"The U.S. Food and Drug Administration today approved Clinolipid (lipid injectable emulsion, USP) for intravenous feeding (parenteral nutrition) in adult patients, providing a source of calories and essential fatty acids for adult patients who are"...
(Generic versions may still be available.)
The tuberculin skin test is based on the fact that mycobacterial infection produces delayed hypersensitivity to certain products of the organisms contained in culture extracts called tuberculins. The intracutaneous injection of tuberculin in sensitized individuals results in an area of induration, with or without surrounding erythema, which varies in size and intensity according to the dose of tuberculin and the sensitivity of the individual. This cell-mediated or delayed hypersensitivity reaction is characterized by its delayed course, reaching a peak at 48 to 72 hours, and by induration, due largely to cellular infiltration at the site of the antigen injection in sensitized persons called "reactors". Occasionally vesiculation and necrosis may occur. Not all reactors are infected with M. tuberculosis; infection with other species of mycobacteria may cause cross-reactions. The larger the reaction with a given antigenic dose, the greater is the probability that the reaction is specific for that antigen.
Last reviewed on RxList: 12/8/2004
This monograph has been modified to include the generic and brand name in many instances.
Additional Mono-Vacc Information
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Find out what women really need.