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Abbotic (Clarithromycin)

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

Other names for this medication:
Aeroxina, Bicrolid, Clacee, Clarimed, Clarimycin, Claripen, Claritrox, Claritt, Claromycin, Claxid, Clormicin, Derizic, Eliben, Euromicina, Ezumycin, Gervaken, Karid, Klarifor, Klariger, Klarimax, Klarit, Klerimed, Kofron, Laromin, Lekoklar, Nutabact, Rodizim, Rolicytin

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Also known as: Clarithromycin


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


This section provides information on the proper use of a number of products that contain clarithromycin. It may not be specific to Abbotic. 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 symptoms may include severe stomach pain, nausea, vomiting, or diarrhea.


Store Abbotic 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 Abbotic 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.


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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Surface and intracellular (Foxp3) T-reg markers were evaluated by flow cytometry. To the best of our knowledge, there are no reports of normal pyramidal decussation in JS. Synthesis and progestational activities of some 16-methylene-17 -acetoxy-9 ,10 -pregna-4,6-diene-3,20-dione derivatives. Effects of interleukin 2 therapy in patients with common variable immunodeficiency (CVID). Focal nodular hyperplasia of the liver: assessment of diagnosis and treatment in 31 patients in 15 years. The BSRV-like sequences represent a potentially novel dicistrovirus infecting A. Eighteen of these patients attempted suicide by overdosing moclobemide with or without other drugs. The heavy chain of the same IgM RF clone had a blocked N-terminus, but a cyanogen bromide peptide starting after methionine at position 82 showed a sequence typical of the VHIII subgroup.

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A prospective survey over a two-year period 1988-1990 of all cases diagnosed as having leptospirosis at Victoria Hospital, the main referral hospital for the Islands. However, up to now, our understanding on the mode of action of the TCD is still limited. Note from a Concerned American Citizen, an Infection and Immunity and mBio Editor, and a Scientist with Puerto Rican Roots. In order to prepare SiO(2) nanoparticles that are dispersible in various organic solvents, an anionic surfactant 1, which branches into a hydrophobic chain and a hydrophilic chain, was adsorbed on to SiO(2) nanoparticles through a layer-by-layer surface modification route using polyethyleneimine (PEI). On five in vitro models, half of the maxilla from dry skulls, special designed splints with a Troll-biten film holder were constructed.

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IFN gamma-activated macrophages were able to phagocytize a greater number of EIgG before a decrease in PMA-triggered H2O2 production was observed and the level of H2O2 production did not fall below that of untreated-inflammatory macrophages that had not received an EIgG phagocytic challenge. IgH repertoire and Ig-related gene expression in X-linked agammaglobulinemia. Possible mechanisms of the novobiocin effect on DNA and RNA synthesis are discussed. Background variables did not affect the results to any major degree. Gender differences and factors associated with the receipt of thrombolytic therapy in patients with acute myocardial infarction: a community-wide perspective. In addition, similar vibration artifact also occurred in the limbic depth, indicating that at least some respiration-linked intracerebrally recorded limbic spindles also are not of neuronal origin. Investigations on the chromosomal localizations of the human and chimpanzee interferon genes: possible role of chromosomes 9 and 13. Golgi stains revealed that classically defined dendrites of supraoptic neurons projected primarily ventrally and often invaded the ventral glial lamina. Proteolytic enzyme inhibitor activity has been measured in the rheumatoid knee by 2 different techniques. Hip fracture management, before and beyond surgery and medication: a synthesis of the evidence.

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Addition of human, recombinant interleukin-1 beta (hrIL-1 beta) to cultures of lapine articular chondrocytes provoked a delayed increase in the production of both nitric oxide (NO) and lactate. Accumulation of 2-HG can result in epigenetic dysregulation and a block in cellular differentiation, suggesting these mutations play a role in neoplasia. The peritoneal fluid from patients with endometriosis also reacted with 34-kd endometrial antigen but not the peritoneal fluid from control fertile women. TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. A patient complaining of pain and noise on turning her neck was diagnosed as having a large greater cornua of the hyoid bone. Direct probing of the adsorbate-substrate chemical bond using angle-dependent x-ray-emission spectroscopy. Radiation-induced changes in the breast: a potential diagnostic pitfall on fine-needle aspiration. Longitudinal studies have contributed substantially to understanding of aging and geriatric syndromes. Kappa Opioid receptors (KORs) change the impact of apelin on the phosphorylated ERK1/2 (pERK1/2).

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The samples were extracted by acetonitrile, further concentrated and purified by an Oasis MCX cartridge, and then the contents of thiabendazole and 5-hydrothiabendazole in tissue homogenates determinated by liquid chromatography electrospray ionisation tandem mass spectrometry (UPLC-ESI-MS/MS). Studies on the effects of nitrendipine on oxytocin-, angiotensin II- and ergometrine-induced contraction of pregnant human myometrium in vitro. Circumcision, electric fulguration and excision of urethral tumor were performed. Our study indicate Threshold Accepting as a better technique in locating such structures. The authors examined a cohort of SCCHNs using a previously developed biomarker combination that likely predicts p53 status based on p53/MDM2 expression levels determined by immunohistochemistry (IHC). The capacity of phenol/water extracted lipopolysaccharides (LPS) from Bacteroides, Fusobacterium and Veillonella to induce histamine release from rat peritoneal mast cells has been evaluated by means of a bioassay using atropinized guinea pig ileum and a fluorescence assay. It concern also plasmapheresis as a special effective procedure in toxic forms of the diphtheria. A systematic review of factors affecting vaccine uptake in young children. We also highlight the potential of our results in a therapeutic perspective for brain cancer that could be generalized for other cancers.

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