Human toxic data

For most chemicals, actual human toxicity data are not available or critical information on exposure is lacking, so toxicity data from studies conducted in laboratory animals are extrapolated to estimate the potential toxicity in humans. Such extrapolation requires experienced scientific judgment. The toxicity data from animal species most representative of humans in terms of pharmacodynamic and pharmacokinetic properties are used for determining AEGLs. If data are not available on the species that best represents humans, the data from the most sensitive animal species are used to set AEGLs. Uncertainty factors are commonly used when animal data are used to estimate minimal risk levels for humans. The magnitude of uncertainty factors depends on the quality of the animal data used to determine the no-observed-adverse-effect level (NOAEL) and the mode of action of the substance in question. When available, pharmocokinetic data on tissue doses are considered for interspecies extrapolation. 

Human toxicity data are limited to secondary citations. Because these citations provided no experimental details, they cannot be considered reliable. Deaths have occurred from aniline ingestion and skin absorption, but doses were unknown. Reviews of the older literature indicate that a concentration of 5 ppm was considered safe for daily exposures, concentrations of 7 to 53 ppm produced slight symptoms after several hours, a concentration of 40 to 53 ppm was tolerated for 6 h without distinct symptoms, a concentration of 130 ppm may be tolerated for 0.5 to 1 h without immediate or late sequalae, and 100 to 160 ppm was the maximum concentration that could be inhaled for 1 h without serious disturbance. In studies of accidents with unknown exposure concentrations, methemoglobin levels of up to 72% were measured. Recoveries occurred with a minimum of medical intervention following cessation of exposure. 

Human toxicity data for these nerve agents have not been published or have not been established. 

Human toxicity data for the Novichok series nerve agents have not been published or have not been established. However, available information indicates that under optimum conditions novichok agents are 5-10 times more toxic than nerve agent VX (C01-A016). 

Hartung (1994), and ATSDR (1997), report human toxicity data that appear to be based largely on pre-1920 animal data. 

Herbicides are designed to kill plants, not animals, and in general have lower mammalian toxicity than insecticides. Most herbicides interfere with plant hormones or enzymes that do not have any direct counterpart in animals. The most serious human health concerns have been related to contaminants of the primary chemical herbicide. There is an enormous amount of animal and some human toxicity data on 2,4-D and 2,4,5-T, but it now appears that much of this toxicity is caused by the contaminant TCDD. Military personnel exposed to Agent Orange, often contaminated with TCDD, reported birth defects, cancers, liver disease, and other illness. These concerns led to improvement in the manufacturing process to reduce TCDD contamination and ultimately to a reduction in use of 2,4-D herbicides. There is also concern that some herbicides may affect wildlife. For example, atrazine, a persistent herbicide, may adversely affect frogs. Persistence of herbicides may also... 

Need for Validation with Human Toxicity Data... 

Human toxicity data, especially the median lethal dose, is extrapolated from animals or from accidental poisoning, homicides and suicides. Extrapolations from animal data are educated estimates which consider the differences in species and building in a safety factor. If a lethal dose is 10 mg/kg in a rat and we consider a human to be 10 times more sensitive 1 mg/kg will have another 10-fold safety margin. Animal testing also involves using what may seem as ridiculous doses in order to cover the safety factor. To find a statistically valid effect which occurs once in one million subjects, several million animals would have to be used, which is exhorbitantly... 

TABLE 2-4 Human Toxicity Data, Experimental Exposure to Ammonia... 

TABLE 4 3 Human Toxicity Data, Exposure to CUorine... 

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