Does ALLANTOIN Cause Intentional product misuse? 73 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 73 reports of Intentional product misuse have been filed in association with ALLANTOIN (TriDerma Aloe Zinc Occlusive). This represents 46.5% of all adverse event reports for ALLANTOIN.
73
Reports of Intentional product misuse with ALLANTOIN
46.5%
of all ALLANTOIN reports
73
Deaths
67
Hospitalizations
How Dangerous Is Intentional product misuse From ALLANTOIN?
Of the 73 reports, 73 (100.0%) resulted in death, 67 (91.8%) required hospitalization, and 67 (91.8%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALLANTOIN. However, 73 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)
Off label use (99)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ALLANTOIN Alternatives Have Lower Intentional product misuse Risk?
ALLANTOIN vs ALLEGRA
ALLANTOIN vs ALLEGRA 24 HOUR
ALLANTOIN vs ALLEGRA D
ALLANTOIN vs ALLERGENIC EXTRACT- PEANUT ARACHIS HYPOGAEA
ALLANTOIN vs ALLERGENIC EXTRACTS