Does IODINE Cause Intentional product use issue? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Intentional product use issue have been filed in association with IODINE (Iodine Tincture). This represents 2.0% of all adverse event reports for IODINE.
35
Reports of Intentional product use issue with IODINE
2.0%
of all IODINE reports
32
Deaths
30
Hospitalizations
How Dangerous Is Intentional product use issue From IODINE?
Of the 35 reports, 32 (91.4%) resulted in death, 30 (85.7%) required hospitalization, and 33 (94.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IODINE. However, 35 reports have been filed with the FAERS database.
What Other Side Effects Does IODINE Cause?
Drug hypersensitivity (987)
Nausea (266)
Dyspnoea (259)
Fatigue (245)
Diarrhoea (229)
Arthralgia (225)
Headache (205)
Pruritus (201)
Vomiting (196)
Pyrexia (179)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which IODINE Alternatives Have Lower Intentional product use issue Risk?
IODINE vs IODINE\IOFLUPANE I-123
IODINE vs IODIXANOL
IODINE vs IOHEXOL
IODINE vs IOMEPROL
IODINE vs IOPAMIDOL