Does OXYCODONE Cause Incorrect product administration duration? 92 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Incorrect product administration duration have been filed in association with OXYCODONE (Oxycodone Hydrochloride). This represents 0.1% of all adverse event reports for OXYCODONE.
92
Reports of Incorrect product administration duration with OXYCODONE
0.1%
of all OXYCODONE reports
66
Deaths
69
Hospitalizations
How Dangerous Is Incorrect product administration duration From OXYCODONE?
Of the 92 reports, 66 (71.7%) resulted in death, 69 (75.0%) required hospitalization, and 56 (60.9%) 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 OXYCODONE. However, 92 reports have been filed with the FAERS database.
What Other Side Effects Does OXYCODONE Cause?
Drug dependence (104,927)
Pain (55,423)
Overdose (51,222)
Emotional distress (49,050)
Drug withdrawal syndrome (36,595)
Death (23,259)
Toxicity to various agents (17,518)
Drug abuse (11,835)
Drug ineffective (7,451)
Depression (6,871)
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 OXYCODONE Alternatives Have Lower Incorrect product administration duration Risk?
OXYCODONE vs OXYCODONE TEREPHTHALATE
OXYCODONE vs OXYCODONE\OXYCODONE
OXYCODONE vs OXYCONTIN
OXYCODONE vs OXYGEN
OXYCODONE vs OXYMETAZOLINE