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Azomex (Azithromycin)

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Azomex is an antibiotic. It's widely used to treat chest infections such as pneumonia, infections of the nose and throat such as sinus infection (sinusitis), skin infections, Lyme disease, and some sexually transmitted infections.

Other names for this medication:
Atizor, Azicid, Azicine, Azimax, Azithin, Azithrex, Azithromycin, Azithrox, Azithrus, Azitrim, Azitro, Azitrotek, Aziwok, Azomac, Azomax, Cinalid, Doyle, Hemomycin, Imbys, Inedol, Misultina, Neozith, Novatrex, Novozithron, Oranex, Penalox, Ricilina, Rozith, Simpli, Sitrox, Talcilina, Tanezox, Tridosil, Tromix, Zibramax, Zithrin, Zithrocin, Zithromycin, Zitrex, Zitrim, Zitrocin, Zitrofar, Zitroken, Zitrotek, Zocin, Zomax

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Also known as: Azithromycin


Azomex is used to treat many different types of infections caused by bacteria, such as respiratory infections, skin infections, ear infections, and sexually transmitted diseases. In children, it is used to treat middle ear infection, pneumonia, tonsillitis, and strep throat.

Azomex, a semisynthetic antibiotic belonging to the macrolide subgroup of azalides, is used to treat STDs due to chlamydia and gonorrhea, community-acquired pneumonia, pelvic inflammatory disease, pediatric otitis media and pharyngitis, and Mycobacterium avium complex (MAC) in patients with advanced HIV disease. Similar in structure to erythromycin. azithromycin reaches higher intracellular concentrations than erythromycin, increasing its efficacy and duration of action.

Bioavailability is 37% following oral administration. Absorption is not affected by food. Azithromycin is extensively distributed in tissues with tissue concentrations reaching up to 50 times greater than plasma concentrations. Drug becomes concentrated within macrophages and polymorphonucleocytes giving it good activity against Chlamydia trachomatis.


Use Azomex as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Azomex is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using Azomex at home, a health care provider will teach you how to use it. Be sure you understand how to use Azomex. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

Do not use Azomex if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

o clear up your infection completely, use Azomex for the full course of treatment. Keep using it even if you feel better in a few days.

Ask your health care provider any questions you may have about how to use Azomex.


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


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

Side effects

The most common side effects associated with Azomex 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.


Do not take antacids that contain aluminum or magnesium within 2 hours of taking Azomex.

Before taking Azomex, tell your doctor if you are using any of the following drugs: nelfinavir (Viracept); digoxin (Lanoxin, Lanoxicaps); ergot medicine such as methysergide (Sansert), ergotamine (Ergostat, Medihaler, Cafergot, Ercaf, Wigraine), dihydroergotamine mesylate (D.H.E., Migranal Nasal Spray); triazolam (Halcion); carbamazepine (Carbatrol, Tegretol); cyclosporine (Neoral, Sandimmune); phenytoin (Dilantin); cholesterol-lowering medicines such as lovastatin (Mevacor), atorvastatin (Lipitor), or cerivastatin (Baycol); a calcium channel blocker such as diltiazem (Cartia XT, Diltiazem, Tiazac), felodipine (Plendil), nicardipine (Cardene), nifedipine (Procardia, Adalat), nimodipine (Nimotop), verapamil (Calan, Covera-HS); HIV medicines such as indinavir (Crixivan), ritonavir (Norvir), saquinavir (Invirase); alprazolam (Xanax), diazepam (Valium), midazolam (Versed), triazolam (Halcion); theophylline (Theo-Dur, Theolair, Theochron); warfarin (Coumadin); pimozide (Orap); or another antibiotic, especially clarithromycin (Biaxin) or erythromycin (E-Mycin, E.E.S, Ery-Tab).

If you are using any of these drugs, you may not be able to use Azomex, or you may need dosage adjustments or special tests during treatment.

There are many other medicines that can interact with Azomex. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors.

Do not start using a new medication without telling your doctor. Keep a list with you of all the medicines you use and show this list to any doctor or other healthcare provider who treats you.

