国: オーストラリア
言語: 英語
ソース: Department of Health (Therapeutic Goods Administration)
ethinylestradiol,levonorgestrel
Pfizer Australia Pty Ltd
ethinylestradiol,Levonorgestrel
Registered
NORDETTE ® _Levonorgestrel and Ethinylestradiol Tablets_ CONSUMER MEDICINE INFORMATION WHAT IS IN THIS LEAFLET This leaflet answers some common questions about Nordette. It does not contain all the available information. It does not take the place of talking to your doctor or pharmacist. All medicines have risks and benefits. Your doctor has weighed the risks of you taking Nordette against the benefits this medicine is expected to have for you. IF YOU HAVE ANY QUESTIONS ABOUT TAKING THIS MEDICINE, ASK YOUR DOCTOR OR PHARMACIST. KEEP THIS LEAFLET WITH THE MEDICINE. You may need to read it again. WHAT NORDETTE IS USED FOR Nordette is an oral contraceptive, commonly known as a "birth control pill" or "the Pill". Nordette tablets contain two hormones (levonorgestrel and ethinylestradiol), which prevent you from becoming pregnant if taken correctly. They are similar to the hormones that your body normally produces. Nordette prevents pregnancy in several ways: • It inhibits the egg release by stopping it maturing • It changes the cervical mucus consistency making it difficult for the sperm to reach the egg • It changes the lining of the uterus making it less suitable for implantation. ASK YOUR DOCTOR IF YOU HAVE ANY QUESTIONS ABOUT WHY NORDETTE HAS BEEN PRESCRIBED FOR YOU. Your doctor may have prescribed Nordette for another reason. This medicine is available only with a doctor's prescription. Nordette is not habit-forming. This medicine is not expected to affect your ability to drive a car or operate machinery. BEFORE YOU TAKE NORDETTE _WHEN YOU MUST NOT TAKE_ _NORDETTE_ DO NOT TAKE NORDETTE IF YOU HAVE AN ALLERGY TO: • ANY MEDICINE CONTAINING ETHINYLESTRADIOL OR LEVONORGESTREL • ANY OF THE INGREDIENTS LISTED AT THE END OF THIS LEAFLET • ANY OTHER SIMILAR MEDICINES (SUCH AS OTHER ORAL CONTRACEPTIVES). Some of the symptoms of an allergic reaction may include: • shortness of breath • wheezing or difficulty breathing • swelling of the face, lips, tongue or other parts of the body • rash, itching or h 完全なドキュメントを読む
Version: pfpnordt11219 Supersedes: pfpnordt11018 Page 1 of 25 AUSTRALIAN PRODUCT INFORMATION - NORDETTE (LEVONORGESTREL AND ETHINYLESTRADIOL) TABLETS 1. NAME OF THE MEDICINE Levonorgestrel and Ethinylestradiol 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each white tablet contains 30 micrograms of ethinylestradiol and 150 micrograms of levonorgestrel. Each red tablet contains no active ingredients. EXCIPIENTS WITH KNOWN EFFECT 1. Sucrose 2. Lactose monohydrate For the full list of excipients, see Section 6.1 - List of Excipients. 3. PHARMACEUTICAL FORM Tablet, sugar coated. Each blister contains 21 white tablets and 7 red tablets. White tablets: Shiny, smooth, sugar coated white tablets. Red tablets: Round, biconvex, sugar coated red inert tablets. 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS NORDETTE is indicated for the prevention of pregnancy. 4.2 DOSE AND METHOD OF ADMINISTRATION _HOW TO TAKE NORDETTE _ Each package of NORDETTE contains 21 white active tablets and 7 red inactive tablets. To achieve maximum contraceptive effectiveness, NORDETTE must be taken as directed and at intervals not exceeding 24 hours. Women should be instructed to take the tablets at the same time every day, preferably after the evening meal or at bedtime. Version: pfpnordt11219 Supersedes: pfpnordt11018 Page 2 of 25 _HOW TO START NORDETTE _ NO PRECEDING HORMONAL CONTRACEPTIVE USE (IN THE PAST MONTH) On the first day of the menstrual cycle, i.e. the first day of bleeding, the woman will take the first white active tablet corresponding to that day of the week from the green shaded section of the NORDETTE package. Thereafter, one white active tablet is taken daily, following the arrows on the package, until all 21 white active tablets have been taken. The woman should then be instructed to take one red inactive tablet from the light shaded section of the NORDETTE pack daily for the next seven days following the arrows marked. Withdrawal bleeding should usually occur within 3 days after the last white active tablet is taken and 完全なドキュメントを読む