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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.

IODIPAMIDE MEGLUMINE: 38 Adverse Event Reports & Safety Profile

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38
Total FAERS Reports
37 (97.4%)
Deaths Reported
38
Hospitalizations
38
As Primary/Secondary Suspect
37
Life-Threatening
37
Disabilities
Approved Prior to Jan 1, 1982
FDA Approved
Discontinued
Status

FDA Application: 009321 ·

First Report: 20100517 · Latest Report: 20150818

What Are the Most Common IODIPAMIDE MEGLUMINE Side Effects?

#1 Most Reported
Off label use
34 reports (89.5%)
#2 Most Reported
Hypercholesterolaemia
31 reports (81.6%)
#3 Most Reported
Duodenal ulcer perforation
31 reports (81.6%)

All IODIPAMIDE MEGLUMINE Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Off label use 34 89.5% 34 34
Duodenal ulcer perforation 31 81.6% 31 31
Hypercholesterolaemia 31 81.6% 31 31
Blepharospasm 30 79.0% 30 30
Depression 30 79.0% 30 30
Epilepsy 30 79.0% 30 30
Fibromyalgia 30 79.0% 30 30
Helicobacter infection 30 79.0% 30 30
Breast cancer stage iii 29 76.3% 29 29
Dry mouth 29 76.3% 29 29
Abdominal pain upper 28 73.7% 28 28
Asthenia 28 73.7% 28 28
Diarrhoea 28 73.7% 28 28
Facet joint syndrome 28 73.7% 28 28
Blister 27 71.1% 27 27
Dizziness 27 71.1% 27 27
Vomiting 27 71.1% 27 27
Hypertension 25 65.8% 25 25
Back injury 24 63.2% 24 24
Hypersensitivity 23 60.5% 23 23

Who Reports IODIPAMIDE MEGLUMINE Side Effects? Age & Gender Data

Gender: 98.0% female, 2.0% male. Average age: 40.5 years. Most reports from: CA. View detailed demographics →

Is IODIPAMIDE MEGLUMINE Getting Safer? Reports by Year

YearReportsDeathsHosp.
2010 1 0 1
2015 3 3 3

View full timeline →

What Is IODIPAMIDE MEGLUMINE Used For?

IndicationReports
Product used for unknown indication 33

Official FDA Label for IODIPAMIDE MEGLUMINE

Official prescribing information from the FDA-approved drug label.