Does ALLANTOIN Cause Off label use? 99 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 99 reports of Off label use have been filed in association with ALLANTOIN (TriDerma Aloe Zinc Occlusive). This represents 63.1% of all adverse event reports for ALLANTOIN.
99
Reports of Off label use with ALLANTOIN
63.1%
of all ALLANTOIN reports
99
Deaths
73
Hospitalizations
How Dangerous Is Off label use From ALLANTOIN?
Of the 99 reports, 99 (100.0%) resulted in death, 73 (73.7%) required hospitalization, and 74 (74.7%) 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 ALLANTOIN. However, 99 reports have been filed with the FAERS database.
What Other Side Effects Does ALLANTOIN Cause?
Hyponatraemia (108)
Condition aggravated (107)
General physical health deterioration (105)
Stress (105)
Multiple organ dysfunction syndrome (104)
Sepsis (103)
Somnolence (103)
Abdominal distension (101)
Vomiting (100)
Appendicitis (98)
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 ALLANTOIN Alternatives Have Lower Off label use Risk?
ALLANTOIN vs ALLEGRA
ALLANTOIN vs ALLEGRA 24 HOUR
ALLANTOIN vs ALLEGRA D
ALLANTOIN vs ALLERGENIC EXTRACT- PEANUT ARACHIS HYPOGAEA
ALLANTOIN vs ALLERGENIC EXTRACTS