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Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Images Drug Interactions Compare Alternatives Pricing & Coupons En Espanol 88 Reviews Drug class: prolactin inhibitors. Advanced Reading Other brands Dostinex. Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. Copyright 1996-2021 Cerner Multum, Inc. You may need to read it again. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. This includes any possible side effects not listed in this leaflet. What is in this leaflet: 1) What Cabergoline is and what it is used for 2) What you need to know before you take Cabergoline 3) How to take Cabergoline 4) Possible side effects 5) How to store Cabergoline 6) Contents of the pack and other information. The effect of alcohol on the tolerability of cabergoline is unknown. Infertility can be reversed in women taking Cabergoline, and pregnancy can occur before the menstrual cycle has normalised. Suitable means of contraception should therefore be used during treatment if necessary, buy testocom 375 mg injectable steroids sustanon (testosterone blend). It is recommended that women on long term treatment with Cabergoline for hormonal disorders should have regular gynaecological exams including smear tests. Your doctor will continue to monitor your medical condition while you are taking Cabergoline tablets. Children and adolescents The safety and efficacy of Cabergoline has not been established in children and adolescents less than 16 years of age. Cabergoline can also be used to reduce abnormal quantities of the hormone prolactin in the blood. Other medicines and Cabergoline ‘ Certain medicines used for reducing blood pressure and certain medicinal products (e. The treating doctor should therefore be aware of such simultaneous medication. Tell your doctor or pharmacist if you are taking or have recently taken any other medicinal products, including those obtained without a prescription and natural medical products/natural products. Cabergoline with food and drink ‘ Cabergoline should be taken by mouth, preferably with meals. Cabergoline prevents lactation (production of milk) by decreasing levels of a hormone known as prolactin. Do not take Cabergoline if you: ‘ are allergic to cabergoline or other ergot alkaloids (e. Warnings and precautions If you have any of the following health problems you must inform your doctor before taking Cabergoline as the medicinal product may be unsuitable for you: ‘ cardiovascular disease ‘ stomach ulcer or bleeding in the gastrointestinal tract, (this condition can cause black faeces or vomiting with blood) ‘ impaired kidney function ‘ liver or kidney disease ‘ history of serious mental disease, particularly psychotic disorders ‘ Raynaud’s disease (when it is cold the fingers and toes become bluish white, with no pulse, cold, insensitive and numb) ‘ low blood pressure or you are taking medicines to lower blood pressure ‘ increased blood pressure after giving birth ‘ serious chest complaint (e. In case you are treated with Cabergoline for a long period, your doctor will check before starting treatment whether your heart, lungs and kidneys are in a good condition.
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Because clinical trials are conducted under widely varying conditions, adverse reactions rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Adjuvant Treatment of Early Breast Cancer. In study, BIG 1-98, the median treatment duration of adjuvant treatment was 60 months and the median duration of follow-up for safety was 96 months for patients receiving Femara and tamoxifen. Certain adverse reactions were prospectively specified for analysis (see Table 1), based on the known pharmacologic properties and side effect profiles of the two drugs. Adverse reactions were analyzed irrespective of whether a symptom was present or absent at baseline. Most adverse reactions reported (approximately 75% of patients who reported AEs) were Grade 1 or Grade 2 applying the Common Toxicity Criteria (CTC) Version 2. 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