Does OPTIMARK Cause Nephrogenic systemic fibrosis? 121 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 121 reports of Nephrogenic systemic fibrosis have been filed in association with OPTIMARK. This represents 97.6% of all adverse event reports for OPTIMARK.
121
Reports of Nephrogenic systemic fibrosis with OPTIMARK
97.6%
of all OPTIMARK reports
15
Deaths
4
Hospitalizations
How Dangerous Is Nephrogenic systemic fibrosis From OPTIMARK?
Of the 121 reports, 15 (12.4%) resulted in death, 4 (3.3%) required hospitalization.
Is Nephrogenic systemic fibrosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OPTIMARK. However, 121 reports have been filed with the FAERS database.
What Other Side Effects Does OPTIMARK Cause?
What Other Drugs Cause Nephrogenic systemic fibrosis?
OMNISCAN (658)
GADOLINIUM (370)
MAGNEVIST (322)
GADODIAMIDE (99)
PROHANCE (85)
MULTIHANCE (77)
GADOPENTETATE DIMEGLUMINE (60)
GADOTERATE MEGLUMINE (36)
GADOBENATE DIMEGLUMINE (35)
GADOTERIDOL (31)
Which OPTIMARK Alternatives Have Lower Nephrogenic systemic fibrosis Risk?
OPTIMARK vs OPTIRAY
OPTIMARK vs ORELABRUTINIB
OPTIMARK vs ORENCIA
OPTIMARK vs ORITAVANCIN
OPTIMARK vs ORITAVANCIN DIPHOSPHATE