Does ACETAMINOPHEN\CODEINE Cause Incorrect product administration duration? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Incorrect product administration duration have been filed in association with ACETAMINOPHEN\CODEINE. This represents 0.3% of all adverse event reports for ACETAMINOPHEN\CODEINE.
52
Reports of Incorrect product administration duration with ACETAMINOPHEN\CODEINE
0.3%
of all ACETAMINOPHEN\CODEINE reports
26
Deaths
43
Hospitalizations
How Dangerous Is Incorrect product administration duration From ACETAMINOPHEN\CODEINE?
Of the 52 reports, 26 (50.0%) resulted in death, 43 (82.7%) required hospitalization, and 42 (80.8%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\CODEINE. However, 52 reports have been filed with the FAERS database.
What Other Side Effects Does ACETAMINOPHEN\CODEINE Cause?
Dependence (3,857)
Overdose (2,600)
Pain (1,712)
Off label use (1,309)
Drug ineffective (1,300)
Nausea (1,291)
Drug dependence (1,273)
Fatigue (1,240)
Vomiting (1,224)
Depression (1,153)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ACETAMINOPHEN\CODEINE Alternatives Have Lower Incorrect product administration duration Risk?
ACETAMINOPHEN\CODEINE vs ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE
ACETAMINOPHEN\CODEINE vs ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE
ACETAMINOPHEN\CODEINE vs ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE\PHENYLEPHRINE
ACETAMINOPHEN\CODEINE vs ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN\PHENYLEPHRINE
ACETAMINOPHEN\CODEINE vs ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\PHENYLEPHRINE