MPPG), have a predominantly proconvulsant effect. On the absorption of proscillaridin A after single oral doses to normal and achlorhydric subjects. Changes in the activity of transport Ca-ATPase in osmotically disrupted synaptosomes were studied in corazol-induced generalized epileptic activity (EA) monitored by biaxin usual dosage electrocorticogram.

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Immunohistochemical procedures for dystrophin analyses were performed using monoclonal antibodies for three different domains. The repair of gamma-ray-induced chromosomal damage in human lymphocytes after exposure to extremely low frequency electromagnetic fields. It has been used successfully to detect influenza outbreaks at an early stage. The specific accumulation of GFP in guard cell chloroplasts, their tubular connections, the translocation of the precursor polypeptide into the different types of organelles, as well as the use of a plastid-targeted GFP protein as a versatile marker is discussed in the flagyl 500 ovule pour quel infection context of previously described observations. A review on treatment of bleeding peptic ulcer: a collaborative task of gastroenterologist and surgeon. However, studies of BAFF in teleosts are very limited and its function, in particular that under in vivo conditions, is essentially unknown.

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Application of technique of labeling BMSCs with PKH26 to tissue engineered bone construction. Radiation protection by sulfhydryl compounds and their paramagnetic properties after x-irradiation in relation to their chemical structure. Histopathologic evaluation of cutaneous lesions in scleredema adultorum. Clinico-morphological characteristics of injuries inflicted by shots from weapons of non-lethal action. The transient absorption studies show that the J will flagyl cause a yeast infection -aggregate improves the photoinduced charge separation at the porphyrin/TiO2 interface. The aim of the current study was to assess possible postconditioning with sevoflurane in an in vivo model of endotoxin-induced lung injury.

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