Does SERENOA REPENS WHOLE Cause Off label use? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Off label use have been filed in association with SERENOA REPENS WHOLE. This represents 9.4% of all adverse event reports for SERENOA REPENS WHOLE.
6
Reports of Off label use with SERENOA REPENS WHOLE
9.4%
of all SERENOA REPENS WHOLE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Off label use From SERENOA REPENS WHOLE?
Of the 6 reports, 3 (50.0%) required hospitalization.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SERENOA REPENS WHOLE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does SERENOA REPENS WHOLE Cause?
Blood cholesterol increased (18)
Blood triglycerides increased (18)
Fatigue (18)
Hyperglycaemia (18)
Hypertension (18)
Overdose (14)
Treatment noncompliance (12)
Orthostatic hypotension (5)
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)