Does TAPENTADOL Cause Product dose omission? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Product dose omission have been filed in association with TAPENTADOL (Nucynta). This represents 0.2% of all adverse event reports for TAPENTADOL.
49
Reports of Product dose omission with TAPENTADOL
0.2%
of all TAPENTADOL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission From TAPENTADOL?
Of the 49 reports, 1 (2.0%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAPENTADOL. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does TAPENTADOL Cause?
Death (11,560)
Toxicity to various agents (9,617)
Overdose (5,843)
Drug abuse (1,566)
Drug dependence (1,019)
Drug withdrawal syndrome neonatal (945)
Accidental overdose (693)
Drug ineffective (633)
Pain (436)
Nausea (434)
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 TAPENTADOL Alternatives Have Lower Product dose omission Risk?
TAPENTADOL vs TAPINAROF
TAPENTADOL vs TARCEVA
TAPENTADOL vs TARLATAMAB
TAPENTADOL vs TARLATAMAB-DLLE
TAPENTADOL vs TASIGNA