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Azimex (Azithromycin)
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Azimex

Azimex is used to treat various bacterial infections of the respiratory system, skin infections, ear infections, and sexually transmitted infections. Azimex is used to treat various bacterial infections of the respiratory system (like pneumonia, bronchitis, tonsillitis, pharyngitis and sinusitis), skin infections (like acne and rosacea), ear infections, and sexually transmitted infections.

Other names for this medication:
Altezym, Azicip, Azimakrol, Azimit, Azimycin, Azinom, Azithral, Azithromycin, Azithrox, Azitral, Azitro, Aziwok, Azomax, Azomycin, Azrolid, Azyter, Bactexina, Binozyt, Doromax, Fabramicina, Faxin, Iramicina, Maczith, Neofarmiz, Opeazitro, Oranex, Tritab, Tromix, Ultrabac, Zithromac, Zithrox, Zitrex, Zival

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Also known as: Azithromycin

Description

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

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

Follow all directions on your prescription label and read all medication guides or instruction sheets. Use the medicine exactly as directed.

Azimex Z-Pak oral is taken by mouth. This medicine injection is given as an infusion into a vein, usually for 2 days before you switch to this medicine oral. A healthcare provider will give you this injection.

You may take Azimex Z-Pak oral with or without food.

Shake the oral suspension (liquid) before you measure a dose. Use the dosing syringe provided, or use a medicine dose-measuring device (not a kitchen spoon).

Use Azimex Z-Pak for the full prescribed length of time, even if your symptoms quickly improve. Skipping doses can increase your risk of infection that is resistant to medication. Azimex Z-Pak 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 Azimex dosage information

Overdose

If you overdose Azimex and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Azimex 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 Zmax® extended-release oral suspension. 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 Azimex® 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.

Detailed Azimex dosage information

Side effects

The most common side effects associated with Azimex 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

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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Use of Yokukansan (TJ-54) in the treatment of neurological disorders: a review. Role of persistent CMV infection in configuring T cell immunity in the elderly. The locus is arranged as a large operon containing six open reading frames whose expression is specifically induced during the interaction with host plants. Influencing solvent miscibility and aqueous stability of aluminum nanoparticles through surface functionalization with acrylic monomers. We conclude that heterozygous substitutions at the AGT M235T and REN A/G(I8-83) loci correlate significantly with ESRD in a north Indian population. Additional outcomes included symptomatic intracranial haemorrhage (defined by type 2 parenchymal haemorrhage within 7 days and, separately, by the SITS-MOST definition of parenchymal type 2 haemorrhage within 36 h), fatal intracranial haemorrhage within 7 days, and 90-day mortality. A telephone survey was conducted to collect information from discharge to 8 months after discharge for 433 patients hospitalized with a primary diagnosis of ACS in 5 mid-Michigan hospitals. American College of Physicians-American Society of Internal Medicine.

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Chemical probing and mutagenesis demonstrate that the central domain is stabilized by a pseudoknot. (18)F-FDG microPET and hyperinsulinemic-euglycemic clamp analyses demonstrated increased glucose uptake into white and brown adipose tissue, but not into skeletal muscle of Par-1b null mice relative to wild-type controls. Identification of tyrosine phosphorylations of band 3, band 4.2, catalase and actin which have not been previously described in P. Age differences in the incidence of A2/Hong Kong influenza in patients belonging to different blood groups. In vivo femtosecond laser subsurface scleral treatment in rabbit eyes.

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To determine an estimate of the period prevalence of medically attended injury in West Virginia via a statewide random telephone survey. A method for performing semi-automatic lesion segmentation based on a supervised learning formulation was compared with the enhancement threshold based segmentation method in the context of a computer-aided diagnostic system. The results were as follows: 1) Repeated myringotomies caused a dramatically thickened TM in not only the operated area, but also the posterior quadrants. Exposure to PUVA induced an increase in p53 expression in non-lesional skin in 14/19 patients, putatively as a response to DNA damage caused by PUVA. Forty-four hours after EB, 0.5 mg progesterone (P) was injected and a behavioral test was started 4 h after P. The different pattern of IGFBP secretion depends on the anatomical district and on the species of the tissues.

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A method of determining the initial rate of plasminogen activation has been developed. Renal function parameters of Thai vegans compared with non-vegans. The epitope of an immunogenic peptide can be partially replaced with peptide fragments from various pathogens without any detrimental effect to their anchoring within the binding groove of MHC class II molecules. Microvascular reconstruction should be used as the first-line strategy for these patients, with APS indicated only when the artery is unable to be microscopically anastomosed. We tested the hypothesis that intensified management of gestational diabetes mellitus on the basis of stringent glycemic control, verified glucose data, and adherence to an established criterion for insulin initiation results in near normoglycemia control and reduction of adverse outcomes. Effect of hyporeactivity (tolerance) to a viral interferon inducer on the transplantation of Krebs 2 ascitic carcinoma cells in mice. We recently showed that in rheumatoid arthritis (RA) the extracellular matrix around the lining cells is similar to the matrix seen in osteoarthritis, whereas the cellular adhesion apparatus is very different. Clinical and virologic follow-up in perinatally HIV-1-infected children and adolescents in Madrid with triple-class antiretroviral drug-resistant viruses.

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