Does OXYMETAZOLINE Cause Incorrect product administration duration? 118 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 118 reports of Incorrect product administration duration have been filed in association with OXYMETAZOLINE (Nasal). This represents 2.6% of all adverse event reports for OXYMETAZOLINE.
118
Reports of Incorrect product administration duration with OXYMETAZOLINE
2.6%
of all OXYMETAZOLINE reports
1
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product administration duration From OXYMETAZOLINE?
Of the 118 reports, 1 (0.8%) resulted in death, 4 (3.4%) required hospitalization, and 1 (0.8%) 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 OXYMETAZOLINE. However, 118 reports have been filed with the FAERS database.
What Other Side Effects Does OXYMETAZOLINE Cause?
Drug dependence (1,567)
Drug ineffective (486)
Vision blurred (261)
Product use issue (238)
Eye irritation (228)
Off label use (220)
Ocular hyperaemia (216)
Headache (200)
Anosmia (166)
Eye pain (144)
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 OXYMETAZOLINE Alternatives Have Lower Incorrect product administration duration Risk?
OXYMETAZOLINE vs OXYMORPHONE
OXYMETAZOLINE vs OXYQUINOLINE
OXYMETAZOLINE vs OXYTOCIN
OXYMETAZOLINE vs OXYTROL FOR WOMEN
OXYMETAZOLINE vs OZANIMOD