A study of children exposed to medroxyprogesterone acetate with median observation periods of 14 - 16 years, indicated no incidence of adverse effects on physical growth, mental growth and development of general health status. The physician should be alert to the earliest manifestations of impaired liver function. Data sources include IBM Watson Micromedex (updated 2 Sep 2020), Cerner Multum™ (updated 1 Sep 2020), … {* mailingAddress_postalCode *} {* #userInformationForm *} 10 MG: ATC Code.
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Although there are insufficient data to quantify the risk to exposed female fetuses, some of these drugs induce mild virilization of the external genitalia of the female fetus. The attributable risk is low because such pregnancies are uncommon.A significant increase in incidence of polysyndactyly and chromosomal anomalies was observed among infants of users of DEPO-PROVERA, the former being most pronounced in women under 30 years of age. Please try again. If absorption properties between adult and infant are comparable, this amount would be too low to suppress pituitary function in the infant. In adolescent females, interpretation of BMD results should take into account patient age and skeletal maturity. Please try again. {* traditionalSignIn_signInButton *} Store upright at controlled room temperature 15° to 30°C. Provera: Medroxyprogesterone belongs to the family of medications known as progesterones. Your login attempt failed. {* traditionalRegistration_password *} The physician and woman should discuss the risks of pregnancy versus the risks to the child, if DEPO-PROVERA is used during lactation, to determine the most appropriate course of action for the individual woman. {* traditionalSignIn_emailAddress *} moon face and blood pressure elevation). Depo-Provera: Medroxyprogesterone acetate belongs to the class of medication known as progestogens.

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Patient age ranged from 16 years to 48 years (see As women continue to use DEPO-PROVERA, fewer experience irregular bleeding patterns and more experience amenorrhea. down the sink or in the toilet) or in household garbage. Thereafter, examinations should be performed at least once a year, or more frequently if indicated. Depo-Provera (medroxyprogesterone) is a member of the contraceptives drug class and is commonly used for Abnormal Uterine Bleeding, Amenorrhea, Birth Control, and others. The benefits of contraceptive options and their risks must be evaluated individually for each woman.Long-term, case-controlled surveillance of users of DEPO-PROVERA found slight or no increased overall risk of breast cancer and no overall increased risk of ovarian, liver, or cervical cancer and a prolonged, protective effect of reducing the risk of endometrial cancer in the population of users.The World Health Organization Study, a component of a pooled analysis, showed an increased RR of 2.19 (95% CI 1.23 to 3.89) of breast cancer associated with the use of DEPO-PROVERA in women whose first exposure to drug was within the previous 4 years and who were under 35 years of age.

Medroxyprogesterone acetate belongs to the class of medication known as This medication is usually started within the first 5 days after the onset of a normal menstrual period. MEDROXYPROGESTERONE ACETATE: Ingredient Strength. For Non-CA residents Links to other sites are provided as a convenience to the viewer, and should not be taken as an endorsement of the sites or an association with their owners. Your login attempt failed. {* traditionalSignIn_password *} {* traditionalSignIn_signInButton *} {* traditionalRegistration_passwordConfirm *} The mean number of injections per DEPO-PROVERA user was 9.3.

Use of DEPO-PROVERA was associated with a significant decline from baseline in BMD.Partway through the trial, drug administration was stopped (at 120 weeks).

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