CABERGOLINE for Blood prolactin increased: Side Effects & Safety Data
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There are 91 adverse event reports in the FDA FAERS database where CABERGOLINE was used for Blood prolactin increased.
Most Reported Side Effects for CABERGOLINE
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Drug ineffective | 249 | 11.9% | 5 | 50 |
| Headache | 142 | 6.8% | 7 | 28 |
| Off label use | 129 | 6.2% | 7 | 53 |
| Nausea | 103 | 4.9% | 1 | 20 |
| Maternal exposure during pregnancy | 100 | 4.8% | 9 | 16 |
| Dizziness | 94 | 4.5% | 1 | 17 |
| Cerebrospinal fluid leakage | 78 | 3.7% | 0 | 33 |
| Fatigue | 71 | 3.4% | 5 | 17 |
| Malaise | 64 | 3.1% | 1 | 17 |
| Condition aggravated | 61 | 2.9% | 1 | 25 |
| Product use in unapproved indication | 61 | 2.9% | 0 | 21 |
| Drug intolerance | 60 | 2.9% | 2 | 13 |
| Dyspnoea | 54 | 2.6% | 2 | 28 |
| Anxiety | 53 | 2.5% | 1 | 12 |
| Depression | 51 | 2.4% | 1 | 15 |
Other Indications for CABERGOLINE
Prolactin-producing pituitary tumour (481)
Pituitary tumour benign (208)
Product used for unknown indication (199)
Hyperprolactinaemia (169)
Acromegaly (87)
Pituitary tumour (84)
Lactation inhibition therapy (66)
Parkinson's disease (66)
Prolactinoma (53)
Pituitary-dependent cushing's syndrome (32)