code L02BG04PubChem 3902DrugBank APRD01066Chemical dataFormula C17H11N5Mol. mass 285.303 g/molSMILES eMolecules & PubChemPharmacokinetic dataBioavailability 99.9%Protein binding 60%, mainly to albuminMetabolism ?Half life 2 daysExcretion ?Therapeutic considerationsPregnancy cat. ?Legal femara pregnancy ?(CA)Routes ?Letrozole.

breast cancerEstrogens are produced by the conversion of androgens through the activity of the growth plates in adolescents. This may boost the effectiveness of growth hormone, and thus Letrozole is used to treat endometriosis.[2][edit] References^ Tulandi T, Martin J, Al-Fadhli R, Kabli N, Forman R, Hitkari J, Librach C, Greenblatt E, femara pregnancy RF. Congenital malformations among 911 newborns conceived femara pregnancy infertility treatment with letrozole or clomiphene citrate. Fertil Steril. 2006 Apr 28. PMID 16650422^ femara pregnancy ESHRE abstract LetrozoleFrom Wikipedia, femara pregnancy free encyclopedia(Redirected from Femara)Jump to: navigation, searchLetrozoleSystematic (IUPAC) name4-[(4-cyanophenyl)-(1,2,4-triazol-1-yl)methyl]benzonitrileIdentifiersCAS number 112809-51-5ATC code L02BG04PubChem 3902DrugBank APRD01066Chemical dataFormula C17H11N5Mol. mass 285.303 g/molSMILES femara pregnancy & PubChemPharmacokinetic dataBioavailability 99.9%Protein binding 60%, femara pregnancy to femara pregnancy ?Half life 2 daysExcretion ?Therapeutic.

eMolecules & PubChemPharmacokinetic dataBioavailability 99.9%Protein binding 60%, mainly binding.