Does ULMUS AMERICANA POLLEN Cause Off label use? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Off label use have been filed in association with ULMUS AMERICANA POLLEN (CENTER-AL - ULMUS AMERICANA POLLEN). This represents 7.6% of all adverse event reports for ULMUS AMERICANA POLLEN.
5
Reports of Off label use with ULMUS AMERICANA POLLEN
7.6%
of all ULMUS AMERICANA POLLEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Off label use From ULMUS AMERICANA POLLEN?
Of the 5 reports.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ULMUS AMERICANA POLLEN. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does ULMUS AMERICANA POLLEN Cause?
Anaphylactic reaction (19)
Injection site erythema (10)
Local reaction (9)
Urticaria (9)
Chest discomfort (7)
Injection site reaction (7)
Rash (7)
Dyspnoea (6)
Pruritus (6)
False negative investigation result (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)