“…The route of administration (intraperitoneal, intravenous, or oral) has essentially no influence on the toxicity of these compounds (Witkin, 1956). The difference between the no-effect amount and alethal dosage of N-methylhydrazine is small in apes (Mäkinen et al, 1977), but there is a large variation in individual human tolerances as indieated by case his tori es (Franke et al, 1967). Calculated lethai dos es for children and human adults, based on reports of false morel intoxication, are 10 to 30 Ilg/g and 20 to 50 Ilg/g, respectively (Schmidlin-Meszaros, 1974.…”