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Azadose (Azithromycin)
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Azadose

Azadose is a Tablet manufactured by Cipla. It is commonly used for the diagnosis or treatment of Bronchitis, Throat infection, Lung infection, Sexaully transmitted disease, Urinary infections.

Other names for this medication:
Altezym, Azadose, Azifast, Azimakrol, Azimax, Azinom, Azithrocin, Azithrocine, Azithromax, Azitropharma, Azitrovid, Azomex, Bactexina, Fabramicina, Gramokil, Hemomycin, Macromax, Macrozit, Mezatrin, Neblic, Sumamed, Trozocina, Zaret, Zertalin, Zibac, Zithrocin, Zithrox, Zitroken, Zymycin

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Also known as: Azithromycin

Description

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

Azadose 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.

Azadose 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.

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

Dosage

Use Azadose as directed by your doctor.

Take Azadose by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

Do not take an antacid that has aluminum or magnesium in it within 1 hour before or 2 hours after you take Azadose.

Azadose works best if it is taken at the same time each day.

To clear up your infection completely, use Azadose 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 Azadose.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

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 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

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome: diarrhea; headache; loose stools; nausea; stomach pain; upset stomach; vomiting.

Seek medical attention right away if any of these severe side effects occur: severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); bloody stools; changes in hearing or hearing loss; chest pain; eye or vision problems; irregular heartbeat; muscle weakness; pounding in the chest; red, swollen, blistered, or peeling skin; ringing in the ears; seizure; severe diarrhea; stomach cramps/pain; trouble speaking or swallowing; yellowing of the skin or eyes.

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Anti-viral agents incorporating sulfamate moieties have also been obtained, with at least two types of such derivatives investigated: the nucleoside/nucleotide human immunodeficiency virus (HIV) reverse transcriptase inhibitors, and the HIV protease inhibitors (PIs). VIP levels were measured by radioimmunoassay in peripheral venous blood of conscious dogs. One of the intracellular targets for NO action is glutathione (GSH). The roles played by different peach allergens with respect to symptom severity have not been completely ascertained. This study investigated signalling downstream of the receptors activated by H2 O2 . To evaluate the efficacy and safety of rosuvastatin in postmenopausal women with hypercholesterolemia who are receiving hormone replacement therapy (HRT) in a randomized, double-blind, placebo-controlled trial. However, detailed analyses of these trends and programs to address them are lacking. The control quadrant was treated by scaling and root planing only, while the other two test quadrants were treated by intra-pocket application of gel combined with scaling or root planing and topical applications combined with scaling and root planning, respectively.

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In contrast, treatment of A27/80 and OVCAR-3 epithelial ovarian cancer cells with IFNgamma stimulated H-REV107-1 expression. Long-term drug prevention of cardiovascular diseases (methodological aspects). Duration of daily sunshine was significantly correlated with suicide frequency independent of season, but effect sizes were low. The viral genome was detected in cerebrospinal fluid and stool by reverse transcription polymerase chain reaction. At the start of the study the children with Down syndrome were 17 to 19 months old. These relationships were stronger when differences in body size were controlled for statistically, and were consistent between two phylogenies and when species were treated as independent data points.

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