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Azidraw (Azithromycin)
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Azidraw

Azalides are a class of macrolide antibiotics which contain a nitrogen in the macrolide ring. This imparts different pharmacokinetic properties and is associated with greater stability of the molecule. One such Azalide is the antibiotic Azidraw. This medication is a macrolide antibiotic used for various bacterial infections such as infections of the middle ear, throat, bronchus, sinuses, skin and soft tissue. It is also useful in treating pneumonia, typhoid, gonorrhoea, granuloma inguinale and chancroid. It prevents bacterial growth.

Other names for this medication:
Altezym, Azalid, Azicid, Azicu, Azifast, Azihexal, Azimycin, Azinom, Azithin, Azithrex, Azithro, Azithrox, Azitrin, Azomac, Azromax, Binozyt, Clearsing, Ezith, Fabramicina, Faxin, Goldamycin, Ilozin, Koptin, Magnabiotic, Misultina, Naxocina, Novozitron, Ordipha, Penalox, Ricilina, Sumamed, Toraseptol, Ultrabac, Zimax, Zinfect, Zithrocin, Zithrogen, Zomax

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Imuran, Suprax, Lopid, Precose, Glucotrol, Pyridium

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Also known as: Azithromycin

Description

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

Azidraw is the local analog (generic) of more famous drug Azidraw that has the same active substance (ingredient) and in result the same therapeutic effect. The main difference is that Azidraw 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 Azidraw only in the pharmacies of the country where it is produced. With us, you can buy its more famous analog Azidraw, 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

Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label. The dose and length of treatment with Azidraw may not be the same for every type of infection.

You may take most forms of Azidraw with or without food.

Take Azidraw extended release liquid (oral suspension) on an empty stomach, at least 1 hour before or 2 hours after a meal.

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. Do not save for later use. To make sure you get the entire dose, add a little more water to the same glass, swirl gently and drink right away.

Throw away any mixed Azidraw oral suspension that has not been used within 12 hours.

Shake the oral suspension well just before you measure a dose. Measure the liquid with a special dose-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 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. Azithromycin will not treat a viral infection such as the common cold or flu.

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

Overdose

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

Storage

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.

Side effects

The most common side effects associated with Azidraw 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

Do not take antacids that contain aluminum or magnesium within 2 hours before or after you take azithromycin. This includes Acid Gone, Aldroxicon, Alternagel, Di-Gel, Gaviscon, Gelusil, Genaton, Maalox, Maldroxal, Milk of Magnesia, Mintox, Mylagen, Mylanta, Pepcid Complete, Rolaids, Rulox, and others. These antacids can make azithromycin less effective when taken at the same time.

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, stop taking azithromycin and call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to.

Avoid exposure to sunlight or tanning beds. Azidraw can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

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Polymer-supported bisBINOL ligands for the immobilization of multicomponent asymmetric catalysts. We herein report a case of ectopic prostatic tissue in the retrotrigone of the bladder. Phase I trials have also been conducted on the basis of preclinical studies that demonstrated promising antitumor activity with acceptable safety results in human B-cell lymphoma models. The continuous assay for the assessment of TF PCA on intact cells is applicable for high-throughput screening to allow for the determination of compounds that modulate TF PCA. Mutation detection may also be important for patient management and identification of affected family members.

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However, controversy persists regarding the optimal ventilator settings for patients without ARDS receiving mechanical ventilation. The purpose of this article is therefore to review the basics of programmed cell death. Effects of chronic morphine administration on pregnant rats and their offspring. Finally, pretreatment with ERK-specific inhibitor PD98059 reversed decursin-induced p21WAF1 expression and decursin-inhibited cell growth. Overdrainage of inderal dosage iv the cerebrospinal fluid (CSF) was performed for brain retraction during the operation in all four cases.

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However, its value in confirming a diagnosis of presumptive endometriosis has not been extensively studied. Case ascertainment was evaluated through the capture-recapture method. The purpose of the study was to investigate the total and bio-available contents of heavy metals (Cd, Co, Ni, and Pb) and to determine their spatial variability in the Amik Plain, Turkey. The harmonic vibrational frequencies, infrared intensities and Raman scattering activities of flurbiprofen were calculated by density functional B3LYP methods by using 6-31G(d,p) basis set. Experiments were performed on cells isolated from venous blood obtained from healthy donors. Therefore, it is expected to be a reasonable alternative in cases where there is no PLL.

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Saturated and mono-unsaturated fatty acid biosynthesis in brain: relation to development in normal and dysmyelinating mutant mice. Striving for balance in daily life: experiences of Swedish women and men shortly after a myocardial infarction. Although there was a significant reduction in meal frequency and the number of meals taken outside the family, a significant increase in body weight was noted during Ramadan. Furthermore, these issues should be considered in a holistic manner. Patterns of discrete DNA damage streaks across nuclei or saturated nuclear damage were observed, with saturated nuclear damage being more predominant as samples were positioned closer to the physical Bragg peak. In summary, ERK1/2 activation occurred early in neurons after HI in the neonatal brain, and mainly in cells displaying signs albenza cost of damage. Incomplete pulmonary sequestration: difficulty of angiographic differential diagnosis. Another entity that may occur independently or concurrently in critically ill patients is a myopathy, giving rise to difficulties in distinguishing between them. Dose-response relationships for phenylisopropyladenosine (PIA) were determined for hearts adrenergically stimulated by isoproterenol.

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