Esterified Estrogens and Methyltestosterone USA - engelsk - NLM (National Library of Medicine)

esterified estrogens and methyltestosterone

method pharmaceuticals, llc - estrogens, esterified (unii: 3asp8q3768) (estrogens, esterified - unii:3asp8q3768), methyltestosterone (unii: v9efu16zif) (methyltestosterone - unii:v9efu16zif) - estrogens, esterified 0.625 mg - esterified estrogens and methyltestosterone full strength and esterified estrogens and methyltestosterone half strength are indicated in the treatment of: moderate to severe vasomotor symptoms associated with the menopause in those patients not improved by estrogens alone. (there is no evidence that estrogens are effective for nervous symptoms or depression without associated vasomotor symptoms, and they should not be used to treat such conditions.) esterified estrogens and methyltestosterone full strength and esterified estrogens and methyltestosterone half strength have not been shown to be effective for any purpose during pregnancy and its use may cause severe harm to the fetus (see boxed warning). estrogens should not be used in women with any of the following conditions: 1.       known or suspected cancer of the breast except in appropriately selected patients being treated for metastatic disease. 2.       known or suspected estrogen-dependent ne

ESTERIFIED ESTROGENS AND METHYLTESTOSTERONE tablet USA - engelsk - NLM (National Library of Medicine)

esterified estrogens and methyltestosterone tablet

ani pharmaceuticals, inc. - estrogens, esterified (unii: 3asp8q3768) (estrogens, esterified - unii:3asp8q3768), methyltestosterone (unii: v9efu16zif) (methyltestosterone - unii:v9efu16zif) - estrogens, esterified 1.25 mg - esterified estrogens and methyltestosterone full and half-strength tablets are indicated in the: esterified estrogens and methyltestosterone full and half-strength tablets should not be used in women with any of the following conditions: methyltestosterone should not be used in: methyltestosterone is classified as a schedule iii controlled substance under the anabolic steroids act of 1990.

OVESTIN Israel - engelsk - Ministry of Health

ovestin

padagis israel agencies ltd, israel - estriol - cream - estriol 0.1 % - estriol - for the treatment of vulvo-vaginal complaints related to estrogen deficiency.

OGEN- estropipate cream USA - engelsk - NLM (National Library of Medicine)

ogen- estropipate cream

pharmacia and upjohn company - estropipate (unii: svi38uy019) (estropipate - unii:svi38uy019) - cream - 1.5 mg in 1 g - ogen vaginal cream is indicated for the treatment of vulval and vaginal atrophy. estrogens should not be used in individuals with any of the following conditions: - known or suspected pregnancy (see boxed warning ). estrogens may cause fetal harm when administered to a pregnant woman. - undiagnosed abnormal genital bleeding. - known or suspected cancer of the breast except in appropriately selected patients being treated for metastatic disease. - known or suspected estrogen-dependent neoplasia. - active thrombophlebitis or thromboembolic disorders. ogen vaginal cream (estropipate) is contraindicated in patients hypersensitive to its ingredients.

MONISTAT 7 VAGINAL CREAM Canada - engelsk - Health Canada

monistat 7 vaginal cream

insight pharmaceuticals, llc - miconazole nitrate - cream - 2% - miconazole nitrate 2% - azoles

MICONAZOLE NITRATE VAGINAL CREAM USP, 2% Canada - engelsk - Health Canada

miconazole nitrate vaginal cream usp, 2%

taro pharmaceuticals inc - miconazole nitrate - cream - 2% - miconazole nitrate 2% - azoles

MONISTAT 3 VAGINAL CREAM Canada - engelsk - Health Canada

monistat 3 vaginal cream

insight pharmaceuticals, llc - miconazole nitrate - cream - 4% - miconazole nitrate 4% - azoles

VESPEN estriol 1 mg/g cream tube Australia - engelsk - Department of Health (Therapeutic Goods Administration)

vespen estriol 1 mg/g cream tube

aspen pharmacare australia pty ltd - estriol, quantity: 1 mg/g - cream - excipient ingredients: sodium hydroxide; stearyl alcohol; lactic acid; cetyl esters wax; purified water; chlorhexidine hydrochloride; sorbitan monostearate; octyldodecanol; glycerol; polysorbate 60; cetyl alcohol - indication as at 6 july 2016: vulvo-vaginal complaints due to oestrogen deficiency associated with the climacteric and the postmenopause or after ovariectomy: ? atrophic vaginitis ? pruritus vulvae ? dyspareunia due to vulvo-vaginal atrophy ? as auxiliary therapy in the treatment of vaginal infections ? as pre-operative therapy for vulvo-vaginal surgery and during subsequent convalescence ? ulcers in cases of prolapse of the uterus or vagina ? to avoid misinterpretation of a cytological smear

PREMPRO- conjugated estrogens and medroxyprogesterone acetate tablet, sugar coated USA - engelsk - NLM (National Library of Medicine)

prempro- conjugated estrogens and medroxyprogesterone acetate tablet, sugar coated

dispensing solutions, inc. - estrogens, conjugated (unii: iu5qr144qx) (estrogens, conjugated - unii:iu5qr144qx), medroxyprogesterone acetate (unii: c2qi4ioi2g) (medroxyprogesterone - unii:hsu1c9yres) - estrogens, conjugated 0.3 mg - prempro or premphase therapy should not be used in women with any of the following conditions: - undiagnosed abnormal genital bleeding - known, suspected, or history of breast cancer - known or suspected estrogen-dependent neoplasia - active deep vein thrombosis, pulmonary embolism or a history of these conditions - active arterial thromboembolic disease (for example, stroke and myocardial infarction), or a history of these conditions - known liver dysfunction or disease - known thrombophilic disorders (e.g., protein c, protein s, or antithrombin deficiency) - known or suspected pregnancy prempro and premphase should not be used during pregnancy [see contraindications (4)] . there appears to be little or no increased risk of birth defects in children born to women who have used estrogens and progestins as an oral contraceptive inadvertently during early pregnancy. prempro and premphase should not be used during lactation. estrogen administration to nursing mothers has been shown to decrease the quanti

PREMPRO- conjugated estrogens and medroxyprogesterone acetate tablet, sugar coated USA - engelsk - NLM (National Library of Medicine)

prempro- conjugated estrogens and medroxyprogesterone acetate tablet, sugar coated

physicians total care, inc. - estrogens, conjugated (unii: iu5qr144qx) (estrogens, conjugated - unii:iu5qr144qx), medroxyprogesterone acetate (unii: c2qi4ioi2g) (medroxyprogesterone - unii:hsu1c9yres) - estrogens, conjugated 0.3 mg - prempro or premphase therapy should not be used in women with any of the following conditions: - undiagnosed abnormal genital bleeding - known, suspected, or history of breast cancer - known or suspected estrogen-dependent neoplasia - active deep vein thrombosis, pulmonary embolism or a history of these conditions - active arterial thromboembolic disease (for example, stroke and myocardial infarction), or a history of these conditions - known liver dysfunction or disease - known thrombophilic disorders (e.g., protein c, protein s, or antithrombin deficiency) - known or suspected pregnancy prempro and premphase should not be used during pregnancy [see contraindications (4)] . there appears to be little or no increased risk of birth defects in children born to women who have used estrogens and progestins as an oral contraceptive inadvertently during early pregnancy. prempro and premphase should not be used during lactation. estrogen administration to nursing mothers has been shown to decrease the quanti