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Empeea (Medroxyprogesterone)
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Empeea

Empeea is a progestin (female hormone). It works by replacing the natural progesterone hormone that the body is unable to make. This treats painful, irregular, or absent menstrual periods. It also prevents an overgrowth of the lining of the uterus in menopausal women taking estrogen (another female hormone).

Other names for this medication:
Curretab, Deviry, Empeea, Farlutal, Litmus, Medrigest, Medroxyprogesterone, Medtet, Megest, Megestone, Meprate, Orgamed, Parlutal, Premelle, Prodroxy, Regeeva, Remens, Sanigst, Topnid

Similar Products:
Antabuse, Diovan, Artane, Sustiva, Buspar, Angiofilina, Alertec, Etomax, Premarin, Atorlip, Amlonorm, Atekind, Aldbest, Metsina,

Also known as: Medroxyprogesterone

Description

Medroxyprogesterone is used to treat amenorrhea (unusual stopping of menstrual periods) and abnormal uterine bleeding. It is also used to prevent endometrial hyperplasia (thickening of the lining of the uterus or womb) in women who are taking conjugated estrogens. This medicine is a progestin hormone.

This medicine is available only with your doctor's prescription.

Dosage

Usual Adult Dose of depo-subQ Empeea 104 for Endometriosis:

104 mg subcutaneously once every 3 months (12 to 14 weeks) Duration of therapy: No longer than two years Comments: -For sexually active women having regular menses, the first injection should only be given within the first 5 days of a normal menstrual period or at 6 weeks postpartum, if the patient is breast feeding. -If the period between injections is more than 14 weeks, pregnancy should be ruled out prior to administering. -The impact of long-term use of the subcutaneous injection on bone mineral density (BMD) should be considered. -If symptoms return after discontinuation of treatment, BMD should be evaluated prior to retreatment. Use: Management of endometriosis-associated pain

Usual Adult Dose of Depo-Empeea for Contraception:

Intramuscular injection: -150 mg once every 3 months (13 weeks) in the gluteal or deltoid muscle Subcutaneous injection: -104 mg once every 3 months (12 to 14 weeks) into the anterior thigh or abdomen First injection: -Ensure the patient is not pregnant at the time of the first injection. -The first injection should be given only during the first 5 days of a normal menstrual period, within the first 5-days postpartum if not breast-feeding, and at the sixth postpartum week if breast-feeding. Switching from other methods of contraception: -IM injection: The first injection should be given on the day after the last active contraception tablet, or at the latest, on the day following the final inactive contraception tablet. -SC injection: The first injection should be given within 7 days after the last day taking the last active contraceptive tablet, or after removing the patch or ring. Similarly, contraceptive coverage will be maintained when switching from 150 mg IM injection, provided the next injection is given within the prescribed dosing period for the IM injection. Comments: -If the time interval between injections is greater than 13 weeks, pregnancy should be excluded before administering the drug. -The efficacy of the IM suspension depends on adherence to the dosage schedule of administration. -The risk/benefit of loss of bone mineral density (BMD) in women of all ages and the impact on peak bone mass in adolescents should be considered, along with the decrease in BMD that occurs during pregnancy and/or lactation, should be assessed when using this IM injection long-term. Use: Prevention of pregnancy in women of child bearing potential

Usual Pediatric Dose of Depo-Empeea for Contraception:

Postmenarchal children and adolescents: Intramuscular injection: -150 mg once every 3 months (13 weeks) in the gluteal or deltoid muscle Subcutaneous injection: -104 mg once every 3 months (12 to 14 weeks) into the anterior thigh or abdomen First injection: -Ensure the patient is not pregnant at the time of the first injection. -The first injection should be given only during the first 5 days of a normal menstrual period, within the first 5-days postpartum if not breast-feeding, and at the sixth postpartum week if breast-feeding. Switching from other methods of contraception: -IM injection: The first injection should be given on the day after the last active contraception tablet, or at the latest, on the day following the final inactive contraception tablet. -SC injection: The first injection should be given within 7 days after the last day taking the last active contraceptive tablet, or after removing the patch or ring. Similarly, contraceptive coverage will be maintained when switching from 150 mg IM injection, provided the next injection is given within the prescribed dosing period for the IM injection. Comments: -If the time interval between injections is greater than 13 weeks, pregnancy should be excluded before administering the drug. -The efficacy of the IM suspension depends on adherence to the dosage schedule of administration. -The risk/benefit of loss of bone mineral density (BMD) in women of all ages and the impact on peak bone mass in adolescents should be considered, along with the decrease in BMD that occurs during pregnancy and/or lactation, should be assessed when using the injection long-term. Use: Prevention of pregnancy in women of child bearing potential

Detailed Depo-Empeea dosage information

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Storage

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Detailed Empeea dosage information

Side effects

The most common side effects associated with Empeea are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Appropriate studies on the relationship of age to the effects of Depo-Empeea CI® (contraceptive injection) or Depo-Subq Empeea 104® have not been performed in the pediatric population. However, pediatric-specific problems that would limit the usefulness of this medicine in teenagers are not expected. This medicine may be used for birth control in teenage females, but should not be used before the start of menstruation.

Appropriate studies have not been performed on the relationship of age to the effects of Depo-Empeea® in the pediatric population. Safety and efficacy have not been established.

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Identity of the compound was confirmed by comparison of its retention time and relative intensity data with those of a standard or recovery from a fortified control liver sample. An instrument was developed in Canada to assess impairments related to oral functioning of individuals with four years of age or older with Down syndrome (DS). Effect of IGF-I and neurotrophin-3 on gracile neuroaxonal dystrophy in diabetic and aging rats. On the other hand, for a given cement formulation, vacuum mixing led to a statistically significant improvement in fatigue performance. Bike lanes can have a positive impact in creating a healthy neighborhood. The stability of IgY in the orogastrointestinal tract and its safety profile has been well-documented. But in Japan, the case of aortic dissection associated with bicuspid aortic valve is rare. Regional differences in the distribution of capsaicin-sensitive target-identified adult rat dorsal root ganglion neurons. All three methods were effective in reducing the need for homologous blood transfusions. PAI-RBP1 is a homolog of VIG, a part of the Drosophila melanogaster RNA-induced silencing complex (RISC).

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Presently, the cDNAs encoding for the 14-18-kDa proteins, designated the NZ-1 and NZ-2, respectively, and the 51-kDa protein, designated fertilization antigen, have been cloned and sequenced. Homologous recombination in Escherichia coli was used to generate a modified version of the BAC clone, in which an IRESbeta-geo cassette was inserted specifically into the Ren-1(d) gene. We performed a transcatheter arterial embolization and a subsequent CT angiography confirmed complete infarction of the sequestration. Inward and outward movement of flourescein across the human blood-retina barrier was studied in five healthy volunteers, using a differential spectrofluorometry method that eliminates the contribution of fluorescein glucuronide to the total fluorescence in the vitreous and in plasma. MCF7-Mdm2 cells showed a pronounced S-phase arrest after cisplatin treatment, similar to that observed in mutant-p53 cells in the present and prior studies. Effectiveness of training of basic health workers in Leprosy Control Programme.

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