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Azithrex

Doctors most often prescribe penicillin or Azithrex to treat strep throat. They are the top choices because they're safer, inexpensive, and they work well on strep bacteria.

Other names for this medication:
Amovin, Azadose, Azalid, Azicine, Azifast, Azilide, Azimac, Azimycin, Azinom, Azithrex, Azithrox, Azithrus, Azitrocin, Azitropharma, Azomycin, Azyter, Clearsing, Disithrom, Ezith, Faxin, Hemomycin, Ilozin, Iramicina, Koptin, Magnabiotic, Mezatrin, Neblic, Neofarmiz, Novozithron, Respazit, Ricilina, Sitrox, Talcilina, Tromic, Ultrabac, Vectocilina, Zertalin, Zicho, Zimax, Zithrocin, Zithromac, Zitrex, Zitrofar, Zitrolid, Zitromax, Zitroneo, Zitrotek, Zycin

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Also known as: Azithromycin

Description

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

Azithrex is the local analog (generic) of more famous drug Azithrex that has the same active substance (ingredient) and in result the same therapeutic effect. The main difference is that Azithrex is registered by a small local pharmaceutical company. The presence of the same active substance guarantees an identical pharmaceutical (therapeutic) effect on the body.

It is possible to buy Azithrex only in the pharmacies of the country where it is produced. With us, you can buy its more famous analog Azithrex, which is approved by the FDA and is sold worldwide. The same active substance guarantees the identity of the drugs and the identity of the pharmaceutical properties (they have only different names and packaging, in which they are sold).

Dosage

This section provides information on the proper use of a number of products that contain azithromycin. It may not be specific to Azithrex Tri-Pak. Please read with care.

Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.

This medicine comes with a patient information leaflet. Read and follow the instructions carefully. Ask your doctor if you have any questions.

You may take Azithrex® oral liquid or tablets with or without food.

Shake well the bottle of Azithrex® oral liquid before each use. Measure your dose correctly with a marked measuring spoon, oral syringe, or medicine cup. The average household teaspoon may not hold the right amount of liquid.

Measure the Zmax® extended-release oral suspension with a marked measuring spoon, syringe, or cup. You or your child must take this medicine within 12 hours after it has been mixed with water. It is best to take the Zmax® extended-release oral suspension on an empty stomach or at least 1 hour before or 2 hours after a meal. If your child does not use all of the medicine in the bottle, throw it away after you give the dose.

If you or your child vomits within one hour of taking the Zmax® extended-release oral suspension, call your doctor right away to see if more medicine is needed.

Keep using this medicine for the full treatment time, even if you or your child feel better after the first few doses. Your infection may not clear up if you stop using the medicine too soon.

If you are taking aluminum or magnesium-containing antacids, do not take them at the same time that you take Azithrex®. These medicines may keep azithromycin from working properly. However, you can take antacids with Zmax®.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For oral dosage form (extended-release suspension): For treatment of pneumonia: Adults—2 grams (g) once as a single dose. Children weighing 34 kilograms (kg) or more—Dose is based on body weight and must be determined by your doctor. The dose is usually 2 grams once a day, taken as a single dose. Children 6 months of age and older weighing less than 34 kg—Dose is based on body weight and must be determined by your doctor. The dose is usually 60 milligrams (mg) per kilogram (kg) of body weight once a day, taken as a single dose. For treatment of sinusitis: Adults—2 grams (g) once a day as a single dose. Children—Use and dose must be determined by your doctor. For oral dosage forms (suspension or tablets): For treatment of infections: Adults—500 to 2000 milligrams (mg) once a day, taken as a single dose. Depending on the type of infection, this may be followed with doses of 250 to 500 mg once a day for several days. Children 6 months of age and older—Dose is based on body weight and must be determined by your doctor. The dose is usually 10 to 30 milligrams (mg) per kilogram (kg) of body weight once a day, taken as a single dose. Depending on the type of infection, this may be followed with doses of 5 to 10 mg per kg of body weight once a day for several days. Children younger than 6 months of age—Use and dose must be determined by your doctor. For treatment of pharyngitis or tonsillitis: Adults—500 milligrams (mg) on Day 1 (the first day), taken as a single dose. Then, 250 mg on Day 2 through Day 5. Children 2 years of age and older—Dose is based on body weight and must be determined by your doctor. The dose is usually 12 milligrams (mg) per kilogram (kg) of body weight once a day for 5 days. Children younger than 2 years of age—Use and dose must be determined by your doctor.

Overdose

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

Storage

Store Azithrex below 86 degrees F (30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Azithrex out of the reach of children and away from pets.

Side effects

The most common side effects associated with Azithrex 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.

Contraindications

You should not use Azithrex Z-Pak if you are allergic to it, or if you have ever had:

jaundice or liver problems caused by taking Azithrex Z-Pak; or a severe allergic reaction to similar drugs such as clarithromycin, erythromycin, or telithromycin.

Azithrex Z-Pak oral should not be used to treat pneumonia in people who have:

cystic fibrosis; an infection after being in a hospital; an infection in the blood; a weak immune system (caused by diseases such as HIV/AIDS or cancer); or in older adults and those who are ill or debilitated.

Tell your doctor if you have ever had:

pneumonia; liver or kidney disease; myasthenia gravis; low levels of potassium in your blood; a heart rhythm disorder; or long QT syndrome (in you or a family member).

It is not known whether this medicine is effective in treating genital ulcers in women.

