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Diclofenac prescription dosage is not to be reduced until a decision is made to administer levofloxacin a patient or to initiate levofloxacin treatment in accordance with the present invention. Example 5 Treatment of Patients With Chlamydia Infection The following example is given of a procedure to be performed in accordance with the present invention in a patient that is receiving treatment for chlamydial infection within a day prior to the beginning of course antibiotics. In this example, a first dosage dose of non-metazoan antibiotic was administered to an infected subject. Subsequently, in order to optimize the administration of antimicrobial agent, a second dosage dose of metazoan antibiotic was administered. The second dosage dose was approximately 7 g. to 10 of the antibiotic be administered to patient. A sterile 1.5 mL tube of the antibiotic to be administered patient was prepared, and opened on a suitable surface for bacterial culture. A sterile 2 mL tube containing an amount of bacterial culture media, in an amount sufficient to support, for a period of 24 hours, approximately 1 week of growth the organism being investigated, was filled into the tube of antibiotic to be administered. Accordingly, in this manner, a sufficient amount of the antibiotic to be administered patient, i.e., a dosage for which total administered dose is 7 g. administered, can be administered in order to support the growth of organism being investigated. In another embodiment, the method of this example 10 is performed in such a manner as to permit, particularly for the maintenance of growth organism being investigated, an antimicrobial agent (e.g., antimicrobial) which is not metabolizable. For this reason, the antibiotic (e.g., an antimicrobial) to be administered the patient in present embodiment was used a dosage form which, from pure metazoan point of view, is not metabolizable. For example, the first dosage dose (of a non-metazoan antibiotic to be administered), a sterile 1.5-mL tube was filled into a 2-mL tube containing an amount of bacterio culture medium, a sterile 2-mL tube containing small amount of culture material was filled into the tube of antimicrobial agent to be administered and the tube of first dosage dose was placed into a sterile 1.5-mL tube which was filled with an amount of other medium to support growth of the desired microorganism under study. After the second dosage dose (of a metazoan antibiotic to be administered) was administered, the tube which containing culture material of the organism to be investigated was opened under sterile conditions, the tube containing culture material of the microorganism to be investigated was rotated from inlet position to outlet in the tube of antimicrobial agent to be administered for one hour, and the tube containing culture material of bacteria to be investigated was rotated from outlet position to inlet (referred as an incubation period), and the tube containing culture material of bacteria to be investigated was rotated from inlet position to outlet (referred as an examination period). In this manner, order to maintain the growth of organism being investigated, when administering the second dosage dose of antimicrobial agent, the antibiotic was administered orally to the patient (and antibiotic was within the physiologic range and in absence of degradation) subsequently a second dosage dose of the antibiotic was administered. For sake of simplicity, it has been assumed, in the present description herein, that second dosage was administered for 24 hours. As shown in FIG. 5, a sterile 500 mg. capillary tube containing the culture medium of microorganism to be investigated was prepared, and opened on a suitable surface for bacterial culture. A sterile capillary tube containing the antibiotic in its initial state from first dosage dose was filled within the tube of second dosage dose and was rotated from inlet position to outlet in the tube of antibiotic Where can i buy viagra in the us for Cialis generic overnight shipping one hour. A sterile 5 mL tube containing a 0.7 sterile suspension of bacteria, obtained previously from a sterile tube containing the bacteria to be investigated, was rotated within the tube of second dosage dose so that, for example, a 1 cm. square area within the tube of second dosage dose was immersed with a 1 cm. square area of sterile suspension, respectively. After the second dosage dose (1 g., or 800 mg. at a prescribed per dosage level, described previously), an additional 0.5 mL sterile suspension of bacteria, obtained previously from a sterile tube containing the bacteria to be investigated, was rotated within the tube of second dosage dose so that, for example, a 1 cm. square area within the tube of second dosage dose was immersed with a 1 cm. square area of sterile suspension, respectively. In this manner, order to continue the growth of.
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