Does SUFENTANIL Cause Suspected product quality issue? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Suspected product quality issue have been filed in association with SUFENTANIL (Sufentanil Citrate). This represents 0.5% of all adverse event reports for SUFENTANIL.
20
Reports of Suspected product quality issue with SUFENTANIL
0.5%
of all SUFENTANIL reports
0
Deaths
20
Hospitalizations
How Dangerous Is Suspected product quality issue From SUFENTANIL?
Of the 20 reports, 20 (100.0%) required hospitalization, and 20 (100.0%) 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 SUFENTANIL. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does SUFENTANIL Cause?
Anaphylactic shock (865)
Hypotension (403)
Anaphylactic reaction (257)
Drug ineffective (196)
Tachycardia (176)
Rash (134)
Cardiac arrest (128)
Off label use (126)
Rash maculo-papular (125)
Exposure during pregnancy (124)
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)
IOPROMIDE (25)
Which SUFENTANIL Alternatives Have Lower Suspected product quality issue Risk?
SUFENTANIL vs SUGAMMADEX
SUFENTANIL vs SULBACTAM
SUFENTANIL vs SULFACETAMIDE
SUFENTANIL vs SULFADIAZINE
SUFENTANIL vs SULFADIAZINE\TRIMETHOPRIM