Does IOPROMIDE Cause Suspected product quality issue? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Suspected product quality issue have been filed in association with IOPROMIDE (Ultravist). This represents 0.8% of all adverse event reports for IOPROMIDE.
25
Reports of Suspected product quality issue with IOPROMIDE
0.8%
of all IOPROMIDE reports
3
Deaths
14
Hospitalizations
How Dangerous Is Suspected product quality issue From IOPROMIDE?
Of the 25 reports, 3 (12.0%) resulted in death, 14 (56.0%) required hospitalization, and 3 (12.0%) were considered life-threatening.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IOPROMIDE. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does IOPROMIDE Cause?
Dyspnoea (473)
Urticaria (383)
Pruritus (358)
Anaphylactic shock (307)
Erythema (307)
Blood pressure decreased (306)
Nausea (245)
Vomiting (218)
Loss of consciousness (210)
Dizziness (186)
What Other Drugs Cause Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
PROPOFOL (25)
Which IOPROMIDE Alternatives Have Lower Suspected product quality issue Risk?
IOPROMIDE vs IOTHALAMIC ACID
IOPROMIDE vs IOVERSOL
IOPROMIDE vs IOXILAN
IOPROMIDE vs IPATASERTIB
IOPROMIDE vs IPILIMUMAB