Riik: Iirimaa
keel: inglise
Allikas: HPRA (Health Products Regulatory Authority)
Conjugated estrogens
Pfizer Healthcare Ireland
G03CA; G03CA57
Conjugated estrogens
0.3 milligram(s)
Prolonged-release tablet
Product subject to prescription which may not be renewed (A)
Natural and semisynthetic estrogens, plain; conjugated estrogens
Not marketed
1988-07-25
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT PREMARIN ® 0.3 MG PROLONGED-RELEASE TABLETS (CONJUGATED OESTROGENS) READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. Keep this leaflet. You may need to read it again. If you have any further questions, ask your doctor, pharmacist or nurse. This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET 1. What Premarin is and what it is used for 2. What you need to know before you take Premarin 3. How to take Premarin 4. Possible side effects 5. How to store Premarin 6. Contents of the pack and other information 1. WHAT PREMARIN IS AND WHAT IT IS USED FOR Premarin is a Hormone Replacement Therapy (HRT). It contains the female hormone oestrogen. Premarin is used to treat some of the symptoms and conditions associated with the menopause. Premarin is usually prescribed for women who have had their womb removed (hysterectomy). However women who have not had this operation can still take Premarin and their doctor may prescribe a second type of tablet containing another hormone called a progestogen to be taken 12-14 days per month as well as the Premarin tablets. Premarin is used for: RELIEF OF SYMPTOMS OCCURRING AFTER MENOPAUSE During the menopause, the amount of the oestrogen produced by a woman’s body drops. This can cause symptoms such as hot face, neck and chest ("hot flushes"). Premarin alleviates these symptoms after menopause. You will only be prescribed Premarin if your symptoms seriously hinder your daily life. PREVENTION OF OSTEOPOROSIS After the menopause some women may be at risk of developing fragile bones (osteoporosis). You should discuss all available treatment options with your doctor. If you are at an incr Lugege kogu dokumenti
Health Products Regulatory Authority 10 January 2024 CRN00DZVQ Page 1 of 18 SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Premarin 0.3 mg Prolonged-release tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each tablet contains 0.3 mg conjugated oestrogens. Excipients with known effect: Each tablet contains lactose monohydrate 61.7 mg and sucrose 45.0 mg For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Prolonged-release tablet Green, oval, biconvex, coated tablets branded with “0.3” in white ink. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Premarin is indicated for hormone replacement therapy (HRT) for oestrogen deficiency symptoms in menopausal women and postmenopausal women. Prevention of osteoporosis in postmenopausal women at high risk of future fractures who are intolerant of, or contraindicated for, other medicinal products approved for the prevention of osteoporosis. (See section 4.4). 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Premarin is an oestrogen only HRTfor oral use. POSOLOGY _Adults_ Premarin 0.625-1.25 mg daily is the usual starting dose for women without a uterus. Continuous administration is recommended. For initiation and continuation of treatment of postmenopausal symptoms, the lowest effective dose for the shortest duration (see also section 4.4) should be used. Patients should be re-evaluated periodically to determine if treatment for symptoms is still necessary. Vasomotor symptoms: 0.625-1.25 mg daily depending on the response of the individual. Atrophic vaginitis, kraurosis vulvae, atrophic urethritis: 0.625-1.25 mg daily depending on the response of the individual. Health Products Regulatory Authority 10 January 2024 CRN00DZVQ Page 2 of 18 Prophylaxis of postmenopausal osteoporosis: When prescribing solely for the prevention of postmenopausal osteoporosis, therapy should only be considered for women at significant risk of osteoporosis and non-oestrogen medications should be carefully considered. The minimum effective dose is 0.625 mg f Lugege kogu dokumenti