Does NIVOLUMAB Cause Hyperprolactinaemia? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Hyperprolactinaemia have been filed in association with NIVOLUMAB (OPDIVO). This represents 0.0% of all adverse event reports for NIVOLUMAB.
9
Reports of Hyperprolactinaemia with NIVOLUMAB
0.0%
of all NIVOLUMAB reports
3
Deaths
5
Hospitalizations
How Dangerous Is Hyperprolactinaemia From NIVOLUMAB?
Of the 9 reports, 3 (33.3%) resulted in death, 5 (55.6%) required hospitalization.
Is Hyperprolactinaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NIVOLUMAB. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does NIVOLUMAB Cause?
Death (11,216)
Malignant neoplasm progression (9,363)
Off label use (5,208)
Diarrhoea (4,692)
Fatigue (3,709)
Pyrexia (3,454)
Intentional product use issue (3,297)
Rash (2,816)
Nausea (2,805)
Decreased appetite (2,619)
What Other Drugs Cause Hyperprolactinaemia?
RISPERIDONE (4,124)
PALIPERIDONE (1,427)
OLANZAPINE (520)
ARIPIPRAZOLE (459)
QUETIAPINE (331)
HALOPERIDOL (214)
CLOZAPINE (157)
AMISULPRIDE (135)
SERTRALINE (120)
LITHIUM (76)
Which NIVOLUMAB Alternatives Have Lower Hyperprolactinaemia Risk?
NIVOLUMAB vs NIVOLUMAB\RELATLIMAB-RMBW
NIVOLUMAB vs NIZATIDINE
NIVOLUMAB vs NOMEGESTROL
NIVOLUMAB vs NORDAZEPAM
NIVOLUMAB vs NOREPINEPHRINE