Does CABERGOLINE Cause Condition aggravated? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Condition aggravated have been filed in association with CABERGOLINE (Cabergoline). This represents 2.9% of all adverse event reports for CABERGOLINE.
61
Reports of Condition aggravated with CABERGOLINE
2.9%
of all CABERGOLINE reports
1
Deaths
25
Hospitalizations
How Dangerous Is Condition aggravated From CABERGOLINE?
Of the 61 reports, 1 (1.6%) resulted in death, 25 (41.0%) required hospitalization, and 6 (9.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABERGOLINE. However, 61 reports have been filed with the FAERS database.
What Other Side Effects Does CABERGOLINE Cause?
Drug ineffective (249)
Headache (142)
Off label use (129)
Nausea (103)
Maternal exposure during pregnancy (100)
Dizziness (94)
Cerebrospinal fluid leakage (78)
Fatigue (71)
Malaise (64)
Product use in unapproved indication (61)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CABERGOLINE Alternatives Have Lower Condition aggravated Risk?
CABERGOLINE vs CABOTEGRAVIR
CABERGOLINE vs CABOTEGRAVIR\RILPIVIRINE
CABERGOLINE vs CABOZANTINIB
CABERGOLINE vs CABOZANTINIB S-MALATE
CABERGOLINE vs CAFFEINE