Dimetapp Dm Cold And Cough (Colour Free) For Export 2mg + 5mg Elixir Filippinerna - engelska - FDA (Food And Drug Administration)

dimetapp dm cold and cough (colour free) for export 2mg + 5mg elixir

wyeth consumer healthcare pty ltd - australia - brompheniramine maleate , phenylpherine hydrochloride - elixir - 2mg + 5mg

ESTRADERM MX 75 estradiol 75 microgram/24hr transdermal drug delivery system sachet Australien - engelska - Department of Health (Therapeutic Goods Administration)

estraderm mx 75 estradiol 75 microgram/24hr transdermal drug delivery system sachet

juno pharmaceuticals pty ltd - estradiol hemihydrate, quantity: 2.32 mg (equivalent: estradiol, qty 2.25 mg) - drug delivery system, transdermal - excipient ingredients: polyethylene terephthalate; isopropyl palmitate; ethyl acetate; acrylic acid; 2-ethylhexyl acrylate; methyl acrylate; glycidyl methacrylate; 2,2'-azobisisobutyronitrile; hexane - menopausal symptoms: short-term treatment of signs and symptoms of oestrogen deficiency due to menopause, whether natural or surgically induced. in women with an intact uterus, oestrogen should always be opposed by progestogen in an adequate dosage regimen to ensure secretory transformation of the endometrium at regular intervals (refer to section 5.1 pharmacodynamic properties - clinical trials and section 4.2 dose and method of administration). prevention of post-menopausal bone mineral density loss: estraderm mx 50, 75 and 100 may be used for prevention of post-menopausal bone mineral density loss in women with an increased risk of future osteoporotic fractures who are intolerant of, or contraindicated for, other medicinal products approved for the prevention of bone mineral density loss. when prescribed solely for the prevention of postmenopausal bone mineral density loss, therapy should only be prescribed for women who are at high risk of future fracture and who are intolerant of, or contraindicated for, non-oestrogen products approved for prevention of bone mineral density loss. lifestyle modifications and the risk-benefit profile of estraderm mx should be taken into careful consideration and discussed with the patient to allow the patient to make an informed decision prior to prescribing (see section 4.4 special warnings and precautions for use and section 4.2 dose and method of administration). combination hrt should not be used in hysterectomised women because it is not needed in these women and it may increase risk of breast cancer.

ESTRADERM MX 100 estradiol 100 microgram/24 hours transdermal drug delivery system sachet Australien - engelska - Department of Health (Therapeutic Goods Administration)

estraderm mx 100 estradiol 100 microgram/24 hours transdermal drug delivery system sachet

juno pharmaceuticals pty ltd - estradiol hemihydrate, quantity: 3.09 mg (equivalent: estradiol, qty 3 mg) - drug delivery system, transdermal - excipient ingredients: isopropyl palmitate; polyethylene terephthalate; ethyl acetate; acrylic acid; 2-ethylhexyl acrylate; methyl acrylate; glycidyl methacrylate; 2,2'-azobisisobutyronitrile; hexane - menopausal symptoms: short-term treatment of signs and symptoms of oestrogen deficiency due to menopause, whether natural or surgically induced. in women with an intact uterus, oestrogen should always be opposed by progestogen in an adequate dosage regimen to ensure secretory transformation of the endometrium at regular intervals (refer to section 5.1 pharmacodynamic properties - clinical trials and section 4.2 dose and method of administration). prevention of post-menopausal bone mineral density loss: estraderm mx 50, 75 and 100 may be used for prevention of post-menopausal bone mineral density loss in women with an increased risk of future osteoporotic fractures who are intolerant of, or contraindicated for, other medicinal products approved for the prevention of bone mineral density loss. when prescribed solely for the prevention of postmenopausal bone mineral density loss, therapy should only be prescribed for women who are at high risk of future fracture and who are intolerant of, or contraindicated for, non-oestrogen products approved for prevention of bone mineral density loss. lifestyle modifications and the risk-benefit profile of estraderm mx should be taken into careful consideration and discussed with the patient to allow the patient to make an informed decision prior to prescribing( see section 4.4 special warnings and precautions for use and section 4.2 dose and method of administration). combination hrt should not be used in hysterectomised women because it is not needed in these women and it may increase risk of breast cancer.

