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Antirobe (Clindamycin)

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Antirobe is used for treating serious infections caused by certain bacteria. Antirobe is a lincomycin antibiotic. Antirobe kills sensitive bacteria by stopping the production of essential proteins needed by the bacteria to survive.

Other names for this medication:
Clidets, Climadan, Clinamicina, Clindabuc, Clindamicin, Clindamycine, Clindamyl, Clindareach, Clindastad, Clindaval, Clinsol, Cliofar, Comdasin, Dalacine, Dalcap, Edason, Euroclin, Klindan, Klindaver, Klinoksin, Lindan, Lindasol, Luoqing, Milorin, Opiclam, Paradis, Trexen, Ziana, Zindaclin, Zindacline

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Also known as: Clindamycin


Clindamycin belongs to the family of medicines called antibiotics. Topical clindamycin is used to help control acne. It may be used alone or with one or more other medicines that are used on the skin or taken by mouth for acne. Topical clindamycin may also be used for other problems as determined by your doctor.

Clindamycin is available only with your doctor's prescription.


This section provides information on the proper use of a number of products that contain clindamycin. It may not be specific to Antirobe Pediatric. Please read with care.

Take this medicine exactly 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. To do so may increase the chance of side effects.

Take the capsule with a full glass (8 ounces) of water. This is to prevent irritation of the esophagus (tube between the throat and stomach).

Measure the oral liquid correctly using the marked measuring spoon that comes with the package. The average household teaspoon may not hold the right amount of liquid.

To help clear up your infection completely, keep using this medicine for the full time of treatment, even if you begin to feel better after a few days. If you have a "strep'' infection, you should keep using this medicine for at least 10 days. This is especially important in "strep" infections. Serious heart problems could develop later if your infection is not cleared up completely. Also, if you stop taking this medicine too soon, your symptoms may return.

This medicine works best when there is a constant amount in the blood. To help keep the amount constant, do not miss any doses. Also, it is best to take each dose at evenly spaced times day and night. If you need help in planning the best times to take your medicine, check with your doctor.

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 forms (capsules and solution): For treatment of bacterial infections: Adults—150 to 300 milligrams (mg) every 6 hours. For more severe infections, 300 to 450 mg every 6 hours. Children weighing 10 kilograms (kg) or more—Dose is based on body weight and must be determined by your doctor. The dose is usually 8 to 16 milligrams (mg) per kilogram (kg) of body weight per day, divided into 3 or 4 equal doses. For more severe infections, the dose is usually 16 to 25 mg per kg of body weight per day, divided into 3 or 4 equal doses. Children weighing 10 kg or less—Dose is based on body weight and must be determined by your doctor. The dose is usually 37.5 milligrams (mg) or 1/2 teaspoonful 3 times a day.


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


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Detailed Antirobe Pediatric dosage information

Side effects

The most common side effects associated with Antirobe 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.


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

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Psychopathy and instrumental aggression: Evolutionary, neurobiological, and legal perspectives. The first half of the night was spent without CPAP and the second half with 10 cmH(2)O CPAP. NAFLD should be considered not only a liver specific disease but also an early mediator of systemic diseases. We assume that the functional responses that are usually included in such models are given by unspecified functions. Although kyphoplasty is associated with significant improvement of local kyphosis and less cement leakage, this does not result in long-term clinical and functional improvement. Retrospective study of cirrhotic patients with variceal UGIB, classified into 2 groups according to the development of AHH. Numbers of EF1A-haplotypes shared between mountain ranges correlate with geographical distance, suggesting relative isolation but occasional long-distance dispersal by spores. There were no significant changes in the systemic arterial pressure, arterial PO2 and PCO2 throughout the experiments in the two groups.