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The desensitizing effect of the 530 nm background on UV-pigment driven responses provides new evidence in support of the hypothesis of functional co-expression of the M-pigment in cones expressing primarily the UV-pigment. Although they are asymptomatic early in life, their identification and successful treatment in adolescence can establish management regimens and habits that protect and extend life. AMI patients have a greater risk of new-onset diabetes when compared to non AMI patients, especially those with mild metabolic abnormalities. There was no significant impact on parental mental health (General Health Questionnaire) scores. physico-chemical characteristics of the residues responsible for selective binding. Plasma membrane specialization at the discharge site of the excretory poreless vacuole of the ciliate Euplotes raikovi. Two cases with expanding pituitary tumours following treatment with 2-bromo-alpha-ergocryptine are presented. No episode of paradoxical air embolism was observed in the 90 remaining patients, although 16 cases of pulmonary air embolism were detected during surgery. Three of the 19 family members studied were found to have a deficiency of both factors V and VIII.

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Hand-held model of a sarcomere to illustrate the sliding filament mechanism in muscle contraction. Percutaneous transluminal coronary angioplasty (PTCA) was performed on 200 patients and failed in 36, 12 of whom underwent myocardial revascularization within 3 hours after the angioplasty attempt. We develop a statistical model that illustrates under which assumptions thresholding is optimal in the analysis of such microarray data. Annual review of the knowledge in 49 diabetic children (aged 8-14, mean 12 years) who are regular clinic attenders demonstrated poor theoretical and practical skills that were irrespective of the duration of diabetes. Transient non-native interactions in early folding intermediates do not influence the folding kinetics of Escherichia coli tryptophan synthase beta 2 subunits. Students also quantify the results, evaluate who the intended audience is and how they most appropriately target them, and determine if there are other management problems that could be addressed with the science. In vitro and in vivo studies implicate the kidney as an important site for clearance and subsequent degradation of atrial natriuretic factor. The placenta was classically considered a barrier, but in 1957 this notion was shattered. Although SPHK1 has gained increasing prominence as an important enzyme in cancer biology, its potential as a predictive biomarker and a therapeutic target in cervical cancer remains unknown.

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Inhibition of adenosine deaminase and purine nucleoside phosphorylase and T-cell function in germfree mice and human peripheral blood. Tinea faciale mimicking seborrheic dermatitis in a patient with AIDS. Interactions of nanoparticles with lipid vesicles: a population based computer aided image analysis approach. 3 degrees C 30 min after an injection of 0.3 mg/kg of 8-OH-DPAT. cDNA was synthesized from total RNA extracted from DCT microdissected from collagenase-treated kidneys. Reduced power and phase locking of the early auditory gamma-band response (EAGBR) have been reported in schizophrenia, but findings are equivocal. Status of tobacco prevention practices in ambulatory and hospital care. No adequate preventative measures exist in practice, beyond the avoidance of risk factors.

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Health promoting behaviors of urban African American female heads of household. Relative hydrophobicity of surfaces of erythrocytes from different species as measured by partition in aqueous two-polymer phase systems. The dose-response relation observed between cumulative exposure to respirable crystalline silica and lung cancer mortality among workers without radiological silicosis suggests that silicosis is not a necessary co-condition for silica related lung carcinogenesis. Implementing federal transition initiatives for youths with severe handicaps: the Utah Community-Based Transition Project. Small-scale batch studies were performed to study the influence of the initial enzyme and alcohol concentrations, and the substrates molar ratio. Use of small interfering ribonucleic acids to inhibit the adipogenic effect of alcohol on human bone marrow-derived mesenchymal cells. Although different tissues appear to contain the same tRNA methyltransferases, the patterns of methylated nucleosides are different.

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Elevation of myostatin and FOXOs in prolonged muscular impairment induced by eccentric contractions in rat medial gastrocnemius muscle. The inhibitory receptive field was located in the molar and/or second premolar alveolar gingivae. Effects of sensory denervation and deprivation on a single cortical vibrissal column studied with 2-deoxyglucose. Iodine deficiency (ID) during development results in dysfunction of the central nervous what other drug is like tetracycline system (CNS) and affects psychomotor and motor function. The agonist-antagonist hybrid proposed in this study not only enhances our understanding of the possible structural requirements and rational design of receptor partial agonists, but it also enhances our understanding of the possible molecular basis of receptor partial activation. It is capable of estimating the deterministic component of the signal and removes the noise uncorrelated with stimulus even if this noise is colored and without the need for prealignment. Characterization of vasopressin-responsive collecting duct adenylyl cyclases in the mouse. Extension to Western Africa of Plasmodium falciparum resistance to chloroquine.

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