Does ALLANTOIN Cause Condition aggravated? 107 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 107 reports of Condition aggravated have been filed in association with ALLANTOIN (TriDerma Aloe Zinc Occlusive). This represents 68.2% of all adverse event reports for ALLANTOIN.
107
Reports of Condition aggravated with ALLANTOIN
68.2%
of all ALLANTOIN reports
104
Deaths
75
Hospitalizations
How Dangerous Is Condition aggravated From ALLANTOIN?
Of the 107 reports, 104 (97.2%) resulted in death, 75 (70.1%) required hospitalization, and 75 (70.1%) 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 ALLANTOIN. However, 107 reports have been filed with the FAERS database.
What Other Side Effects Does ALLANTOIN Cause?
Hyponatraemia (108)
General physical health deterioration (105)
Stress (105)
Multiple organ dysfunction syndrome (104)
Sepsis (103)
Somnolence (103)
Abdominal distension (101)
Vomiting (100)
Off label use (99)
Appendicitis (98)
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 ALLANTOIN Alternatives Have Lower Condition aggravated Risk?
ALLANTOIN vs ALLEGRA
ALLANTOIN vs ALLEGRA 24 HOUR
ALLANTOIN vs ALLEGRA D
ALLANTOIN vs ALLERGENIC EXTRACT- PEANUT ARACHIS HYPOGAEA
ALLANTOIN vs ALLERGENIC EXTRACTS