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Azitrix (Azithromycin)

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Azitrix is created by pharmacy specialists to struggle against dangerous infections (STD, pneumonia, bronchitis, lungs, throat or ears infections, skin infections, MAC). Target of Generic Azitrix is to control, ward off and terminate bacteria.

Other names for this medication:
Amsati, Azadose, Azicu, Azilide, Azimakrol, Azimax, Azimit, Azinix, Azinom, Azirox, Azithral, Azithrocin, Azithrox, Azithrus, Azitrom, Azitromicina, Azitrovid, Azitrox, Azomax, Azomex, Azomycin, Clearsing, Imbys, Maczith, Naxocina, Novozithron, Novozitron, Opeazitro, Orobiotic, Rarpezit, Respazit, Rozith, Texis, Tromix, Zaret, Zedd, Zertalin, Zimax, Zinfect, Zirocin, Zithrin, Zithrogen, Zitrim, Zymycin

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Also known as: Azithromycin


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

Azitrix 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.

Azitrix 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.

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


It is important that your child completes the course of antibiotic. This means that they must take the medicine for the number of days that the doctor has told you to, or until all the medicine has been taken. If you stop giving the antibiotic too soon, the troublesome bacteria that are left will start to multiply again, and may cause another infection. There is also a risk that these bacteria will be resistant to (no longer be killed by) the first antibiotic. This means that it might not work next time, and your child might need a different antibiotic, which might not work as well or cause more side-effects.

Children are sometimes sick (vomit) or get diarrhoea when taking antibiotics. Encourage them to drink water to replace the fluid they have lost. If it is severe or your child is drowsy, contact your doctor.

Do not give your child any medicine to stop the diarrhoea unless your doctor has told you to, as this can make things worse.

Try to give the medicine at about the same times each day, to help you remember, and to make sure that there is the right amount of medicine in your child’s body to kill the bacteria.

Only give this medicine to your child for their current infection.

Never save medicine for future illnesses. Give old or unused antibiotics to your pharmacist to dispose of.

Only give the antibiotic to the child for whom it was prescribed. Never give it to anyone else, even if their condition appears to be the same, as this could do harm.


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


Keep the medicine in a cupboard, away from heat and direct sunlight.

You may need to keep liquid medicine in the fridge – check the instructions on the bottle. Make sure that the medicine doesn’t freeze.

Make sure that children cannot see or reach the medicine.

Keep the medicine in the container it came in.

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.


Hypersensitivity to Azitrix and other macrolide antibiotics.

Azitrix crosses the placental barrier. Use in pregnancy only in cases where the intended benefits to the mother outweighs the potential risk to the fetus.

If necessary to use Azitrix in the lactation period should solve the issue of termination of breastfeeding.

Azitrix not recommended for use in patients with compromised liver function.

Azitrix uses with careful with impaired renal function.

This medication should be taken at least 1 hour before or 2 hours after eating or taking of antacids.

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Combined magnetic resonance imaging and spectroscopy in experimental regional injury of the brain. Coronavirus and parainfluenza virus were detected in one patient each, and Epstein-Barr viruses were detected in three patients. Multiple amyloidomas in an HIV patient presented as inguinal and mediastinal masses: a case report diagnosed by fine-needle aspiration. Certain spoil groups showed high potential salinity by releasing high sodium and chloride concentrations. The inhibitor bound in the active site has different conformations in the two orientations. Cross-match-to-transfusion ratios (C:T) were calculated and compared to current trust and the British Society of Haematology (BSH) guidelines. The respiratory and cardiovascular response to immersion in cold and warm water. Of interest, LRRC10 exhibits dynamic intracellular expression patterns in cardiomyocytes. Implications for Rehabilitation HIV, its co-morbidities and treatments cause health conditions and impairments that have the potential to develop into disability. These, together with a previously described technique, were applied to mapping binding sites on plasmid DNAs containing either the human zeta-globin or chicken beta-globin gene promoters.

