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Azitrix

Azitrix belongs to a group of Macrolide Antibiotics useful for treating numerous infections caused by bacteria like middle ear infections, traveler's diarrhea. Along with other medications, it is sometimes used for malaria. It is also used to treat a number of intestinal infections and sexually transmitted infections including gonorrhea and chlamydia. Administration of the medicine takes place either by mouth or intravenously with doses once per day.

Other names for this medication:
Altezym, Amovin, Amsati, Azatril, Azicu, Azifast, Azimac, Azimakrol, Azimit, Azinil, Azinom, Azithrocin, Azitro, Azitrom, Azyter, Bactexina, Clearsing, Doyle, Ezith, Goldamycin, Hemomycin, Kromicin, Magnabiotic, Neofarmiz, Tromic, Vectocilina, Zemycin, Zertalin, Zibac, Zithromac, Zitrocin, Zival

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Also known as: Azithromycin

Description

Azitrix (Azitrix tablets and Azitrix for oral suspension) contain the active ingredient azithromycin, a macrolide antibacterial drug, for oral administration. Azitrix has the chemical name (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[(2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl) oxy]-2-ethyl-3,4,10-trihydroxy-3,5,6,8,10,12,14-heptamethyl-11-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-1-oxa-6-azacyclopentadecan-15-one. Azitrix is derived from erythromycin; however, it differs chemically from erythromycin in that a methyl-substituted nitrogen atom is incorporated into the lactone ring. Its molecular formula is C38H72N2O12, and its molecular weight is 749.00.

Azitrix, as the dihydrate, is a white crystalline powder with a molecular formula of C38H72N2O12∙2H2O and a molecular weight of 785.0.

Azitrix is supplied as tablets containing azithromycin dihydrate equivalent to either 250 mg or 500 mg azithromycin and the following inactive ingredients: dibasic calcium phosphate anhydrous, pregelatinized starch, sodium croscarmellose, magnesium stearate, sodium lauryl sulfate, hypromellose, lactose, titanium dioxide, triacetin, and D&C Red #30 aluminum lake.

Azitrix for oral suspension is supplied in bottles containing azithromycin dihydrate powder equivalent to 300 mg, 600 mg, 900 mg, or 1200 mg azithromycin per bottle and the following inactive ingredients: sucrose; sodium phosphate, tribasic, anhydrous; hydroxypropyl cellulose; xanthan gum; FD&C Red #40; and spray dried artificial cherry, creme de vanilla, and banana flavors. After constitution, each 5 mL of suspension contains 100 mg or 200 mg of azithromycin.

Dosage

Take Azitrix 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.

Azitrix 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. Azitrix 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 Azitrix dosage information

Overdose

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

Storage

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 Azitrix 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. Azitrix can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

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In particular, the long-distance effects of insertional mutagenesis bring into question the relevance of the lists of disease-associated retroviral integration targets, which did not undergo functional validation. Its use was recently reported as a sclerosing agent for percutaneous treatment of lymphoceles following renal transplantation. BIS decreased to 0 for approximately 15 min, indicating that lidocaine and sevoflurane interact to decrease BIS. Surgical treatment of spontaneous or traumatic intracerebral hemorrhages. Thus, insomniacs have increased beta and decreased alpha activity relative to normals prior to the onset of stage 2 sleep. No severe adverse events were related to the vaccine, and no difference in terms of tolerability was observed between the sites of vaccination or between the levaquin antibiotic category vaccine formulations. We targeted Harlem, NY (using the South Bronx for comparison), and disseminated informational material at community forums, pharmacist training programs, and counseling or outreach programs for IDUs. Lung transplantation in the management of patients with lymphangioleiomyomatosis: baseline data from the NHLBI LAM Registry. Students were able to opt out of the session by contacting the course organisers. Subcutaneous injection of PK 10169 was not followed by an increase of the thrombin time.

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Here we report that dentin matrix protein 1 (DMP1), an acidic protein, can nucleate the formation of hydroxyapatite in vitro in a multistep process that begins by DMP1 binding calcium ions and initiating mineral deposition. Factor VIII activity (Factor VIII: C) was determined in a total of 165 donors of plasmapheresis. Current classification criteria for SJIA may not be particularly sensitive for diagnosis at presentation. 33-item electronic survey containing 9 questions evaluating knowledge, 16 questions assessing attitudes, and 8 questions requesting demographic information. Classification as a mature teratoma carries with it a follow-up regimen that includes numerous radiological investigations with their attendant radiation exposure. Before one changes well-established habits of practice it is necessary to evaluate non-commercial sources of data.

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Strepsiptera evolved two strictly different types of tarsal attachment structures: hairy surfaces in the males and smooth flexible pads in the first instar larvae. The fiber-dissection technique provides unique 3-dimensional anatomic knowledge of the white matter. The increased burden of cardiovascular disease in chronic kidney disease cannot be explained by traditional risk factors alone. We also propose simple t-like statistics for testing changes in (i) the mean (presence of an event-related potential), (ii) the amplitude variance (presence of (de)synchronization) and (iii) the concentration of phases (phase locking). A method of simultaneous quantification of neurosteroids by gas chromatography-mass spectrometry (GC-MS) had been established. The general scientific concensus is that, although the interaction could be somewhere between linear and supramultiplicative, it is likely a combination, and closer to multiplicative.

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Assuming that non-HDL-C levels are raised in IHD, a cross sectional study was designed to evaluate the levels of non-HDL-C in patients of IHD. Consistent with the PCR array results, EphB2 levels of mRNA and protein were reduced in IL after fear extinction compared with fear conditioning, suggesting that EphB2 signaling in IL regulates fear extinction memory in adolescents. Metabolism of glucagon-like peptide-2 in pigs: role of dipeptidyl peptidase IV. Influence of interfacial potential on friction and surface damage. The log of the octanol/water partition coefficient (log P) was 1.01 for apocynin and 1.82 for diapocynin. Different hue coding ramipril type of drug underlying figure segregation and region detection tasks.

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