Tell your doctor if you are pregnant or breastfeeding. Taking Azithrex Z-Pak while breastfeeding may cause diarrhea, vomiting, or rash in the nursing baby.

Azithrex Z-Pak is not approved for use by anyone younger than 6 months old. This medicine should not be used to treat a throat or tonsil infection in a child younger than 2 years old.

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Cell viability and proliferation was analysed (XTT and BrdU assay) after 24 h and flowcytometric cell cycle analysis was performed after 24 and 48 h. Analysis of such high-dimensional feature vectors are complex and time consuming. Combined genotypic and phenotypic analyses of clinical isolates revealed the presence of moderate levels of phenotypic resistance (between 4- and 50-fold) to 3TC in a subset of isolates that did not harbor the M184V mutation. In addition, chimeric analyses and conditional removal of Wnt3 activity reveal that Wnt3 expression in the epiblast is required for induction of the primitive streak and mesoderm whereas activity in the posterior visceral endoderm is dispensable. Modal analysis of the designed UEVC device was performed by using the finite element method, which shows that the resonant frequencies coincide well with the targeted ones. The reaction strictly requires a region of mismatch in the duplex, which may serve as a nucleation site for RecA protein polymerization. Death caused by myocardial ischemia occurred after surgical closure of VSD and PDA. The aim of this study was to evaluate in-hospital mortality and during follow-up of diabetic patients with acute myocardial infarction treated with primary angioplasty and to determine its predictors. Disaster events and the risk of sudden cardiac death: a Washington State investigation. For one of our patients, a medical treatment allowed us to perform a liver transplantation.

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We find that the compound melphalan shows two different drift times due to the formation of gas-phase charge isomers (protomers). From the MORTH database, data availability on safety performance indicators was 60 percent at both national and state levels. However, the mechanisms through which monocytes/macrophages interact with osteoblasts are still elusive. Sibrafiban versus Aspirin to Yield Maximum Protection from Ischemic Heart Events Post-acute Coronary Syndromes. As cardiac diseases and cancer remain the first and second causes of mortality in developed nations, respectively, cardio-oncology is the answer to this group of individuals who are especially vulnerable to both causes of mortality. The most important factors influencing the choice of method of re-surgery were the type of the previous operation, the results of urodynamic studies, and the preference and experience of the surgeon. Clinical study of the correlation among the levels of human corticotropin-releasing hormone, c-Fos and connexin-43 at onset of labor. Udder health of heifers deserves the attention of cattle farmers and veterinarians.

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Furthermore, the birthweight/placental weight ratio is increased in these pregnancies, consistent with fetal growth restriction, and is higher with a male fetus than with a female fetus. Centrosome division was synchronous throughout the embryo and the period of the uncoupled duplication cycle increased over successive divisions. Whole-body 16-MDCT and neck MDCTA can be used to diagnose blunt cerebrovascular injuries with comparable accuracy. Peripheral tolerance is required to maintain balance within the immune system. Venom-injecting structures have arisen independently in unrelated arthropods including scorpions, spiders, centipedes, larval owlflies and antlions, and Hymenoptera (wasps, ants, and bees). Despite methodological advances in the field of economic evaluations of interventions, economic evaluations of obesity prevention programmes in early childhood are seldom conducted. Construction and characterization of bidirectional expression vectors in Saccharomyces cerevisiae.

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A Prospective Study to Compare Safety and Efficacy of Various Anti-Glaucoma Agents and Evaluate the Effect of Aerobic Exercise on Intra-Ocular Pressure in Newly Diagnosed Primary Open Angle Glaucoma Patients in a Tertiary Care Hospital. Four cases of patients with aortic incompetence secondary to rheumatoid arthritis are presented. The purpose of this study was to compare the caries-preventive methods used for children and adolescents in these four countries. An activin A/inhibin B ratio of less than 1 and very high inhibin B levels correlated with large numbers of oocytes, while a ratio of 1-2 and high inhibin levels correlated with regular numbers of oocytes. In this manuscript, we describe the distribution of FMRFamide immunoreactive materials in the Drosophila central nervous system and gut, and correlate it with the expression of specific FaRPs and their activities. The present meta-analysis included all published relevant randomized controlled trials (RCTs) and aimed to compare the safety and efficacy of TAVI compared to surgical aortic valve replacement (AVR). In multicellular organisms the development of adhesion bonds, either among cells or among cells and components of the extracellular matrix, is a crucial process. Fifty percent of parents surveyed had spoken to their daughter about their possible infertility. The comprehensive aortic root and valve reconstruction (CARVAR) technique comprises two main procedures, which are aortic root reduction using prosthetic rings and neo-leaflet reconstruction using a pericardial patch xanax medication . We report the echocardiographic findings in a patient with severe pulmonary hypertension, before and after the inhalation of aerosolized iloprost.

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To test this, weaned mice were orally inoculated by gavage with either an E. Most of them, however, focused on robustness against a single node mutation. Our is zyrtec safe when breastfeeding study shows that QSRL treatment of primary melanocytes in vitro does not cause major alterations of global gene expression and particularly of genes associated with malignant melanoma. MI-219 activates p53 in normal tissues with minimal p53 accumulation and is not toxic to animals. Activity diaries were completed contemporaneously to record episodes of infant handling. In a previous study (5), the constructed phylogenetic tree for leptospires belonging to 12 different serovars common in Central Europe made the prediction of serovar from knowing the genotype and vice versa possible. HORIZONTAL RIDGE AS A POSTERIOR POLE FINDING IN A HIGHLY MYOPIC EYE WITH DOME-SHAPED MACULA.

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