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Azitrovid (Azithromycin)

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Azitrovid is an antibiotic medication. It is commonly given to children for the treatment of a wide range of bacterial infections targeting the ear, eyes, nose, throat, lungs, skin, and gastrointestinal tract.

Other names for this medication:
Atizor, Azithromycin, Azitrix, Azitro, Azitrocin, Azitrom, Azitromicina, Azitrox, Azomax, Azrolid, Clearsing, Gramokil, Macromax, Maczith, Mezatrin, Neblic, Novatrex, Novozitron, Opeazitro, Phagocin, Tromic, Tromix, Zibac, Zibramax, Zifin, Zimax, Zirocin, Zitroneo, Zitrotek

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Also known as: Azithromycin


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

Azitrovid 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.

Azitrovid 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.

Azitrovid is a semi-synthetic macrolide antibiotic of the azalide class. Like other macrolide antibiotics, Azitrovid 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 Azitrovid exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended. The dose and length of treatment with azithromycin may not be the same for every type of infection.

Azitrovid can be taken with or without food.

Shake the oral suspension (liquid) well just before you measure a dose. Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one.

Use this medicine for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Azitrovid will not treat a viral infection such as the flu or a common cold.

Store at room temperature away from moisture and heat. Throw away any unused liquid medicine after 10 days.

Detailed Azitrovid dosage information


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


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 Zmax® extended-release oral suspension. 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 Azitrovid® 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.

Detailed Azitrovid dosage information

Side effects

The most common side effects associated with Azitrovid 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.


Ketolide allergy. History of cholestatic jaundice/hepatic dysfunction associated with prior use.

Pneumonia: oral treatment is for mild, community-acquired cases suitable for outpatient therapy only. Discontinue if signs/symptoms of hepatitis occur. Known QT prolongation, proarrhythmic conditions, clinically significant bradycardia: avoid. Allergic symptoms may recur after initial successful symptomatic treatment. Myasthenia gravis. Hepatic or renal impairment. Elderly. Pregnancy (Cat.B). Nursing mothers.

Avoid concomitant aluminum- or magnesium-containing antacids. Monitor with digoxin, phenytoin, warfarin. Monitor for azithromycin toxicity (eg, liver dysfunction, ototoxicity) with nelfinavir. Concomitant Class 1A (eg, quinidine, procainamide), or Class III (eg, dofetilide, amiodarone, sotalol) antiarrhythmics, or others known to prolong the QT interval: avoid.

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Associations of a sexually transmitted disease diagnosis during a relationship with condom use and psychosocial outcomes: (short) windows of opportunity. To determine the role of GC79, we cloned its complementary DNA (cDNA) and functionally characterized its product. Effects of the hepatocarcinogen 2-aminofluorene on RNA synthesis in rat liver. The metabolism of 3,5,5-trimethylcyclohexyl mandelate (Cyclandelate) (III). Althuogh extremely rare, primary gastric actinomycosis should be considered in the differential diagnosis of radiologic and gastroscopic diffuse gastric wall thickening and submucosal tumor-like or infiltrative lesions, particularly in patients with history of abdominal surgery or trauma, or those receiving extensive medication. Isolation of giant unilamellar vesicles from electroformed vesicle suspensions and their extrusion through nano-pores. The overall incidence of JE cases was 15 per 10,000 children aged 5-9 years, and the estimated ratio overt:inapparent infection was 1:270.

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Proton therapy favorably spares normal tissue without compromising target coverage. We investigated the interrelation of three known effector mechanisms of the cellular response to periodontal infection, namely reactive oxygen species (ROS), matrix metalloproteinases (MMPs) and cytokines in primary cell cultures of human periodontal ligament fibroblast (hPDLF). The family of magnetoactive compounds Cu(hfac)(2)L(R) exhibits thermo- and photoswitching phenomena promising for various applications. Myomodulin-CARP-family peptides have been isolated only from molluscs. A total of 10,146 participants were included in the analyses of cholesterol and C-reactive protein and 4,461 in the analyses of fibrinogen. Opioids are generally the primary class of analgesic prescribed, but because of associated side effects during long-term treatment, many patients become noncompliant or discontinue treatment.

