Does POVIDONE-IODINE Cause Intentional product use issue? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Intentional product use issue have been filed in association with POVIDONE-IODINE (Lights Povindone Iodine Swabstick). This represents 3.5% of all adverse event reports for POVIDONE-IODINE.
50
Reports of Intentional product use issue with POVIDONE-IODINE
3.5%
of all POVIDONE-IODINE reports
48
Deaths
46
Hospitalizations
How Dangerous Is Intentional product use issue From POVIDONE-IODINE?
Of the 50 reports, 48 (96.0%) resulted in death, 46 (92.0%) required hospitalization, and 48 (96.0%) 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 POVIDONE-IODINE. However, 50 reports have been filed with the FAERS database.
What Other Side Effects Does POVIDONE-IODINE Cause?
Drug hypersensitivity (307)
Rash (151)
Toxic anterior segment syndrome (144)
Drug ineffective (131)
Off label use (121)
Nausea (118)
Hypersensitivity (111)
Pain (110)
Endophthalmitis (104)
Eye pain (96)
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 POVIDONE-IODINE Alternatives Have Lower Intentional product use issue Risk?
POVIDONE-IODINE vs PRABOTULINUMTOXINA-XVFS
POVIDONE-IODINE vs PRADAXA
POVIDONE-IODINE vs PRALATREXATE
POVIDONE-IODINE vs PRALSETINIB
POVIDONE-IODINE vs PRAMIPEXOLE