Brand name: tetracycline
Generic name: Sumycin, Tetracyn, Terramycin, Panmycin

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A decrease in the fibula growth rate has been observed in prematures given oral tetracycline in doses of 25 mg/kg every six hours. Standardized procedures are based on a dilution method1,3 (broth or agar) or equivalent with standardized inoculum concentrations and standardized concentrations of tetracycline powder. The following adverse reactions have been observed in patients receiving tetracyclines. Range applicable only to tests performed by disk diffusion method using a 30-mcg tetracycline-class disk and using Mueller-Hinton agar with 5% defibrinated sheep blood and incubated in 5% CO2. TETRACYCLINE DRUGS, THEREFORE, SHOULD NOT BE USED IN THIS AGE GROUP, EXCEPT FOR ANTHRAX, INCLUDING INHALATIONAL ANTHRAX (POST-EXPOSURE), UNLESS OTHER DRUGS ARE NOT LIKELY TO BE EFFECTIVE OR ARE CONTRAINDICATED. Interpretative criteria applicable only to tests performed by disk diffusion method using a 30-mcg tetracycline-class disk and using GC agar base with 1% defined growth supplement. Adrenal gland hyperplasia has been observed in goats and rats treated with oxytetracycline. Patients apt to be exposed to direct sunlight or ultraviolet light should be advised that this reaction can occur with tetracycline drugs, and treatment should be discontinued at the first evidence of skin erythema. If any tetracycline is used during pregnancy or if the patient becomes pregnant while taking these drugs, the patient should be apprised of the potential hazard to the fetus. The tetracyclines, including doxycycline, have a similar antimicrobial spectrum of activity against a wide range of gram-positive and gram-negative microorganisms. The chemical designation of the light-yellow crystalline powder is alpha-6-deoxy-5-oxytetracycline.

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