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Reliability and validity of a treatment fidelity assessment for motivational interviewing targeting sexual risk behaviors in people living with HIV/AIDS. Robotic assisted laparoscopic radical cystoprostatectomy: operative and pathological outcomes. to the common antifungal agents in a German university hospital. Single-twitch tension, peak tetanic force generation, and fatigue rate were determined at optimal preload. Targeting therapeutics to an exposed and conserved binding element of the HIV-1 fusion protein. In this before-and-after trial, 17 nonambulatory patients with chronic hemiparetic stroke were recruited. Externalizing behavior problems among polydrug cocaine-exposed children: Indirect pathways via maternal harshness and self-regulation in early childhood. In order to be able to distinguish between proliferation inhibition, apoptosis, necrosis and recovery of proliferation, we performed TUNEL assays and fluorescence analysis cell-counter (FAC) analysis. Training effect was measured by maximal oxygen uptake (Vo(2)max) anaerobic threshold (Vo(2AT)), and the corresponding work rates (WR) (in watts)-WRmax and WR(AT)-before and after 10 weeks of training. On a background of progressively rising BP and parallel increasing R, ECG changes were recorded.

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To evaluate the efficacy of a biodegradable silage coating for the ability to protect timothy (Phleum pratensa) type silage against spoilage and its quality under natural conditions. The adverse effects of anticancer agents are a is biaxin an antibiotic limiting factor for cancer chemotherapy, therefore, liposomal formulations have the potential to improve the therapeutic efficacy of anticancer agents by enhancing their accumulation in tumors and reducing non-selective distribution to normal tissues, which is known as the enhanced permeability and retention effect. A 53-year-old postmenopausal woman was transferred to our emergency department for drowsiness, hypotension, and lower abdominal discomfort. The animal was rewarded with a drop of sucrose solution whenever the muscle activity exceeded a defined reward threshold. Liver peroxisomes were found to be functionally defective when purified after infection. The authorship indexes for REDAR are similar to those of other Spanish publications, although the institutional rate is lower. Tissue IL-1ra expression and serum IL-1ra level were examined by enzyme-linked immunosorbent assay (ELISA), Western blotting, and immunohistochemistry in normal controls and patients with cervical carcinoma. No answer in the images: ultrasound, computed tomography, and magnetic resonance imaging suggested 3 possible diagnoses, none of which were accurate. Preoperatively, 0.5-1 ml study medication was administered, followed by increments of 0.2-0.5 ml during surgery guided by heart rate and systolic blood pressure. Source apportionment of ambient volatile organic compounds in Beijing.

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Preventive effect of endothelin-1 pretreatment on hypoxia-induced injury in cultured neonatal rat cardiomyocytes. Quantification of hepatitis B surface antigen and E antigen: correlation between Elecsys and architect assays. Using these techniques, a gas chromatography/mass spectrometry method was developed to determine that in the biosynthesis of tetrahydrobiopterin de novo, in preparations of bovine adrenal medulla, the C-6 proton of tetrahydrobiopterin is derived from water and not from NADPH. Combining age and HBsAg level predicts post-treatment durability of nucleos(t)ide analogue-induced HBeAg seroconversion. Secondly, the T cells are excluded from the multicellular aggregates formed by agglutination of the remaining cells with wheat germ lectin. Novel surface haptic devices, however, have the potential to provide displays to multiple fingertips simultaneously, affording the possibility of parallel search.

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PBLs bearing LFA-1Af can enhance COLO526 adhesion to both resting and activated HUVECs. Our data indicate that FLG mutations in Japan are unique from those found in European-origin populations. Stress-inducible expression of At DREB1A in transgenic peanut (Arachis hypogaea L.) increases transpiration efficiency under water-limiting conditions. Findings suggest that it is indeed possible to benefit from both effortful and minimal cognitive processing strategies and that they should be used complementarily. Treatment strategy of refractory depression and its presynaptic mechanism of action. thanks the Croucher Foundation of Hong Kong for financial support.

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