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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 GADOLINIUM Cause Nephrogenic systemic fibrosis? 370 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 370 reports of Nephrogenic systemic fibrosis have been filed in association with GADOLINIUM (Gadolinium Metallicum). This represents 28.1% of all adverse event reports for GADOLINIUM.

370
Reports of Nephrogenic systemic fibrosis with GADOLINIUM
28.1%
of all GADOLINIUM reports
32
Deaths
8
Hospitalizations

How Dangerous Is Nephrogenic systemic fibrosis From GADOLINIUM?

Of the 370 reports, 32 (8.6%) resulted in death, 8 (2.2%) required hospitalization, and 2 (0.5%) were considered life-threatening.

Is Nephrogenic systemic fibrosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GADOLINIUM. However, 370 reports have been filed with the FAERS database.

What Other Side Effects Does GADOLINIUM Cause?

Gadolinium deposition disease (310) Pain (310) Arthralgia (303) Fatigue (278) Burning sensation (272) Paraesthesia (264) Hypoaesthesia (260) Asthenia (257) Rash (253) Muscle spasms (250)

What Other Drugs Cause Nephrogenic systemic fibrosis?

OMNISCAN (658) MAGNEVIST (322) OPTIMARK (121) GADODIAMIDE (99) PROHANCE (85) MULTIHANCE (77) GADOPENTETATE DIMEGLUMINE (60) GADOTERATE MEGLUMINE (36) GADOBENATE DIMEGLUMINE (35) GADOTERIDOL (31)

Which GADOLINIUM Alternatives Have Lower Nephrogenic systemic fibrosis Risk?

GADOLINIUM vs GADOPENTETATE DIMEGLUMINE GADOLINIUM vs GADOPICLENOL GADOLINIUM vs GADOTERATE MEGLUMINE GADOLINIUM vs GADOTERIDOL GADOLINIUM vs GADOVERSETAMIDE

Related Pages

GADOLINIUM Full Profile All Nephrogenic systemic fibrosis Reports All Drugs Causing Nephrogenic systemic fibrosis GADOLINIUM Demographics