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The molecular mechanisms associated with the T-cell dysfunction remain to be elucidated. Cytoplasmic crystalloids are abundant in the excretory ducts of the accessory submandibular gland of the long-winged bat, Miniopterus magnator. The rarity of both conditions makes their association unlikely to be a chance event and an etiological relationship between them must be considered. Minisatellites include the most variable human loci described to date, and the mechanisms by which this safe dosage range protonix variation is generated in humans have been studied in detail. Neonatal fulminant type 2 infantile hepatic hemangioendothelioma involving skin, viscera and soft tissue. Functions of centromere protein B (CENP-B) and control of metaphase progression. Primary extraskeletal pleural osteosarcoma: a rare pleural identity.

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These data describe for the first time a direct effect of TH generic name of vantin through the T3Ralpha-receptor subtypes on postnatal intestinal mucosa maturation. Recent studies have suggested that gastroesophageal reflux disease (GERD) increases the risk of developing adenocarcinoma of the distal esophagus and cardia. In 14 female healthy volunteers, the activity of the pelvic floor was evaluated during a standardized horseback riding course by a biofeedback device. We identified seven children with atopic eczema who were known to have clinically significant latex allergy and examined the relationship of prior exposure to latex gloves. Invasive intraductal papillary-mucinous neoplasm of the pancreas: comparison with pancreatic ductal adenocarcinoma. Two crystal structures of recombinant Geobacillus stearothermophilus 6-phosphogluconate dehydrogenase (Gs6PDH) in complex with the substrate 6-phosphogluconate have been determined at medium resolution. The results from pharmacophore modeling and molecular docking are complementary to each other and could serve as a useful approach for the discovery of potent small molecules as p38 map kinase inhibitors. Antitumour effects of these schedules were also tested in C57BL/6N mice bearing Lewis lung carcinomas. Studies were conducted in which cells were pulse labeled for 30 min, followed by various periods of chase at 4 degrees C or 37 degrees C in the presence or absence of LDL receptor antibody. Phylogenetic and morphometric differentiation reveal geographic radiation and pseudo-cryptic speciation in a mangrove crab from the Indo-West Pacific.

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Symptomatic subjects received anesthetic infiltration of myofascial trigger points in the upper trapezius muscles and controls received the anesthetic in the thigh. Cartilage of the perichondriallly injured animals in the 8-week and 1(1/2)-year groups became histologically consistent with fibrous tissue. Five measures containing participation items linked to all 9 chapters were the Community Living Skills Scale, the Assessment of Life Habits, Mayo-Portland Adaptability Inventory, the participation measure for postacute care, and the Psychosocial Adjustment to Illness Scale. A questionnaire was sent to all members of the Japan Cornea Society requesting demographic and clinical findings on PMD patients who had been examined between 2008 and 2010. Data of 55 patients undergoing resurgery included clinicoradiological assessment and operative records. Japanese spotted fever: report of 31 cases and review of the literature. Thus health workforce policy, like other policies outside of health affairs, may be said, perhaps oversimply but not inaccurately, to have gone through three stages: from piety to platitudes to pork. The effect of home visits on the quality of life of children and adolescents with type 1 diabetes mellitus. Comparison of the indirect oscillometric and direct arterial methods for blood pressure measurements in anesthetized dogs. These findings may help to identify men at increased risk of acute urinary retention in whom closer evaluation may be warranted.

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Addressing the Appropriateness of Outpatient Antibiotic Prescribing in the United States: An Important First Step. Access to security spaces and the verification of credit cards require, ideally, a simple and inexpensive system that combines accuracy with a high resistance to compromise. Levels of cut-off values in the New-Criteria for younger adults were mostly between those of the Japanese-Criteria and recently established MetS-Criteria for adolescents. Symptoms abated after supportive therapy and discontinuation of prasugrel, the probable offending agent. Energy-dispersive X-ray spectroscopy showed the presence of the gold deposits in the cytoplasmic domain of the Kir receptor. The presence of non-Q-wave UMI predicts subsequent mortality, and is incremental to LVEF.

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