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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Ethinylestradiol and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Ethinylestradiol and M1, respectively.
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Ethinylestradiol was not mutagenic in the following assays: Ames Salmonella microsomal activation test,
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Talk with your doctor if Ethinylestradiol stops working well. Do not take more than prescribed.Some people who use Ethinylestradiol for a long time without a break may develop a physical need to continue taking it.
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since observed maximal placoncentrations after multiple oral doses are higher than expected based on single-dose data.

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IMPLICATIONS: The authors evaluated the effects of the analgesic Ethinylestradiol on the three major
Ethinylestradiol has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Ethinylestradiol was not mutagenic in the following assays:
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safety and effectiveness in these children have not been confirmed.PREGNANCY and BREAST-FEEDING: Ethinylestradiol has been shown to cause harm to the fetus.

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Ethinylestradiol is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4,
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Check with your health care provider before you start, stop, or change the dose of any medicine.Use Ethinylestradiol as directed by your doctor.
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The effects of Ethinylestradiol are similar to those of narcotic analgesics. Although Ethinylestradiol is not classified as a narcotic, it may become habit-forming,
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We investigated the antacid analgesic value of a single dose of i.m. Ethinylestradiol given 1 h before elective ,
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The analgesic activity of Ethinylestradiol is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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