Does IODINE\IOFLUPANE I-123 Cause Product quality issue? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product quality issue have been filed in association with IODINE\IOFLUPANE I-123. This represents 2.4% of all adverse event reports for IODINE\IOFLUPANE I-123.
11
Reports of Product quality issue with IODINE\IOFLUPANE I-123
2.4%
of all IODINE\IOFLUPANE I-123 reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From IODINE\IOFLUPANE I-123?
Of the 11 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IODINE\IOFLUPANE I-123. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does IODINE\IOFLUPANE I-123 Cause?
No adverse event (247)
Radioisotope scan abnormal (121)
Drug ineffective (101)
Injection site pain (58)
Drug interaction (31)
Burning sensation (23)
Parkinsonism (14)
False positive radioisotope investigation result (12)
Dizziness (8)
Nausea (8)
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\IOFLUPANE I-123 Alternatives Have Lower Product quality issue Risk?
IODINE\IOFLUPANE I-123 vs IODIXANOL
IODINE\IOFLUPANE I-123 vs IOHEXOL
IODINE\IOFLUPANE I-123 vs IOMEPROL
IODINE\IOFLUPANE I-123 vs IOPAMIDOL
IODINE\IOFLUPANE I-123 vs IOPROMIDE