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This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Read the entire detailed patient monograph for Dostinex (Cabergoline) SLIDESHOW. The safety of DOSTINEX Tablets has been evaluated in more than 900 patients with hyperprolactinemic disorders. Most adverse events were mild or moderate in severity, code promo superdry janvier 2021. In a 4-week, double-blind, placebo-controlled study, treatment consisted of placebo or cabergoline at fixed doses of 0. Doses were halved during the first week. Since a possible dose-related effect was observed for nausea only, the four cabergoline treatment groups have been combined. The incidence of the most common adverse events during the placebo-controlled study is presented in the following table. Incidence of Reported Adverse Events During the 4-Week, Double-Blind, Placebo- Controlled Trial Adverse Event* Cabergoline (n=168) 0. In the 8-week, double-blind period of the comparative trial with bromocriptine, DOSTINEX (at a dose of 0. The most common reasons for discontinuation from DOSTINEX were headache, nausea and vomiting (3, 2 and 2 patients respectively); the most common reasons for discontinuation from bromocriptine were nausea, vomiting, headache, and dizziness or vertigo (10, 3, 3, and 3 patients respectively). The incidence of the most common adverse events during the double-blind portion of the comparative trial with bromocriptine is presented in the following table. Incidence of Reported Adverse Events During the 8-Week, Double-Blind Period of the Comparative Trial With Bromocriptine Adverse Event* Cabergoline (n=221) Bromocriptine (n=231) Number (percent) Gastrointestinal Nausea 63 (29) 100 (43) Constipation 15 (7) 21 (9) Abdominal pain 12 (5) 19 (8) Dyspepsia 11 (5) 16 (7) Vomiting 9 (4) 16 (7) Dry mouth 5 (2) 2 (1) Diarrhea 4 (2) 7 (3) Flatulence 4 (2) 3 (1) Throat irritation 2 (1) 0 *Toothache 2 (1) 0 Central and Peripheral Nervous System Headache 58(26) 62(27) Dizziness 38(17) 42(18) Vertigo 9 (4) 10 (4) Paresthesia 5 (2) 6 (3) Body As a Whole Asthenia 13 (6) 15 (6) Fatigue 10 (5) 18 (8) Syncope 3 (1) 3 (1) Influenza-like symptoms 2 (1) 0 Malaise 2 (1) 0 Periorbital edema 2 (1) 2 (1) Peripheral edema 2 (1) 1 Psychiatric Depression 7 (3) 5 (2) Somnolence 5 (2) 5 (2) Anorexia 3 (1) 3 (1) Anxiety 3 (1) 3 (1) Insomnia 3 (1) 2 (1) Impaired concentration 2 (1) 1 Nervousness 2 (1) 5 (2) Cardiovascular Hot flashes 6 (3) 3 (1) Hypotension 3 (1) 4 (2) Dependent edema 2 (1) 1 Palpitation 2 (1) 5 (2) Reproductive – Female Breast pain 5 (2) 8 (3) Dysmenorrhea 2 (1) 1 Skin and Appendages Acne 3 (1) 0 Pruritus 2 (1) 1 Musculoskeletal Pain 4 (2) 6 (3) Arthralgia 2 (1) 0 Respiratory Rhinitis 2 (1) 9 (4) Vision Abnormal vision 2 (1) 2 (1) *Reported at ? 1% for cabergoline. Other adverse events that were reported at an incidence of. Manufactured by: Sun Pharmaceutical Industries Ltd Contains / Salt: Cabergoline (0. It is primarily used for the treatment of Acromegaly, Prolactinoma. The optimal dosage of Caberlin 0. The condition it has been prescribed for, and the route of administration also determine the right dosage. For detailed information on this, read through the dosage section. Some other side effects of Caberlin 0. These side effects of Caberlin 0. If, however, they worsen or do not go away, please speak with your physician. In addition, Caberlin 0.
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