Cabergoline oral route
Cabergoline oral route
• Pleuro-pulmonary disease, such as dyspnoea, shortness of breath, persistent cough, or chest pain. The elimination half-life is estimated from urinary data of 12 healthy subjects to range between 63 to 69 hours. Cabergoline is usually taken twice each week for at least 6 months. Do not take this medicine every day unless your doctor tells you to. Follow all directions on your prescription label and read all medication guides or instruction sheets. Cabergoline is prescribed for a number of different medical conditions.
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Tell your health care provider if you are breastfeeding or plan to breastfeed. Your health care provider will let you know if you should stop breastfeeding or stop cabergoline. The most common side effects of cabergoline are listed below. Tell your health care provider if you have any of these side effects that bother you. It is important that your doctor does some tests every 6 to 12 months while you are taking Cabaser to make sure the medicine is working and to prevent unwanted side effects.
possible side effects
Cabergoline was also negative inthe bone marrow micronucleus test in the mouse. DOSTINEX Tablets are white, scored, capsule-shapedtablets containing 0.5 mg cabergoline. Each tablet is scored on one side andhas the letter P and the letter U on either side of the breakline. The otherside of the tablet is engraved with the number 700.
- Cabergoline may cause a sudden drop in blood pressure when standing up from a seated or lying position.
- Tell your health care provider if you have any of these side effects that bother you.
- Cabaser is intended for long-term use to prevent symptoms and complications of Parkinson’s.
- Cabaser may cause heart valve problems or may affect your lung and kidney function.
- Cabergoline should not be taken if you have or have had problems with your heart valves.
This medication belongs to a class of drugs called dopamine agonists which bind to dopamine receptors in cells and stimulate them. This increases the action of dopamine within the brain that helps to control movement of the body. Inaddition to the adverse events that occurred in the patients withhyperprolactinemic disorders, the most common adverse events in patients withParkinson’s disease were dyskinesia, hallucinations, confusion, and peripheraledema. Heart failure, pleural effusion, pulmonary fibrosis, and gastric or duodenal ulcer occurred rarely.
The prolactin-lowering action of cabergoline suggeststhat it will interfere with lactation. Due to this interference with lactation,DOSTINEX should not be given to women postpartum who are breastfeeding or whoare planning to breastfeed. The mutagenic potential of cabergoline was evaluated andfound to be negative in a battery of in https://newtonschools.sch.qa/uncategorized/halotestox-5-mg-p-b-labs-a-comprehensive-overview-3/ vitro tests.
Symptoms of overdose would likely be those of over-stimulation of dopamine receptors, e.g. nausea, vomiting, gastric complaints, postural hypotension, confusion/psychosis or hallucinations. In rats, cabergoline and/or its metabolites are excreted in milk. No information is available on excretion in breast milk in humans; however, lactation is expected to be inhibited/suppressed by cabergoline, in view of its dopamine agonist properties. Mothers should be advised not to breast-feed while being treated with cabergoline. Clinical diagnostic monitoring for development of fibrotic disorders, as appropriate, is essential. Serum creatinine measurements can also be used to help in the diagnosis of fibrotic disorder.