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Azadose (Azithromycin)
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Azadose

Azadose 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:
Amovin, Azalid, Azatril, Azidraw, Azimax, Azimycin, Azinix, Azirox, Azithromycin, Azithromycinum, Azitrom, Azitrox, Azomac, Bezanin, Faxin, Goxil, Gramokil, Ilozin, Neblic, Novozithron, Novozitron, Opeazitro, Sitrox, Tanezox, Tromix, Zibramax, Zimax, Zinfect, Zirocin, Zitrocin, Zitrofar, Zitroken, Zitrotek, Zomax

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Also known as: Azithromycin

Description

The drug is an antibiotic used to treat a variety of bacterial infections, such as cat-scratch disease, ear infections, infections of the skin or surrounding tissue, and throat or tonsil infections.

Azadose is also used to treat lung and other respiratory infections, such as bronchitis, sinusitis, community acquired pneumonia, some cases of chronic obstructive pulmonary disease (COPD), and whooping cough (pertussis).

Doctors may also prescribe azithromycin for genital infections and sexually transmitted diseases, such as gonorrhea, infections of the urethra or cervix, genital ulcers, and severe pelvic inflammatory disease.

Azadose belongs to group of drugs known as macrolide antibiotics. They work by preventing bacteria from making their own proteins.

As with other antibiotics, to prevent the spread of drug-resistant infections, the Food and Drug Administration (FDA) strongly advises doctors to prescribe the drug only when there is proof, or a strong suspicion, that the infection is caused by bacteria against which Azadose is effective.

The FDA first approved Azadose under the brand name Zithromax in 1991. Pfizer Pharmaceuticals manufactures the drug.

Dosage

A nurse or other trained health professional will give you this medicine. This medicine is given through a needle placed in one of your veins. This medicine is given slowly, so the needle will remain in place for about an hour.

Your doctor may give you a few doses of this medicine until your condition improves, and then you may be switched to an oral medicine that works the same way. If you have any concerns about this, talk to your doctor.

Detailed Azadose dosage information

Overdose

Adverse reactions experienced at higher than recommended doses were similar to those seen at normal doses particularly nausea, diarrhea, and vomiting. In the event of overdosage, general symptomatic and supportive measures are indicated as required.

Storage

Store medicines at room temperature, away from heat and direct light. Do not freeze medicines unless required by package insert. Keep medicines away from children and pets.

Do not flush medications down the toilet or pour them into drainage unless instructed to do so. Medication discarded in this manner may contaminate the environment. Please consult your pharmacist or doctor for more details on how to safely discard Azadose Tablet.

Side effects

The most common side effects associated with Azadose 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

Hypersensitivity to Azadose and other macrolide antibiotics.

Azadose 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 Azadose in the lactation period should solve the issue of termination of breastfeeding.

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

Azadose 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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Interaction of platinum drugs with clinically relevant x-ray doses in mammalian cells: a comparison of cisplatin, carboplatin, iproplatin, and tetraplatin. Here, we report the first example of a D-2-hydroxyacid dehydrogenase with dual coenzyme-specificity. It is apparent that alterations in lens surface properties, wear protocol, and application of the device are not significant in determining deposit morphology. Pontifical council for family--note on the natural regulation and methods of observing fertility. Autoimmunization against the neutrophil-specific NA1 antigen is associated with HLA-DR2. Individual cultures were also immobilized and uptake of phenol by the immobilized micro-organisms was observed in a nutrient-rich and nutrient-stressed medium containing phenol as a sole source of carbon. To compare full-threshold (FT) and SITA algorithms for standard automated perimetry (SAP) with frequency-doubling technology perimetry (FDT) in glaucoma, to help clinicians to relate results in patients who have had two or more of these tests during follow-up.

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Posttranslational modifications can cause profound changes in protein function. Optimum number of mixed peripheral blood samples by membrane filtration technique for mass blood survey of filariasis. The pharmacological study of these compounds confirms that modification of the chemical group at position 5 of the 6-phenyl-3(2H)-pyridazinone system influences both variations in the antiplatelet activity and the mechanism of action. Thus, the hCdc14A phosphatase appears to play a role in the regulation of the centrosome cycle, mitosis, and cytokinesis, thereby influencing chromosome partitioning and genomic stability in human cells. Activating mutations of the receptor tyrosine kinase, ret, are associated with multiple endocrine neoplasia type 2A (MEN 2A). Specifying the role of mu- and m-calpain using antisense oligonucleotides led to show that both calpains up-regulate alpha- and beta-actin in ARMS cells. An understanding of these biases is essential when designing such studies and when interpreting the results of existing studies. Trichinella spiralis infection in congenitally athymic (nude) mice. To ensure maximal repression in normal cells, the inclusion of additional E-boxes in the proximal region of the core promoter was described.

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Functional identification of secondary mutations inducing autonomous growth in synergy with a truncated interleukin-3 receptor: implications for multi-step oncogenesis. Five excellent articles representing the research in four different nations were selected for the IMIA Yearbook 2006 from three international peer reviewed journals. Clinical significance of micrometastasis in lung and esophageal cancer: a new paradigm in thoracic oncology. The trigger factor is the first molecular chaperone interacting with virtually all newly synthesized polypeptides on the ribosome and also possesses a peptidyl-prolyl cis-trans isomerase activity. Plasma concentrations of the enantiomers and their corresponding pyridine metabolites were determined by g.l.c.-mass spectrometry. The presence of HSP 90 in the PRA 8S complex was confirmed by use of an HSP 90-specific antibody, AC-7. DES use resulted in lower rates of clinically driven repeat revascularization with similar rates of stent thrombosis. All patients who suffered from an episode of APAC at two Singapore hospitals over a one-year period underwent static automated threshold perimetry six months after presentation. Evaluation of cefmetazole and piperacillin with or without tobramycin for infections in patients with hematological disorders. Multivariate Cox proportional hazards models and Kaplan-Meier curves were constructed to examine the association between pelvic radiation and the development of subsequent hematologic malignancies.

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