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Azitrotek (Azithromycin)
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Azitrotek

Azitrotek is used to treat many different types of infections caused by bacteria, such as respiratory infections, skin infections, ear infections, and sexually transmitted diseases. In children, it is used to treat middle ear infection, pneumonia, tonsillitis, and strep throat.

Other names for this medication:
Arzomicin, Atizor, Azicid, Azicu, Azigram, Azinix, Azithral, Azithrex, Azithromax, Azithromycin, Azithromycinum, Azitral, Azitro, Azitrobac, Azitromicina, Azomac, Azomex, Azomycin, Azrolid, Azromax, Azyter, Bezanin, Binozyt, Clearsing, Doromax, Ericiclina, Goldamycin, Magnabiotic, Momicine, Nifostin, Novozitron, Oranex, Orobiotic, Penalox, Pretir, Rozith, Sumamed, Texis, Thiza, Zemycin, Zibac, Zifin, Zimax, Zirocin, Zistic, Zithrogen, Zitrim, Zitroneo, Zitrotek, Zycin

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Also known as: Azithromycin

Description

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

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

This section provides information on the proper use of a number of products that contain azithromycin. It may not be specific to Azitrotek Tri-Pak. Please read with care.

Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.

This medicine comes with a patient information leaflet. Read and follow the instructions carefully. Ask your doctor if you have any questions.

You may take Azitrotek® oral liquid or tablets with or without food.

Shake well the bottle of Azitrotek® oral liquid before each use. Measure your dose correctly with a marked measuring spoon, oral syringe, or medicine cup. The average household teaspoon may not hold the right amount of liquid.

Measure the Zmax® extended-release oral suspension with a marked measuring spoon, syringe, or cup. You or your child must take this medicine within 12 hours after it has been mixed with water. It is best to take the Zmax® extended-release oral suspension on an empty stomach or at least 1 hour before or 2 hours after a meal. If your child does not use all of the medicine in the bottle, throw it away after you give the dose.

If you or your child vomits within one hour of taking the Zmax® extended-release oral suspension, call your doctor right away to see if more medicine is needed.

Keep using this medicine for the full treatment time, even if you or your child feel better after the first few doses. Your infection may not clear up if you stop using the medicine too soon.

If you are taking aluminum or magnesium-containing antacids, do not take them at the same time that you take Azitrotek®. These medicines may keep azithromycin from working properly. However, you can take antacids with Zmax®.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For oral dosage form (extended-release suspension): For treatment of pneumonia: Adults—2 grams (g) once as a single dose. Children weighing 34 kilograms (kg) or more—Dose is based on body weight and must be determined by your doctor. The dose is usually 2 grams once a day, taken as a single dose. Children 6 months of age and older weighing less than 34 kg—Dose is based on body weight and must be determined by your doctor. The dose is usually 60 milligrams (mg) per kilogram (kg) of body weight once a day, taken as a single dose. For treatment of sinusitis: Adults—2 grams (g) once a day as a single dose. Children—Use and dose must be determined by your doctor. For oral dosage forms (suspension or tablets): For treatment of infections: Adults—500 to 2000 milligrams (mg) once a day, taken as a single dose. Depending on the type of infection, this may be followed with doses of 250 to 500 mg once a day for several days. Children 6 months of age and older—Dose is based on body weight and must be determined by your doctor. The dose is usually 10 to 30 milligrams (mg) per kilogram (kg) of body weight once a day, taken as a single dose. Depending on the type of infection, this may be followed with doses of 5 to 10 mg per kg of body weight once a day for several days. Children younger than 6 months of age—Use and dose must be determined by your doctor. For treatment of pharyngitis or tonsillitis: Adults—500 milligrams (mg) on Day 1 (the first day), taken as a single dose. Then, 250 mg on Day 2 through Day 5. Children 2 years of age and older—Dose is based on body weight and must be determined by your doctor. The dose is usually 12 milligrams (mg) per kilogram (kg) of body weight once a day for 5 days. Children younger than 2 years of age—Use and dose must be determined by your doctor.

Overdose

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

Storage

Store Azitrotek below 86 degrees F (30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Azitrotek out of the reach of children and away from pets.

Side effects

The most common side effects associated with Azitrotek 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

Azitrotek is contraindicated in patients with known hypersensitivity to azithromycin, erythromycin, any macrolide or ketolide drug.

Azitrotek is contraindicated in patients with a history of cholestatic jaundice/hepatic dysfunction associated with prior use of azithromycin.