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Proteasome-dependent proteolysis has a critical role in fine-tuning the feedback inhibition of cytokinin signaling. Tetramethylammonium hydroxide-assisted thermochemolysis performed in an off-line mode proved a useful tool in determining organic compounds in the effluent from laboratory-scale phytoremediation systems. MR imaging showed the lesion to have low signal intensity on T1-weighted images and intermediate signal intensity on T2-weighted images. Therefore the adalat cc medication aim of this study was to evaluate the correlation of BDNF in serum of FMS with intensity of depression and anxiety. There were no differences in penetration of cells by inhibitor, rate of enzyme-inhibitor combination, affinity of inhibitor or substrate for the cholinesterase, or protective effect of substrate upon the enzyme. Tests of nonlinearity and a random shuffling routine revealed deterministic and nonlinear portions in the fetal ECoG. Oxyl radicals, redox-sensitive signalling cascades and antioxidants.

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A conversation with 2009 Caring Award winner: General Colin Powell. Primary outcome was infection, bacterial sensitivity pattern, amputation, flap failure and union of the fracture. Intraoperative tremor monitoring for vitreoretinal microsurgery. Carbohydrate composition of serum transferrin isoforms from patients with high alcohol consumption. Recognition of the positive results that have been achieved by behavioral sciences can be important in reducing the psychological and behavioral burden of gynecologic cancer. Adolescents are a heterogeneous, vulnerable, and sexually active group. Using sera from HIV-1-infected clomid medication effectiveness individuals at a variety of disease states, three major epitopes were identified within p17 and one within p24.

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In preliminary cytotoxicity studies used to determine appropriate test concentrations for chromosomal aberration analysis, the LC50 of Et3PbAc was approximately 10 microM in the absence of metabolic activation, and 80 microM in the presence of metabolic activation. However, much remains to be clarified, particularly the meaning of the time-dependent shifts in the location of the trace, and the ways in which these molecular and cellular events translate into changes in behavior in the animal. Fracture healing and preservation of motion of adjacent joints was achieved in all cases with internal fixation using the plating techniques described by the A-O group. These reagents lose much of their ability to neutralize the C polysaccharide toxin when superinjected after an interval of 4 hours following toxin injections. The histologic parameters were graded semiquantitatively and compared preoperatively and postoperatively. The specific maize MDH involved was identified by mass spectrometry (ESI-QTOF-MS/MS, MALDI-TOF-MS). Gene silencing, first observed in plants containing transgenes, can operate both at the transcriptional and post-transcriptional levels.

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Peroxisome proliferator-activated receptor (PPAR)-gamma expression in human vascular smooth muscle cells: inhibition of growth, migration, and c-fos expression by the peroxisome proliferator-activated receptor (PPAR)-gamma activator troglitazone. Nevertheless, stress due to surgical procedures induces physiological responses in clinical settings. At 49 d, 16 birds from each room were processed to determine weights and yields. Phase I study of fludarabine plus cyclophosphamide in patients with previously untreated low-grade lymphoma: results and and long-term follow-up--a report from the Eastern Cooperative Oncology Group. ICP is one of the most important intensive types of monitoring for patients with moderate-to-severe bifrontal contusions and may be beneficial in creating a better prognosis. The cytokinesis block micronuclei test in V79 cells induced by mitomycin, the test of metabolic cooperation between V79 and M cells and the test of growth ability of Hela cells in soft agar were used in the screening. In microcirculation it manifests multiple insults, including leukocyte and platelet adhesion, ROS and protease overproduction, mast cell degranulation, endothelium hyperpermeabilty, hemorrhage, and microthrombi formation, ultimately results in multiorgan dysfunction, DIC, refractory shock and even death. Serum cortisol levels in very low birth weight infants of substance-abusing mothers. To determine mortality independent predicting factors, a lipitor high dose side effects logistic regression model was used.

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