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Azidraw (Azithromycin)

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Azidraw is used for Bacterial infections and other conditions. Azidraw may also be used for purposes not listed in this medication guide. Azidraw contains Azithromycin as an active ingredient. Azidraw works by stopping the growth of bacteria.

Other names for this medication:
Amsati, Azalid, Azatril, Azenil, Azibiot, Azimac, Azithral, Azithrex, Azitrocin, Azitrovid, Azomac, Azrolid, Azyter, Bezanin, Clearsing, Doromax, Doyle, Goldamycin, Inedol, Misultina, Momicine, Neofarmiz, Respazit, Rozith, Simpli, Tanezox, Tridosil, Tromix, Trozocina, Unizitro, Vinzam, Zemycin, Zentavion, Zifin, Zithromac, Zithromycin, Zitrolid

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Also known as: Azithromycin


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

Azidraw 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.

Azidraw 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.

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.


This section provides information on the proper use of a number of products that contain azithromycin. It may not be specific to Azidraw 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 Azidraw® oral liquid or tablets with or without food.

Shake well the bottle of Azidraw® 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 Azidraw®. 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.


Adverse reactions experienced at higher than recommended doses were similar to those seen at normal doses particularly nausea, diarrhea, and vomiting. In the event of overdosage, general symptomatic and supportive measures are indicated as required.


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 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.


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.

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Gonadotrophin-induced desensitization of the luteal adenylyl cyclase throughout pregnancy and pseudopregnancy in the rabbit and the rat. Current perspectives for AT(1)-receptor blockers in the management of heart failure. A partitioned likelihood analysis of swallowtail butterfly phylogeny (Lepidoptera:Papilionidae). Joint blind restoration and surface recovery in photometric stereo. Initial characterization of the DNA polymerase product by gel electrophoresis showed a single DNase I sensitive band, migrating slightly mellaril dosage faster than the woodchuck hepatitis virus DNA polymerase product. The purpose of this study is to demonstrate the benefit of the bone-anchored hearing aid (BAHA) in a group of patients with unilateral conductive or mixed hearing loss. Release of the known toxic material, TDA, is consistent with these observations and strongly suggests that an alternative material be used in this application. The effect of the concentration of the reagents on the rate of the reaction was investigated and a kinetic method for determination of the compounds is proposed.

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p53 is essential for the cellular responses to DNA damage that help to maintain genomic stability. Patients underwent treatment on a clinical trial using a 60-min hyperthermic isolated hepatic perfusion (IHP) with melphalan. Melting point depression, that is, the depression of solid-nematic transition temperature observed max dose of glucotrol from the pores as compared with that in bulk LC, is seen to be very sensitive to the pore size, and it can be used for the determination of pore size of an unknown material. Abdominal rectopexy, the standard surgical approach, has significant attendant risk and does not address any concomitant rectocele. Radiographic measurements were made from standardised digital AP pelvic radiographs. The expected spontaneous peaking was seen only after stopping the drug. The tensile strength, stress, relaxation and creep of the four meshes were different. These results indicated that the expression amount of p21(WAF1) in 2BS cells was negatively related with its susceptibility to apoptosis induced by NaBu. All were administered a complete battery of neuropsychological tests and the Minnesota Multiphasic Personality Inventory.

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The single-chain variable acticin fragment (scFv) was constructed and expressed in Escherichia coli as a soluble protein and at the surface of the filamentous M13 phage and was compared with the full-length antibody (Ab). On the other hand, follow-up examination by means of the ankle pressure measurement was useful to detect new occurrences of stenotic lesions in the postoperative period. Removing the health domain from the Index of Multiple Deprivation 2004-effect on measured inequalities in census measure of health. A double-blind test with oxazepam confirms the value of this new vehicle. Becoming familiar with different research study designs helps one to understand and interpret the results of clinical trials.

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The nuclear matrices from the prostates collected at these time points were then isolated and the NMPs were characterized by high-resolution two-dimensional gel electrophoresis. Rates of 4-nitrophenol and formaldehyde production from the O-demethylation of 1-methoxy-4-nitrobenzene by P450 1A2 isolated from rabbit liver produced biphasic plots, when plotted against substrate concentration. Operative results were consistent with the morbidity and mortality figures from large reviews. I have presented two complementary lines of speculation in this article. cipro suspension coupon Excitation and inhibition of highly excitable reflex curves in chronically denervated albino rats. The problem of subpixel unmixing is a prominent issue in the quantitative application of remote sensing. It catalyzes the conversion of 3-hydroxybenzoate to 3,4-dihydroxybenzoate with concomitant requirements for equimolar amounts of NADPH and molecular oxygen. A total of 342 eyes of 342 patients (207 women and 135 men) with ARMD and subfoveal CNV were treated with at least two PDT. Computed tomography (CT) and cranial magnetic resonance imaging (MRI) are performed and demonstrate a left basal ganglia tumour (nucleus lentiformis). In an effort to evaluate the occurrence of selected enteric organisms with zoonotic and biohazard potential in a research colony setting, we performed a prevalence study examining 61 juvenile and young adult rhesus macaques participating in a transplant immunology project.

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Determinants for stop-transfer and post-import pathways for protein targeting to the chloroplast inner envelope membrane. We isolated a protein, from a cell line of human origin, which exhibits extensive differentiation inducing activity toward Friend leukemia cells. In the urogenital system, mPGES-2 was highly expressed in the renal cortex, followed by the renal medulla and ovary, with lower levels in the ureter, bladder and uterus. Rat complement factor H: molecular cloning, sequencing and quantification with a newly established ELISA. Of 197 sibships that were evaluated 47.6 per cent, excluding the probands, had undiagnosed uropathology. We measure an activation energy for the diffusion of incorporated Pd atoms of 0.88 eV, which is in good agreement with our ab initio calculated energy of 0.94 eV. Anesthesia was accomplished with intravenous thiamylal and Innovar. The present study is designed to evaluate the protective effects of SIRT1 on endothelial senescence and to elucidate the underlying mechanisms. Deferred standards, an on-line qualification, validation and system stability probe for chromatographic assay. We present a clinical case and provide suggestions for diagnosis and treatment of this unusual pathology.

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