POSTINOR is a brand name for Levonorgestrel. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Emergency contraception within 72 hours of unprotected sexual intercourse or failure of a contraceptive method. Postinor is indicated in adults and adolescents >16 years of age.
Verbatim from this product's MHRA label. Tap a section to expand.
1). e. e. 5). If vomiting occurs within three hours of taking the tablet, another tablet should be taken immediately. Postinor can be used at any time during the menstrual cycle unless menstrual bleeding is overdue. g. condom, diaphragm, spermicide, cervical cap) until the next menstrual period starts.
The use of levonorgestrel does not contraindicate the continuation of regular hormonal contraception. Paediatric population There is no relevant use of Postinor for children of prepubertal age in the indication emergency contraception Method of administration For oral administration.
The most commonly reported undesirable effect was nausea. Frequency of adverse reactions System Organ Class MedDRA Very common (≥1/10) Common ≥1/100 to <1/10) Nervous system disorders Headache Dizziness Gastrointestinal disorders Nausea Abdominal pain lower Diarrhoea Vomiting Reproductive system and breast disorders Bleeding not related to menses* Delay of menses more than 7 days ** Menstruation irregular Breast tenderness General disorders and administration site conditions Fatigue *Bleeding patterns may be temporarily disturbed, but most women will have their next menstrual period within 5-7 days of the expected time.
**If the next menstrual period is more than 5 days overdue, pregnancy should be excluded. From post-marketing surveillance additionally, the following adverse events have been reported: Gastrointestinal disorders Very rare (<1/10,000): abdominal pain Skin and subcutaneous tissue disorders Very rare (<1/10,000): rash, urticaria, pruritus, Reproductive system and breast disorders Very rare (<1/10,000): pelvic pain, dysmenorrhoea General disorders and administration site conditions Very rare (<1/10,000): face oedema Reporting of suspected adverse reactions: Reporting suspected adverse reactions after authorisation of the medicinal product is important.
It allows continued monitoring of the benefit/risk balance of the medicinal product. uk/yellowcard. By reporting side effects you can help provide more information on the safety of this medicine.
Emergency contraception is an occasional method. It should in no instance replace a regular contraceptive method. Emergency contraception does not prevent a pregnancy in every instance. If there is uncertainty about the timing of the unprotected intercourse or if the woman has had unprotected intercourse more than 72 hours earlier in the same menstrual cycle, conception may have occurred.
Treatment with levonorgestrel following the second act of intercourse may therefore be ineffective in preventing pregnancy. If menstrual periods are delayed by more than 5 days or abnormal bleeding occurs at the expected date of menstrual periods or pregnancy is suspected for any other reason, pregnancy should be excluded.
If pregnancy occurs after treatment with levonorgestrel, the possibility of an ectopic pregnancy should be considered. The absolute risk of ectopic pregnancy is likely to be low, as levonorgestrel prevents ovulation and fertilisation.
Ectopic pregnancy may continue, despite the occurrence of uterine bleeding. Therefore, levonorgestrel is not recommended for patients who are at risk of ectopic pregnancy (previous history of salpingitis or of ectopic pregnancy). Levonorgestrel is not recommended in patients with severe hepatic dysfunction.
Severe malabsorption syndromes, such as Crohn’s disease, might impair the efficacy of levonorgestrel. This medicinal product contains lactose monohydrate. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine.
After levonorgestrel intake, menstrual periods are usually normal and occur at the expected date. They can sometimes occur earlier or later than expected by a few days. Women should be advised to make a medical appointment to initiate or adopt a method of regular contraception.
If no withdrawal bleed occurs in the next pill-free period following the use of levonorgestrel after regular hormonal contraception, pregnancy should be ruled out. Repeated administration within a menstrual cycle is not advisable because of the possibility of disturbance of the cycle.
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Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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2). In all women, emergency contraception should be taken as soon as possible after unprotected intercourse, regardless of the woman’s body weight or BMI. Levonorgestrel is not as effective as a conventional regular method of contraception and is suitable only as an emergency measure.
Women who present for repeated courses of emergency contraception should be advised to consider long-term methods of contraception. Use of emergency contraception does not replace the necessary precautions against sexually transmitted diseases.