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  1. DESCRIPTION. ORTHO EVRA® is a combination transdermal contraceptive patch with a contact surface area of 20 cm2. It contains 6.00 mg norelgestromin (NGMN) and 0.75 mg ethinyl estradiol (EE).

  2. 1. NAME OF THE MEDICINAL PRODUCT. EVRA 203 micrograms/24 hours + 33.9 micrograms/24 hours transdermal patch. 2. QUALITATIVE AND QUANTITATIVE COMPOSITION. Each 20 cm2 transdermal patch contains 6 mg norelgestromin (NGMN) and 600 micrograms ethinyl estradiol (EE).

  3. ORTHO EVRA® is a combination transdermal contraceptive patch with a contact surface area of 20 cm 2 .It contains 6.00 mg norelgestromin and 0.75 mg ethinyl estradiol (EE),and releases 150 micrograms of norelgestromin and 20 micrograms of EE to the bloodstream per 24 hours.

  4. FORMS, COMPOSITION AND PACKAGING section. INDICATIONS AND CLINICAL USE The EVRA® (norelgestromin and ethinyl estradiol) transdermal system is indicated for the prevention of pregnancy. The pharmacokinetic profile for the EVRA® transdermal system is different from that of an oral contraceptive.

  5. ACTIVE INGREDIENT(S): Norelgestromin (NGMN) and ethinyl estradiol (EE). o Summary of Product Characteristics (SmPC) before pre. embolism (VTE), and how the risk of VTE with EVRA. compares with other CHCs (see contraindications and special warn. Adults: Transdermal use. One patc. for 7 days, for 3 weeks followed by 1 week patch free. .

  6. What is in this leaflet. What EVRA is and what it is used for. What you need to know before you use EVRA. How to use EVRA. Possible side effects. How to store EVRA. Contents of the pack and other information. What EVRA is and what is it used for. ntains two types of sex hormones, a progestogen called norelgestromin and an oestrogen ca. c.

  7. ACTION AND CLINICAL PHARMACOLOGY. The EVRA (norelgestromin and ethinyl estradiol) transdermal system, with a contact surface area of 20 cm2, is a thin, matrix-type transdermal system consisting of three layers. Each transdermal system contains 6.0 mg norelgestromin and 0.60 mg ethinyl estradiol (EE).

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