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Aziphar (Azithromycin)
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Aziphar

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

Other names for this medication:
Azicine, Azigram, Azimac, Azinil, Azinix, Azinom, Azithromycin, Azitrocin, Azitrox, Azrolid, Aztrin, Azycyna, Azyter, Goxil, Imbys, Macrozit, Neozith, Novozitron, Opeazitro, Oranex, Penalox, Pretir, Ribotrex, Tritab, Tromix, Trozocina, Ultreon, Vectocilina, Zaret, Zistic, Zitrex, Zitroken, Zitrolid, Zycin, Zymycin

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Omnicef, Avelox, Biaxin, Zithromax, Keflex, Flagyl

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Also known as: Azithromycin

Description

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

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

Dosage of Aziphar is setted individually according to nosology, disease severity and sensitivity of the pathogen. Dosage for adults for oral administration is 0.25-1 g 1 time/day; for children - 5-10 mg/kg 1 time/day. The duration of administration is 2-5 days.

Overdose

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

Storage

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 Aziphar 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

Ketolide allergy. History of cholestatic jaundice/hepatic dysfunction associated with prior use.

Pneumonia: oral treatment is for mild, community-acquired cases suitable for outpatient therapy only. Discontinue if signs/symptoms of hepatitis occur. Known QT prolongation, proarrhythmic conditions, clinically significant bradycardia: avoid. Allergic symptoms may recur after initial successful symptomatic treatment. Myasthenia gravis. Hepatic or renal impairment. Elderly. Pregnancy (Cat.B). Nursing mothers.

Avoid concomitant aluminum- or magnesium-containing antacids. Monitor with digoxin, phenytoin, warfarin. Monitor for azithromycin toxicity (eg, liver dysfunction, ototoxicity) with nelfinavir. Concomitant Class 1A (eg, quinidine, procainamide), or Class III (eg, dofetilide, amiodarone, sotalol) antiarrhythmics, or others known to prolong the QT interval: avoid.

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Clinical parameters were compared between responders to the therapy (increase in platelet count) and nonresponders, as well as between H pylori-positive and -negative patients. Effect of virus-induced destruction of villous epithelium on intestinal secretion induced by heat-stable Escherichia coli enterotoxins and prostaglandin E1 in swine. This method has been utilized in six patients, and there has been no recurrence of the defect or evidence of a lumbar hernia. 13 ASA physical status I and II patients undergoing lower abdominal or lower extremity surgery. To evaluate the effect of urethral dilatation (UD) on urgency symptoms in women with overactive bladder (OAB) and voiding dysfunction. A case of the new overgrowth syndrome--macrocephaly with cutis marmorata noroxin medication , haemangioma and syndactyly. Positron emission tomography study of a chronic pain patient successfully treated with somatosensory thalamic stimulation. Administration of estradiol to neonatal WT or ArKO mice increased dendritic growth, spinogenesis, and synaptogenesis in the Purkinje cell.

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Health reform and consequent reorganizations were seen to reduce the ability of some services to undertake health promotion. Information is provided concerning this polluted habitat and seasonal distribution of the zoosporic fungi. The aim of this study was to compare estimates of the maximum bladder capacity (MBC) using cystometry, uroflowmetry, and a 24-h voiding diary in women with urinary incontinence. Moreover, the response was almost completely inhibited by tetrodotoxin and N(G)-nitro-L-arginine, but only moderately inhibited by atropine and indomethacin. A retrospective study was conducted to identify patients hospitalised at home between 2001 and 2005. Site-directed spin labeling (SDSL) combined with electron paramagnetic resonance (EPR) spectroscopy has emerged as a powerful approach to study structure and dynamics in proteins. These differences result partly from technical differences in the algorithms for the determination of bone mineral content and bone area and partly from the use of different manufacturer-derived reference databases. Probable poststreptococcal anterior uveitis in a 3-year-old boy.

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Cloned dddD from the marine bacterium Marinomonas and from two bacterial strains that associate with higher plants, the N(2)-fixing symbiont Rhizobium NGR234 and the root-colonizing Burkholderia cepacia AMMD, conferred to Escherichia coli the ability to make DMS from DMSP. Some studies on the experimental infection of golden hamsters with Taenia solium. The lesions were then evaluated both qualitatively and quantitatively. The development and evaluation of alternative communication strategies what happens when you take flagyl and drink alcohol to facilitate interactions with Somali refugees in primary care: a preliminary study. The interest in basic angiogenesis research is sparked by the translational therapeutic potential aimed at developing anti-angiogenesis as a novel therapeutic modality for tumours and a number of non-oncological diseases, such as rheumatoid arthritis, psoriasis, diabetic retinopathy and age-dependent macula degeneration.

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Origin of inhibitors of the influenza virus in normal human serum. The amount of light generated directly reflected the amount of infectious virus in the brain. In the recent years, the use of Doppler-echocardiography has become a standard non-invasive technique in the analysis of cardiac malformations in genetically modified mice. Simple collection of unwanted medicines by municipal authorities is unlikely to be effective. Variation in fiber number of a male-specific muscle between Drosophila species: a genetic and developmental analysis. Although BKV DNAemia is a rare event after renal transplantation, it is often associated with BKVAN, which may be treated successfully by the alleviation of immunosuppression and leflunomide therapies. Relaxation cipro dose in uti of coronary arterial smooth muscle and depolarization of cell membrane potential by selenium. On the other hand, acetylated tubulin is present in a few microtubules in pachytene spermatocytes and in the axial filament (precursor of the sperm tail) in round spermatids.

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