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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does IODINE Cause Wrong technique in device usage process? 25 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Wrong technique in device usage process have been filed in association with IODINE (Iodine Tincture). This represents 1.4% of all adverse event reports for IODINE.

25
Reports of Wrong technique in device usage process with IODINE
1.4%
of all IODINE reports
0
Deaths
25
Hospitalizations

How Dangerous Is Wrong technique in device usage process From IODINE?

Of the 25 reports, 25 (100.0%) required hospitalization.

Is Wrong technique in device usage process Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for IODINE. However, 25 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 Wrong technique in device usage process?

ALBUTEROL (5,380) SOMATROPIN (4,746) EXENATIDE (3,255) FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673) FLUTICASONE\SALMETEROL (2,259) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197) INSULIN GLARGINE (1,749) UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531) BUDESONIDE\FORMOTEROL (1,481) BELIMUMAB (1,347)

Which IODINE Alternatives Have Lower Wrong technique in device usage process Risk?

IODINE vs IODINE\IOFLUPANE I-123 IODINE vs IODIXANOL IODINE vs IOHEXOL IODINE vs IOMEPROL IODINE vs IOPAMIDOL

Related Pages

IODINE Full Profile All Wrong technique in device usage process Reports All Drugs Causing Wrong technique in device usage process IODINE Demographics