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Althromicin (Clarithromycin)
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Althromicin

Althromicin is an antibiotic. It stops the bacteria from growing, which helps cure your infection. Althromicin is taken orally, preferably either one hour before or 2 hours after a meal. Althromicin is also effective against some infections (e.g., MAC or Mycobacterium avium complex) seen in people with reduced immunity.

Other names for this medication:
Bicrolid, Cidoclar, Clabel, Clacine, Clamycin, Clarimac, Clarimycin, Clarithromycin, Claritron, Claritrox, Claritt, Cleanomisin, Clonocid, Derizic, Egelif, Eracid, Heliclar, Infex, Kailasa, Karid, Klabion, Klaritpharma, Kofron, Laromin, Macladin, Macromicina, Monozeclar, Xylar, Zeclaren

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Also known as: Clarithromycin

Description

Althromicin is used to treat many different types of bacterial infections affecting the skin and respiratory system. Althromicin is also used together with other medicines to treat stomach ulcers caused by Helicobacter pylori. Althromicin fights bacteria in the body. Althromicin is also known as Clarithromycin, Maclar, Klaricid, Klacid, Clarimac, Claribid.

Dosage

This section provides information on the proper use of a number of products that contain clarithromycin. It may not be specific to Althromicin Filmtab. 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.

You may take this medicine with meals or milk or on an empty stomach. However, clarithromycin extended release tablets should be taken with food.

If you are using the extended-release tablets:

Swallow the tablet whole. Do not break, crush, or chew it. While taking the extended-release form of this medicine, a part of the tablet may pass into your stools. This is normal and is nothing to worry about.

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

If you are taking clarithromycin and zidovudine, these medicines should be taken at least 2 hours apart.

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

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 tablets): For bacterial infections: Adults—1000 milligrams (mg) once a day for 7 to 14 days. Children—Use and dose must be determined by your doctor. For community-acquired pneumonia: Adults—1000 milligrams (mg) once a day for 7 days. Children—Use and dose must be determined by your doctor. For oral dosage forms (suspension and tablets): For bacterial infections: Adults—250 to 500 milligrams (mg) every 12 hours for 7 to 14 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 7.5 milligrams (mg) per kilogram (kg) of body weight every 12 hours for 10 days. Infants younger than 6 months of age—Use and dose must be determined by your doctor. For community-acquired pneumonia: Adults—250 milligrams (mg) every 12 hours for 7 to 14 days. Children 6 months of age and older—Dose is based on body weight and must be determined by your doctor. Infants younger than 6 months of age—Use and dose must be determined by your doctor. For prevention or treatment of Mycobacterium avium complex (MAC) infection: Adults—500 milligrams (mg) 2 times a day. Children 20 months of age and older—Dose is based on body weight and must be determined by your doctor. The dose is usually 7.5 milligrams (mg) per kilogram (kg) of body weight, up to 500 mg, 2 times a day. Children younger than 20 months of age—Use and dose must be determined by your doctor. For treatment of ulcers associated with H. pylori: Adults—500 milligrams (mg) every 8 hours for 14 days in combination with omeprazole, 500 mg every 12 hours in combination with amoxicillin and lansoprazole for 10 or 14 days, or 500 mg every 12 hours in combination with amoxicillin and omeprazole for 10 days. Children—Use and dose must be determined by your doctor.

Overdose

If you overdose Althromicin and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Althromicin overdosage: nausea, vomiting, diarrhea, abdominal discomfort.

Storage

Store Althromicin XL Filmtab at 20 to 25 degrees C (68 to 77 degrees F). Excursions permitted to 15 to 30 degrees C (59 to 86 degrees F).

Side effects

The most common side effects associated with Althromicin 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

Appropriate studies have not been performed on the relationship of age to the effects of clarithromycin to treat bacterial infections in children younger than 6 months of age, and to prevent and treat Mycobacterium avium complex in children younger than 20 months of age. Safety and efficacy have not been established in these age groups.

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Cardiac and hemodynamic effects of the centrally acting analgesics tramadol and pentazocine in anaesthetized rabbits and isolated guinea-pig atria and papillary muscles. To assess the outcomes of small optical zone (OZ) ablations used in conjunction with large transition zones (TZ) and a highly aspheric treatment profile. HSC/P localization and migration between niches depend on cell-cell and cell-matrix interactions, which result from the cooperation of cytokines, chemokines and adhesion molecules. The DeltaExt/R4Tth protein also induced formation of densely packed membrane stacks in the cytosol and we suggest a model were the intranuclear structures are formed by invagination of ER-derived membrane stacks into the nucleus. Further studies are needed to replicate this finding, and to investigate the impact of other genetic markers of vascular disease on late-life depression outcome.

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Cell cycle arrest in response to DNA damage involves protein stabilization and consequent upregulation of p53, which induces transcription of cyclin-dependent kinase inhibitor p21 (CDKN1A). Bacterial quantification revealed high levels of Staphylococcus xylosus in the corneas of CD36(-/-) mice with severe defects, but not in wild-type controls. Ex vivo cultured bronchoalveolar lavage (BAL) cells isolated from patients with sarcoidosis and control subjects were stimulated with low-dose Toll-like receptor 4 (TLR4) and nucleotide-binding oligomerization domain 1 (NOD1) ligands as a model of microbial stimulation, and MAPK signaling and inflammatory response were analyzed. Low time settings were used to avoid loss of detail through movement and to minimize exposure while observing radiation safety. Feasibility of source identification of seized street drug samples by exploiting differences in isotopic composition at natural abundance level by GC/MS as compared to isotope ratio mass spectrometry (IRMS). How calmodulin binds its targets: sequence independent recognition of amphiphilic alpha-helices.

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The nature and treatment of the three major types of juvenile rheumatoid arthritis--systemic, polyarticular, and pauciarticular--are presented. One of the strong assets of cardiac magnetic resonance (CMR) is its ability to assess myocardial anatomy, structure, function, flow, and perfusion within a single examination. Novel small RNA (sRNA) landscape of the starvation-stress response transcriptome of Salmonella enterica serovar typhimurium. The enhancement effect of TNF is dose-dependent, reaching a maximum at approximately 50 U/mL. The aim of this review is to summarize recent findings dealing with the biochemical properties and the biological functions of 8-OH-G rhinocort generic equivalent DNA glycosylases in bacterial, yeast, insect and mammalian cells. Probenecid inhibits the renal secretion of drug glucuronides and this will lead to accumulation in plasma of those NSAIDs eliminated primarily by the formation of labile acyl glucuronides such as naproxen, ketoprofen, indomethacin, carprofen. Early recognition of the syndrome, closed monitoring and vigorous treatment can prevent maternal complications and/or fetal distress. The authors present cases, in which imaging diagnostic studies, implemented therapeutic procedures and numerous consultations have not prevented misdiagnosing the patients and their resultant death. Rolapitant is a long-acting NK-1 receptor antagonist with proven efficacy in controlling CINV as part of the prophylaxis regimen.

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