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| Clinical data | |
|---|---|
| Trade names | Cabaser, Dostinex |
| AHFS/Drugs.com | Monograph |
| License data | US FDA: CABERGOLINE |
| Pregnancy category | US: B (No risk in non-human studies) |
| Routes of administration | Oral |
| ATC code | G02CB03 ( WHO ) N04BC06 ( WHO ) |
| Legal status | |
| Legal status | US: ℞-only |
| Pharmacokinetic data | |
| Bioavailability | First-pass effect seen; absolute bioavailability unknown |
| Protein binding | Moderately bound (40–42%); concentration-independent |
| Metabolism | Hepatic, predominately via hydrolysis of the acylurea bond or the urea moiety |
| Elimination half-life | 63–69 hours (estimated) |
| Excretion | Urine (22%), feces (60%) |
Available data do not indicate a special risk. Chest x-ray examination is recommended in cases of unexplained ESR increases to dostinex price uk values. In patients known to be intolerant to dopaminergic drugs, the likelihood of adverse events may be lessened by starting therapy with cabergoline at reduced doses, e.
Evidence of cardiac valvulopathy as determined by pre-treatment echocardiography. The maximum dose should not exceed 3mg per day.
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If you have uncontrolled high blood pressure or heart valve problems, you should not use this drug. Information for all health professionals If you are treating a patient who is taking cabergoline tablets marketed as Dostinex or Cabaser, advise them of this issue. If a patient returns a bottle of cabergoline Dostinex or Cabasertransfer the previously dispensed medicines into a new bottle with a child-resistant cap.
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Use in the elderly As a consequence of the indications for which cabergoline is presently proposed, the experience in elderly is very limited. Compared to normal volunteers and those with lesser degrees of hepatic insufficiency, an increase in AUC has been seen in patients with severe hepatic insufficiency Child-Pugh Class C who received a single 1 mg dose.
Treatment of hyperprolactinaemic disorders The recommended initial dosage of cabergoline is 0. The levitra buy cheap dosage is usually 1 mg per week and ranges from 0. Patients must be informed of this and dostinex price uk to exercise caution while driving or operating machines during treatment with cabergoline.
There is no information on perinatal disorders or long-term development of infants exposed to intra-uterine cabergoline.
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| Dostinex information | |
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| Drug name | dostinex |
| Active substance | cabergoline |
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Dostinex price uk and cardiac valvulopathy and possibly related clinical phenomena: Cabergoline should be discontinued if an echocardiogram reveals new or worsened valvular regurgitation, valvular restriction or valve leaflet thickening see section 4. Since decreases in blood pressure are frequently noted during the puerperium, independently of drug therapy, it is likely buy caverta 100mg many of the observed decreases in blood pressure after cabergoline administration were not drug-induced.
Furthermore a reduction in dosage or termination of therapy may be considered.
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In post-partum studies with cabergoline, blood pressure decreases were mostly asymptomatic and were frequently observed on a single occasion 2 to 4 days after treatment. As a precautionary measure, women who become pregnant should be monitored to detect signs of pituitary enlargement since expansion of pre-existing pituitary tumours may occur during gestation.
Care should be exercised when administering cabergoline concomitantly with other drugs known to lower blood pressure. Qualitative and quantitative composition One Dostinex tablet contains 0.
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Use in the elderly As a consequence of the indications for which cabergoline is presently proposed, the experience in elderly is very limited. No information is available about the interaction between cabergoline and other ergot alkaloids; therefore, the concomitant use of these medications during long-term treatment with cabergoline is not recommended.
Particular care should be taken when patients are taking concomitant psychoactive medication with tri.
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Pharmaceutical form Flat, capsule-shaped, 4 x 8 mm, scored, white tablets. The following undesirable effects have been observed and reported during treatment with cabergoline with the following frequencies: Clinical diagnostic monitoring for development of fibrotic disorders, as appropriate, is essential.
The weekly dose should be increased gradually, preferably by adding 0. Before cabergoline administration, pregnancy should be excluded and after treatment pregnancy should be prevented for at least one month.
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Before administration of cabergoline, pregnancy should be excluded. No information is available about the interaction between cabergoline and other ergot alkaloids; therefore, the concomitant use of these medications during long-term treatment with cabergoline is not recommended.
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In a twelve year observational study on pregnancy outcomes following cabergoline therapy, information is available on pregnancies. Excipients with known effect: Fibrotic and serosal inflammatory disorders such as pleuritis, pleural effusion, pleural fibrosis, pulmonary fibrosis, pericarditis, pericardial effusion, cardiac valvulopathy involving one or more valves aortic, mitral and tricuspid or retroperitoneal fibrosis have occurred after prolonged usage of ergot derivatives with agonist activity at the serotonin 5HT2B receptor, such as cabergoline.
Fibrotic disorders can have an insidious onset and patients should be regularly monitored for possible manifestations of progressive fibrosis. Pharmaceutical form Flat, capsule-shaped, 4 x 8 mm, scored, white tablets.
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