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Kleromicin (Clarithromycin)

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Kleromicin is used to treat certain bacterial infections, such as pneumonia (a lung infection), bronchitis (infection of the tubes leading to the lungs), and infections of the ears, sinuses, skin, and throat. Kleromicin is used to treat and prevent disseminated Mycobacterium avium complex (MAC) infection [a type of lung infection that often affects people with human immunodeficiency virus (HIV)].

Other names for this medication:
Abbotic, Biotclarcin, Clabact, Clacee, Clacina, Clarimac, Clarimax, Clarimed, Claripen, Clariston, Clarithromycin, Claritt, Clarix, Clarogen, Claron, Claryl, Clarytas, Cleanomisin, Cleron, Clormicin, Ezumycin, Finasept, Fromilid, Geromycin, Glartin, Hecobac, Karin, Klarimac, Klarithran, Kleromicin, Larizin, Laromin, Likmoss, Lyoclar, Macladin, Maclar, Macromicina, Nutabact, Onexid, Quedox, Rocin, Rodizim, Xylar

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Also known as: Clarithromycin


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


The recommended daily dosage is 15 mg/kg/day divided every 12 hours for 10 days (up to the adult dose). Refer to dosage regimens for mycobacterial infections in pediatric patients for additional dosage information.

For the treatment of disseminated infection due to Mycobacterium avium complex (MAC), Kleromicin Filmtab and Kleromicin Granules are recommended as the primary agents. Kleromicin Filmtab and Kleromicin Granules should be used in combination with other antimycobacterial drugs (e.g. ethambutol) that have shown in vitro activity against MAC or clinical benefit in MAC treatment.

For treatment and prophylaxis of mycobacterial infections in adults, the recommended dose of Kleromicin is 500 mg every 12 hours.

For treatment and prophylaxis of mycobacterial infections in pediatric patients, the recommended dose is 7.5 mg/kg every 12 hours up to 500 mg every 12 hours.

Kleromicin therapy should continue if clinical response is observed. Kleromicin can be discontinued when the patient is considered at low risk of disseminated infection.


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


Store Kleromicin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Kleromicin out of the reach of children and away from pets.

Side effects

The most common side effects associated with Kleromicin 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.


Do not take Kleromicin if you are allergic to its components or to clarithromycin or to similar medicines such as azithromycin (Zithromax), dirithromycin (Dynabac), erythromycin (E.E.S., E-Mycin, Ery-Tab, Erythrocin), troleandomycin (Tao). Do not take Kleromicin if you're pregnant or you plan to have a baby, or you are a nursing mother. Do not take Kleromicin if you take astemizole (Hismanal), cisapride (Propulsid), ergot medicine such as ergotamine (Ergomar, Ergostat, Cafergot, Ercaf, Wigraine), or dihydroergotamine (D.H.E. 45, Migranal Nasal Spray), pimozide (Orap), terfenadine (Seldane). Do not take Kleromicin if you have liver disease, kidney disease, myasthenia gravis, porphyria; personal or family history of "Long QT syndrome". Try to be careful with Kleromicin usage in case you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement. Avoid consuming alcohol. It can be dangerous to stop Kleromicin taking suddenly.

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Using an additional chimera and site-directed mutagenesis, we have determined that a single amino acid, F586, is responsible for increased sensitivity to imipramine, desipramine, and nortriptyline. A simple, group-level educational outreach intervention, designed to take account of identified barriers to change, can have a modest but sustained effect on prescribing levels. Formula sterilization recommendations by physicians and sterilization practices by mothers need to be updated. The age was under 14 years for 18 patients, between 14 and 25 for 10 patients, and more than 25 for the remaining 17 patients. Free erythrocyte protoporphyrin (FEP) and hemoglobin concentrations in 788 children were investigated during routine check-ups in a private pediatric practice. Here, we investigate the effect of Curosurf on the pulmonary synthesis of sPLA(2)-IIA in this ALI model. However, data presented here demonstrate that FV3 does not replicate in UV-irradiated or enuleated chicken embryo or BSC-1 cells and that virus-specific DNA synthesis is not initiated in such cells. Influence of formulation on oral drug delivery: considerations for generic substitution and selection of slow-release products. However, drug studies demonstrate that both filamentous actin and microtubules are required for lobe formation. We have demonstrated that carbohydrates in Cry j 1, the major allergen of Cryptomeria japonica pollen, play a major role in promoting Cry j 1-specific Th2 response.

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Large overlapping home ranges in males, lack of sexual size dimorphism, and relatively large testes suggest a multi-male mating system, i.e., one that is promiscuous rather than polygynous. Calpain, a calcium-dependent cysteine protease, plays an essential role in basic cellular processes in animal cells, including cell proliferation, apoptosis, and differentiation. Neisseria gonorrhoeae (the gonococcus, Gc) is the causative agent of gonorrhoea, and has evolved several systems for varying the antigenicity of different surface antigens, presumably to help evade the effects of the human immune system. 100 patients were randomized to receive either placebo or dexamethasone (1 mg/ kg, at induction of anesthesia and 0.5 mg/kg 8 h later). Strategies for the modification of risk factors in gynecological cancers.

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