ESTRADERM MX 25 estradiol 25 microgram/24 hours transdermal drug delivery system sachet Australien - engelska - Department of Health (Therapeutic Goods Administration)

estraderm mx 25 estradiol 25 microgram/24 hours transdermal drug delivery system sachet

juno pharmaceuticals pty ltd - estradiol hemihydrate, quantity: 0.77 mg (equivalent: estradiol, qty 0.75 mg) - drug delivery system, transdermal - excipient ingredients: isopropyl palmitate; polyethylene terephthalate; ethyl acetate; acrylic acid; 2-ethylhexyl acrylate; methyl acrylate; glycidyl methacrylate; 2,2'-azobisisobutyronitrile; hexane - menopausal symptoms: short-term treatment of signs and symptoms of oestrogen deficiency due to menopause, whether natural or surgically induced. in women with an intact uterus, oestrogen should always be opposed by progestogen in an adequate dosage regimen to ensure secretory transformation of the endometrium at regular intervals (refer to section 5.1 pharmacodynamic properties - clinical trials and section 4.2 dose and method of administration). estraderm mx 25 is not indicated for the prevention of post-menopausal bone mineral density loss. combination hrt should not be used in hysterectomised women because it is not needed in these women and it may increase risk of breast cancer

ESTRADERM MX 50 estradiol 50 microgram/24 hours transdermal drug delivery system sachet Australien - engelska - Department of Health (Therapeutic Goods Administration)

estraderm mx 50 estradiol 50 microgram/24 hours transdermal drug delivery system sachet

juno pharmaceuticals pty ltd - estradiol hemihydrate, quantity: 1.54 mg (equivalent: estradiol, qty 1.5 mg) - drug delivery system, transdermal - excipient ingredients: isopropyl palmitate; polyethylene terephthalate; ethyl acetate; acrylic acid; 2-ethylhexyl acrylate; methyl acrylate; glycidyl methacrylate; 2,2'-azobisisobutyronitrile; hexane - menopausal symptoms: short-term treatment of signs and symptoms of oestrogen deficiency due to menopause, whether natural or surgically induced. in women with an intact uterus, oestrogen should always be opposed by progestogen in an adequate dosage regimen to ensure secretory transformation of the endometrium at regular intervals (refer to section 5.1 pharmacodynamic properties - clinical trials and section 4.2 dose and method of administration). prevention of post-menopausal bone mineral density loss: estraderm mx 50, 75 and 100 may be used for prevention of post-menopausal bone mineral density loss in women with an increased risk of future osteoporotic fractures who are intolerant of, or contraindicated for, other medicinal products approved for the prevention of bone mineral density loss. when prescribed solely for the prevention of postmenopausal bone mineral density loss, therapy should only be prescribed for women who are at high risk of future fracture and who are intolerant of, or contraindicated for, non-oestrogen products approved for prevention of bone mineral density loss. lifestyle modifications and the risk-benefit profile of estraderm mx should be taken into careful consideration and discussed with the patient to allow the patient to make an informed decision prior to prescribing (see section 4.4 special warnings and precautions for use and sectoin 4.2 dose and method of administration). combination hrt should not be used in hysterectomised women because it is not needed in these women and it may increase risk of breast cancer.

DIMETAPP 2mg+5mg / 5 mL Syrup Filippinerna - engelska - FDA (Food And Drug Administration)

dimetapp 2mg+5mg / 5 ml syrup

wyeth consumer healthcare pty limited - australia - brompheniramine maleate , phenylephrine hydrochloride - syrup - 2mg+5mg / 5 ml

Dimetapp DM Cold & Cough Elixir (Colour Free) [For Export Only] 2mg/ 5mg/ 10mg Elixir Filippinerna - engelska - FDA (Food And Drug Administration)

dimetapp dm cold & cough elixir (colour free) [for export only] 2mg/ 5mg/ 10mg elixir

wyeth consumer healthcare pty. ltd. - bromphrniramine maleate , phenylephrine hydrochloride , dextromethorphan hydrobromide - elixir - 2mg/ 5mg/ 10mg

Robitussin DX (For Export Only) 30mg/ 10mL Syrup Filippinerna - engelska - FDA (Food And Drug Administration)

robitussin dx (for export only) 30mg/ 10ml syrup

wyeth consumer healthcare pty. ltd. - dextromethorphan hydrobromide - syrup - 30mg/ 10ml

Donnatab (for Export Only) 103.7mcg/ 19.4mcg/ 6.5mcg Tablet Filippinerna - engelska - FDA (Food And Drug Administration)

donnatab (for export only) 103.7mcg/ 19.4mcg/ 6.5mcg tablet

wyeth consumer healthcare pty. ltd. - hyoscyamine sulfate , atropine sulfate , hyoscine hydrobromide - tablet - 103.7mcg/ 19.4mcg/ 6.5mcg