Does POVIDONE-IODINE Cause Incorrect product administration duration? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product administration duration have been filed in association with POVIDONE-IODINE (Lights Povindone Iodine Swabstick). This represents 0.4% of all adverse event reports for POVIDONE-IODINE.
6
Reports of Incorrect product administration duration with POVIDONE-IODINE
0.4%
of all POVIDONE-IODINE reports
5
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From POVIDONE-IODINE?
Of the 6 reports, 5 (83.3%) resulted in death, 5 (83.3%) required hospitalization, and 5 (83.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POVIDONE-IODINE. However, 6 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which POVIDONE-IODINE Alternatives Have Lower Incorrect product administration duration Risk?
POVIDONE-IODINE vs PRABOTULINUMTOXINA-XVFS
POVIDONE-IODINE vs PRADAXA
POVIDONE-IODINE vs PRALATREXATE
POVIDONE-IODINE vs PRALSETINIB
POVIDONE-IODINE vs PRAMIPEXOLE