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After developmental toxicity was observed in animal research, the Food and Drug Administration within the United States requested the initiation of the Nuvigil/Provigil Pregnancy Registry to characterize the pregnancy and fetal outcomes related to Provigil (modafinil) and Nuvigil (armodafinil, the R-enantiomer of modafinil; not marketed in Canada) publicity during pregnancy. Using MODAFINIL shouldn't be allowed in persons who're allergic to any of its constituents present
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