Does POVIDONE-IODINE Cause Condition aggravated? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Condition aggravated have been filed in association with POVIDONE-IODINE (Lights Povindone Iodine Swabstick). This represents 3.0% of all adverse event reports for POVIDONE-IODINE.
43
Reports of Condition aggravated with POVIDONE-IODINE
3.0%
of all POVIDONE-IODINE reports
37
Deaths
38
Hospitalizations
How Dangerous Is Condition aggravated From POVIDONE-IODINE?
Of the 43 reports, 37 (86.0%) resulted in death, 38 (88.4%) required hospitalization, and 37 (86.0%) 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 POVIDONE-IODINE. However, 43 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 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 POVIDONE-IODINE Alternatives Have Lower Condition aggravated Risk?
POVIDONE-IODINE vs PRABOTULINUMTOXINA-XVFS
POVIDONE-IODINE vs PRADAXA
POVIDONE-IODINE vs PRALATREXATE
POVIDONE-IODINE vs PRALSETINIB
POVIDONE-IODINE vs PRAMIPEXOLE