Does FENTANYL Cause Product dose omission? 194 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 194 reports of Product dose omission have been filed in association with FENTANYL (FENTANYL). This represents 0.2% of all adverse event reports for FENTANYL.
194
Reports of Product dose omission with FENTANYL
0.2%
of all FENTANYL reports
0
Deaths
21
Hospitalizations
How Dangerous Is Product dose omission From FENTANYL?
Of the 194 reports, 21 (10.8%) required hospitalization, and 2 (1.0%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FENTANYL. However, 194 reports have been filed with the FAERS database.
What Other Side Effects Does FENTANYL Cause?
Death (16,577)
Toxicity to various agents (15,546)
Overdose (12,762)
Drug abuse (12,390)
Drug dependence (7,970)
Drug ineffective (6,328)
Pain (5,820)
Product adhesion issue (4,541)
Dependence (4,358)
Drug withdrawal syndrome (3,206)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which FENTANYL Alternatives Have Lower Product dose omission Risk?
FENTANYL vs FENTANYL SYSTEM
FENTANYL vs FENTANYL\FENTANYL
FENTANYL vs FENTORA
FENTANYL vs FERRIC ANHYDROUS
FENTANYL vs FERRIC CARBOXYMALTOSE