Does IODINE Cause Product quality issue? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product quality issue have been filed in association with IODINE (Iodine Tincture). This represents 1.1% of all adverse event reports for IODINE.
20
Reports of Product quality issue with IODINE
1.1%
of all IODINE reports
18
Deaths
13
Hospitalizations
How Dangerous Is Product quality issue From IODINE?
Of the 20 reports, 18 (90.0%) resulted in death, 13 (65.0%) required hospitalization, and 19 (95.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IODINE. However, 20 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which IODINE Alternatives Have Lower Product quality issue Risk?
IODINE vs IODINE\IOFLUPANE I-123
IODINE vs IODIXANOL
IODINE vs IOHEXOL
IODINE vs IOMEPROL
IODINE vs IOPAMIDOL