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Azithro (Azithromycin)

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Azithro is created by pharmacy specialists to struggle against dangerous infections (STD, pneumonia, bronchitis, lungs, throat or ears infections, skin infections, MAC). Target of Generic Azithro is to control, ward off and terminate bacteria.

Other names for this medication:
Azicip, Azimed, Azimycin, Azinix, Aziphar, Azithromycin, Azithrus, Azomac, Aztrin, Azyth, Bactrazol, Goldamycin, Goxil, Hemomycin, Neblic, Odazyth, Ordipha, Orobiotic, Ricilina, Sitrox, Texis, Triamid, Tritab, Zentavion, Zibac, Zifin, Zistic, Zithrin, Zithrocin, Zitrex, Zitrolid

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Also known as: Azithromycin


Azithro is in a group of drugs called macrolide antibiotics. Azithro fights bacteria in the body. Azithro is used to treat many different types of infections caused by bacteria, such as respiratory infections, skin infections, ear infections, and sexually transmitted diseases. Azithro 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 Azithro Tablets and other antibacterial drugs, Azithro 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.

Azithro 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.

Azithro 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.

Azithro is a semi-synthetic macrolide antibiotic of the azalide class. Like other macrolide antibiotics, Azithro 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.


Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. The dose and length of treatment with Azithro may not be the same for every type of infection. Take each tablet or capsule with a full glass (8 ounces) of water. To use the oral suspension single dose packet: Open the packet and pour the medicine into 2 ounces of water. Stir this mixture and drink all of it right away. To make sure you get the entire dose, add a little more water to the same glass, swirl gently and drink right away. Azithro capsules must be taken on an empty stomach. Take the capsule at least 1 hour before or 2 hours after eating a meal Azithro tablets or powder oral suspension may be taken with or without food. Take the tablet or oral suspension with food if the medicine upsets your stomach. Do not take Azithro at the same time as taking an antacid that contains aluminum or magnesium. This includes Rolaids, Maalox, Mylanta, Milk of Magnesia, Pepcid Complete, and others. These antacids can make Azithro less effective when taken at the same time. Shake the oral suspension (liquid) well just before you measure a dose. To be sure you get the correct dose, measure the liquid with a marked measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one. Take this medication for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Azithro will not treat a viral infection such as the common cold or flu. It is important to take Azithro regularly to get the most benefit. Store this medication at room temperature away from moisture and heat. Throw away any unused liquid medicine after 10 days.


If you overdose Azithro and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Azithro overdosage: discomfort feeling in stomach, diarrhea, retching, nausea.


Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Do not refrigerate or freeze the extended-release oral liquid. After water has been added to the powder, use the dose within 12 hours and throw away any unused liquid after your dose.

You may store the oral liquid at room temperature or in the refrigerator. Do not freeze the bottle. Do not keep the oral liquid for more than 10 days. Throw away any unused liquid after all doses are completed.

Side effects

The most common side effects associated with Azithro 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.


You are allergic to any ingredient in Azithro, to other macrolide antibiotics (eg, erythromycin), or to ketolide antibiotics (eg, telithromycin).

You are taking dofetilide, nilotinib, pimozide, propafenone, or tetrabenazine.

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METABOLIC AND MORPHOLOGICAL ADAPTATION TO HETEROGENOUS ENVIRONMENTS BY THE PACIFIC TREE TOAD, HYLA REGULA. This retrospective study was designed to investigate the use of equine amniotic membrane transplants (AMT) at preserving vision, maintaining the structural integrity of the globe and maximizing cosmesis in equine eyes with corneal ulceration and severe keratomalacia. A research was conducted in the electronic bibliographic databases Cochrane, MEDLINE, and EMBASE. Poorly differentiated NECs have a high mutation burden with potentially targetable mutations. The morphology of apoptotic PC-3M cells was observed by electron microscopy. The categories identified by restriction analysis of PCR-amplified cDNA corresponded with serogroups established by plaque-reduction neutralization tests. Agreement between the calculated and experimental values was satisfactory, indicating the reliability of the proposed method. Persistence of Racial and Ethnic Differences in Utilization and Adverse Outcomes of Total Joint Replacement. Death by apoptosis would ensure the rapid removal of injured neurons, whereas conditions that prevent apoptosis may facilitate the persistence of damaged cells and favor inflammation and disease progression. Microbial film formation: dental plaque deposition on acrylic tiles using continuous culture techniques.

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These data suggest that viral particles may persist in shellfish tissues for several weeks. Insertion behavior of miniature IBW-79 pressure transducers in the left heart. Comparison of the aqueous solubilization of practically insoluble niclosamide by polyamidoamine (PAMAM) dendrimers and cyclodextrins. Time-activity FDG heart, lung, liver and blood data from paired fasting and glucose-loaded sessions in five adult human volunteers, together with published brain parameters, were incorporated into a multicompartmental model for whole-body FDG kinetics. We used electrophysiological methods to track the deployment of visual spatial attention while observers were engaged in concurrent central attentional processing, using a variant of the attentional blink xalatan eye drops storage temperature paradigm. Hash-Based Line-by-Line Template Matching for Lossless Screen Image Coding. We conclude that 3 mo of multivitamin and mineral supplementation was without any measurable ergogenic effect. A total of 14 cows was immunized with single strains of heat-killed oral bacteria or pools of strains of Actinomyces, Porphyromonas, Prevotella, and Fusobacterium. Together these data show that EVs from stroke patients are proinflammatory in nature and are capable of inducing inflammation in immune cells. The result for Fraunhofer diffraction of monochromatic radiation is well known, and this work reports the result for radiation from a Planckian source.

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