Bayer Schering Pharma is proud to announce the availability of the first one tablet emergency contraceptive, Postinor®-X as of 1st September 2008. Postinor®-X contains 1.5mg of levonorgestrel and is indicated for use within 72 hours of unprotected intercourse. It should only be used as an emergency measure. Women who present for repeated courses of emergency contraception should seek advice to consider long-term methods of contraception.1 Postinor®-X’s convenient one tablet regimen eliminates confusion, and efficacy based on compliance to take a second tablet will no longer be a concern. Efficacy results also show, that the one tablet regimen appears to be more effective than the two tablet regimen taken twelve hours apart.1 With added benefits that accompany the one tablet, we anticipate that over time, Postinor®-X may replace all two tablet versions of the emergency contraceptive as the new gold standard. Both Healthcare Professionals and Consumers will be advised of the availability of Postinor®-X from 1st September 2008. You may therefore expect consumers to come in requesting a one tablet emergency contraceptive. We thus invite you to place your orders with wholesalers to ensure of availability. NB: Due to the introduction of Postinor-1, Postinor-2 will be phased out progressively until existing stock is exhausted. Yours faithfully Bayer Schering Pharma
Paul Tobolov Senior Product Manager Reference: 1. Approved Postinor-1 Product Information. Postinor-1 Dispensing Information Postinor-1: 1.5mg Levonorgestrel. Indications: Oral emergency contraception for use within 72 hours of unprotected intercourse. Women who present for repeated courses of emergency contraception should be advised to consider long-term methods of contraception. Contraindications: Should not be given to pregnant women or children. Unexplained vaginal bleeding, current breast cancer, hypersensitivity to any of the ingredients of the preparation. Precautions: Severe hypertension (BP>180+/110+), diabetes mellitus with nephropathy, retinopathy, neuropathy or vascular disease, ischaemic heart disease, stroke, or a past history of breast cancer. Severe hepatic dysfunction. Others: Refer to full Product Information. Interactions: Barbiturates, phenytoin, carbamazepine, herbal medicines containing hypericum perforatum (St John’s Wort), rifampicin, ritinovir, rifabutin, griseofulvin. Others: Refer to full Product Information. Adverse Events: Fatigue, nausea, vomiting, diarrhoea, abdominal pain, dizziness, headache, breast tenderness, menstrual disturbances. Others: Refer to full Product Information. Dosage: One 1.5mg tablet to be taken as soon as possible (and no later than 72 hours) after unprotected sex. PLEASE REVIEW PRODUCT INFORMATION BEFORE DISPENCING. Full Product Information is available on request from Bayer Australia Limited, ABN 22 000 138 714, 875 Pacific Highway, Pymble, NSW 2073.
Postinor-1 Support Material Fax Back Form
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DENOMINATION DU MEDICAMENT Myozyme® 50 mg poudre pour solution à diluer pour perfusion. 2. COMPOSITION QUALITATIVE ET QUANTITATIVE Un flacon contient 50 mg d’alpha alglucosidase. Après reconstitution, la solution contient 5 mg d’alpha alglucosidase* par ml et après dilution, la concentration varie de 0,5 mg à 4 mg/ml. *L’α-glucosidase acide humaine est produite par
Early release, published at www.cmaj.ca on December 3, 2012. Subject to revision. Risk of venous thromboembolism in women with polycystic ovary syndrome: a population-based matched cohort analysis Steven T. Bird PharmD MS, Abraham G. Hartzema PhD PharmD, James M. Brophy PhD MD, Mahyar Etminan PharmD MS, Joseph A.C. Delaney PhD Competing interests: Abraham Hartzema has Background: There