Does CABERGOLINE Cause Off label use? 129 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 129 reports of Off label use have been filed in association with CABERGOLINE (Cabergoline). This represents 6.2% of all adverse event reports for CABERGOLINE.
129
Reports of Off label use with CABERGOLINE
6.2%
of all CABERGOLINE reports
7
Deaths
53
Hospitalizations
How Dangerous Is Off label use From CABERGOLINE?
Of the 129 reports, 7 (5.4%) resulted in death, 53 (41.1%) required hospitalization, and 8 (6.2%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABERGOLINE. However, 129 reports have been filed with the FAERS database.
What Other Side Effects Does CABERGOLINE Cause?
Drug ineffective (249)
Headache (142)
Nausea (103)
Maternal exposure during pregnancy (100)
Dizziness (94)
Cerebrospinal fluid leakage (78)
Fatigue (71)
Malaise (64)
Condition aggravated (61)
Product use in unapproved indication (61)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which CABERGOLINE Alternatives Have Lower Off label use Risk?
CABERGOLINE vs CABOTEGRAVIR
CABERGOLINE vs CABOTEGRAVIR\RILPIVIRINE
CABERGOLINE vs CABOZANTINIB
CABERGOLINE vs CABOZANTINIB S-MALATE
CABERGOLINE vs CAFFEINE