Does CETIRIZINE Cause Incorrect product administration duration? 137 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 137 reports of Incorrect product administration duration have been filed in association with CETIRIZINE (Cetirizine). This represents 0.3% of all adverse event reports for CETIRIZINE.
137
Reports of Incorrect product administration duration with CETIRIZINE
0.3%
of all CETIRIZINE reports
69
Deaths
100
Hospitalizations
How Dangerous Is Incorrect product administration duration From CETIRIZINE?
Of the 137 reports, 69 (50.4%) resulted in death, 100 (73.0%) required hospitalization, and 77 (56.2%) 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 CETIRIZINE. However, 137 reports have been filed with the FAERS database.
What Other Side Effects Does CETIRIZINE Cause?
Drug ineffective (13,819)
Fatigue (9,476)
Pain (9,377)
Abdominal discomfort (8,413)
Alopecia (8,412)
Systemic lupus erythematosus (8,196)
Pemphigus (8,063)
Rheumatoid arthritis (7,891)
Off label use (7,790)
Glossodynia (7,407)
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 CETIRIZINE Alternatives Have Lower Incorrect product administration duration Risk?
CETIRIZINE vs CETIRIZINE\PSEUDOEPHEDRINE
CETIRIZINE vs CETRIMIDE
CETIRIZINE vs CETRORELIX
CETIRIZINE vs CETUXIMAB
CETIRIZINE vs CETYLPYRIDINIUM