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Assessment of the prevalence of iron deficiency anemia, by serum ferritin, in pregnant women of Southern Iran. BMY 30047 (11-cis, 13-cis-12-hydroxymethylretinoic acid delta-lactone) is one of a series of retinoic acid derivatives in which the carboxyl function of the polar end was modified with the aim of achieving reduced local irritation and systemic toxicity while retaining the local therapeutic effect. The data of some large cohort followed prospectively such as the European cohort (1000 APS patients) as well the data of some registries (APS in children and patients with a catastrophic APS) bring some new important information on the clinical aspects of the syndrome. For the first time data from the present study provide a direct molecular link between PGE(2) signaling and proliferation of endometriotic cells and suggest that inhibition of EP2/EP4 could be a potential nonestrogen (E) treatment option for endometriosis in women. Dynamic and site-specific impact of ventricular pacing on left ventricular ejection fraction. Beyond supportive measures, the care of infants with bronchiolitis remains controversial. Long-term survival after permanent pacemaker implantation: analysis of predictors for increased mortality. The aim of this study is to evaluate and compare self-esteem, coping strategies and feeling of anger in French populations with anorexia nervosa. Unlike IL-2-dependent activation of JAK/STAT pathways, activation of Akt kinase was impaired after MV contact both in vitro and in vivo.

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In the past year, several provocative studies have presented evidence that autoantibodies may actually cause the vascular damage and fibrosis characteristic of systemic sclerosis. Furthermore, the expression of bcl-2 and bax genes involved in apoptosis as well as tumor-associated p65 gene were determined. Biodiversity surveys are often hampered by the inability to control extraneous sources of variability introduced into comparisons of populations across a heterogenous landscape. The atypical antipsychotics quetiapine, risperidone and ziprasidone do not increase insulin release in vitro. A tensile-testing machine was used to gauge isometric muscle force of the plantaris and both heads of the gastrocnemius muscle. TK activity significantly decreased concomitantly with this arrest in weight gain, while in contrast TS activity was not depressed. Determination of the optimal stylet strategy dose of rocaltrol for the C-MAC videolaryngoscope. The Micropaque injection was injected either by an ascending route in the thoracic aorta or by a descending route in the left internal carotid below the ductus arteriosus.

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Statistical studies were made on 1,795 outpatients, 528 inpatients and 518 operative procedures at our department in 1985. There were 6 boys and 3 girls ranging in age from 3 months to 29 months. Granular activated carbon was used as the attachment medium for biological growth. In this review, we discuss the EPO-induced activation of endothelial nitric oxide (NO) synthase and its contribution to the prevention of cerebral vasospasm. Three specialized rhythm analysing programmes allowing one to get the description and graphic image of variability and rhythm structure and the reaction on tricor medication names its influence are stated. In both primary and secondary spongiosae, the loss of trabecular bone was more extensive in flight rats than in suspended rats. To test the biocompatibility of this brushite, cellular response to the transformation needs to be understood. The mandatory minute volume mode is based on a complicated program of a cautious nature which reacts instantly to inadequate spontaneous breathing, but is slow to discontinue artificial ventilation. The highly sensitive method can be used in future health risk assessment of AA exposure, such as those in fast-food restaurants.

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Activation of the immediate-early gene c-fos through MAP kinases is a hallmark of growth factor signaling. Primary (idiopathic) thrombocythaemia is a rare disease in childhood. The histologic and cytologic findings showed distinct variability in most patients, with atypia or even absence of malignant cells often followed by recurrence. Up to now, more than 1000 cochlear implants have been accomplished successfully in Iran. Additional medical history included obstructive sleep apnea, type 2 diabetes, and hypertension. Gentamicin clearly shows in both tests a non-linear correlation between cellular toxicity and concentration or period of contact. The past decade has demonstrated increasing interests in using optimal control based methods within coherent quantum controllable systems. Behavioral dependence upon nicotine can be induced in the rat, and its induction is dependent upon its cumulative duration and pattern of exposure suggesting that tobacco dependencies could be controlled by similar determinants.

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The addition of 2-mercaptoethanol to the culture medium was essential for successful stimulation of lymphocytes by allogeneic kidney cells. Twenty-four patients were randomized to either a low-dose (1.95 g omega-3/day) or a high-dose (4.55 g omega-3/day) supplement. The suggestion on excessive discharge of catecholamines from the sympathetic terminals as the cause of deafferentational disorders is not confirmed. With this in mind, consider how the effects of World War II on the growth of physician anesthesia loosely parallel the growth of anesthesia in Great Britain during the 19th century. As these two factors are able to mediate opposing transcriptional effects by reorganizing the local chromatin environment, the relative levels of NFY and YY1 binding could represent a mechanism for balancing activation and repression of Hoxb4 through the same site. Visual acuity was assessed after recovery from the acute effects of atropine.

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Preparation and characterization of silverfish (Lepisma saccharina) extract and identification of allergenic components. Thus, we concluded that this method is an efficient one for determining drug nephrotoxicity in rats. Knowledge and attitude of 2,000 parents (urban and rural - 1,000 each) with regard to avulsed permanent incisors and their emergency management, in and around Davangere. CHAID analysis proved to be a useful statistical method in predicting female adult criminality after preceding perinatal risks. It is suggested that the two tasks use different resource pools in addition to a common mechanism, the limited capacity of which causes a general interference in dual-task conditions. The effect of modeling during treatment is interpreted in terms of coactive facilitation. Synthesis, antiinflammatory and analgesic activity of new hexahydropyrimidine derivatives.

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