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Zithromax (Azithromycin)

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Zithromax is a Tablet manufactured by Cipla. It is commonly used for the diagnosis or treatment of Bronchitis, Throat infection, Lung infection, Sexaully transmitted disease, Urinary infections.

Other names for this medication:
Azibiot, Azicin, Azimax, Azimycin, Aziphar, Azithin, Azithrox, Azitral, Azitrin, Azitrix, Azitro, Azitrocin, Azomex, Azycyna, Azyter, Bactrazol, Clearsing, Ilozin, Imbys, Maczith, Medimacrol, Momicine, Naxocina, Odazyth, Orobiotic, Phagocin, Ribotrex, Rozith, Sumamed, Texis, Tremac, Zentavion, Zitrex, Zitrocin, Zitrolid, Zitrotek

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Also known as: Azithromycin


Zithromax is in a group of drugs called macrolide antibiotics. Zithromax fights bacteria in the body. Zithromax is used to treat many different types of infections caused by bacteria, such as respiratory infections, skin infections, ear infections, and sexually transmitted diseases. Zithromax may also be used for purposes other than those listed in this medication guide.

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Zithromax Tablets and other antibacterial drugs, Zithromax Tablets should be used only to treat infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Zithromax Tablets are a macrolide antibacterial drug indicated for the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms in the specific conditions listed below.

Zithromax is an antibiotic used to treat bacterial infections of the nose, throat, lungs, bronchitis, ear, skin, soft tissues, and sexually transmitted genital and urinary infections.

Zithromax is a semi-synthetic macrolide antibiotic of the azalide class. Like other macrolide antibiotics, Zithromax inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit of the bacterial 70S ribosome. Binding inhibits peptidyl transferase activity and interferes with amino acid translocation during the process of translation. Its effects may be bacteriostatic or bactericidal depending of the organism and the drug concentration. Its long half life, which enables once daily dosing and shorter administration durations, is a property distinct from other macrolides.


You should take Zithromax orally with a full glass of water 1 hour before or 2 hours after food. Take Zithromax at the same time every day. Zithromax 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 Zithromax 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 Zithromax 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 or call the Poison Help line at 1-800-222-1222.


Store at room temperature between 59-77 F (15-25 C) away from light and moisture, kids and pets. Do not store the liquid longer than 10 days.

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We contrast results from the mixture model with results from tabulations and from standard logistic regression that are based on fixed cut-points. The present study demonstrates that the tested alpha2-adrenergic receptor ligands affect intraspinal acetylcholine release in the rat evoked by nicotinic receptor mechanisms in vivo, and that they possess binding affinity to nicotinic receptors in vitro. Severe or very severe soil sickness could be proved in four of the sites. Administration of CtsD (Pepstatin A) but not B inhibitor (Ca074-Me), in two mouse CKD models, UUO and chronic ischemia reperfusion injury, led to a reduction in fibrosis. Its possible relation to breech positioning, and the role of sonography for its diagnosis and close follow-up are discussed in the light of the relevant literature. In addition to ionic effects, a tightening of the protein structure at low guanidine hydrochloride concentrations is suggested to be responsible for ribonuclease A inactivation. This clinical trial is registered at as NCT00958217. These results suggest that the methylation status of the core-promoter region is one of the mechanisms to determine the cell-specific expression of the ChM-I gene through the regulation of the binding of Sp3.

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Mechanism of the action and the effectiveness of radon treatment of rheumatoid arthritis of varied activity. Immunocytochemistry (ICC) and real time-PCR results revealed change in the expression profile of EFSCs grown on nanofibrous substrates when compared to those grown on control in epithelial induction condition. The study was conducted in a 613-bed acute and tertiary care university hospital. More than two-thirds of them suffer from mental illness as well. However, improved quality of life in these patients has been obtained with the use of conventional treatment. However, use of contrast agent enabled visualization of saddle embolus in the pulmonary artery on 2-dimensional echocardiography, which was later confirmed on computed tomographic pulmonary angiography. The evaluation project enrolled child care centers with families representing the ethnically diverse communities in which they were located.

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Social and financial considerations are often integrated when real life decisions are made, and recent studies have provided evidence that similar brain networks are engaged when either social or financial information is integrated. Concurrent administration of 0.1 mg CB-154 to the estrogen-treated mice significantly reduced the incidence of mammary tumors when compared with mice treated with the steroid alone. A variety of occupational peculiarities results in a higher morbidity of workers. These findings reveal that leptin mobic meloxicam drug class activates Hh signaling to alter gene expression programs that control cell fate and have important implications for liver fibrosis and other leptin-regulated processes involving EMTs, including development, obesity, and cancer metastasis. Moreover, the overproduction of Rrb1p led to increases in cellular levels of free rpL3 that accumulated in the nucleus together with Rrb1p. Lung DC bridge innate and adaptive immunity, and depending on the context, induce Th1, Th2 or Th17 response, to optimally clear infections. We achieved implantation into a superficial cortical vein overlying the motor cortex via catheter angiography and demonstrate neural recordings in freely moving sheep for up to 190 d. During the last decades, numerous large-scale epidemiological studies have identified Hcy as a moderate independent cardiovascular risk factor. In conclusion we find scalp closure with Kirschner wires are a simple and effective method for scalp wound closure. Specific signaling pathways, including RhoA and PI3 kinase, mediated observed processes and specific inhibitors of these pathways prevented ROS-induced monocyte migration across an in vitro model of the BBB.

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OBJECTIVE: To evaluate and compare the effects of lisinopril versus atenolol administration on the diurnal blood pressure profile and the nocturnal blood pressure fall in young mild-to-moderate essential hypertensives.METHODS: Thirty patients were studied. Measurement of particulate phase polycyclic aromatic hydrocarbon (PAHs) around a petroleum refinery. The third patient, a woman with chronic lymphoma in remission, was receiving topical antibiotics and corticosteroids for a corneal transplant performed one year previously. Such geometrical reorganization allows many dyneins within a cluster to generate cooperative force on a single microtubule. The clinical significance of stratifying cardiovascular risk in hypertensive patients on the basis of retinal changes such as arteriolar narrowing or arterio-venous crossing has been criticized. This protein transfer from epididymosomes to spermatozoa is time-dependent, temperature-dependent and pH-dependent, and is more efficient in the presence of zinc. Despite a large body of genetic and biochemical data indicating that myc proteins are located in the nucleus and can bind to nucleic acids, the mechanism by which these proteins exert their effects remains a mystery. The included studies were analyzed for neuroprotection and methodology.

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