Does QUETIAPINE Cause Incorrect product administration duration? 41 Reports in FDA Database
Sharpen Your Memory & Focus Naturally
NeuroZoom — 35 clinically studied ingredients. No stimulants. Pure brain support.
According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Incorrect product administration duration have been filed in association with QUETIAPINE (Quetiapine). This represents 0.1% of all adverse event reports for QUETIAPINE.
41
Reports of Incorrect product administration duration with QUETIAPINE
0.1%
of all QUETIAPINE reports
3
Deaths
18
Hospitalizations
How Dangerous Is Incorrect product administration duration From QUETIAPINE?
Of the 41 reports, 3 (7.3%) resulted in death, 18 (43.9%) required hospitalization, and 13 (31.7%) 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 QUETIAPINE. However, 41 reports have been filed with the FAERS database.
What Other Side Effects Does QUETIAPINE Cause?
Toxicity to various agents (8,164)
Drug ineffective (5,707)
Off label use (5,296)
Completed suicide (4,997)
Somnolence (4,394)
Drug abuse (4,243)
Suicide attempt (4,060)
Intentional overdose (3,926)
Drug interaction (3,577)
Overdose (3,279)
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 QUETIAPINE Alternatives Have Lower Incorrect product administration duration Risk?
QUETIAPINE vs QUILLIVANT
QUETIAPINE vs QUINACRINE
QUETIAPINE vs QUINAPRIL
QUETIAPINE vs QUINAPRIL\QUINAPRIL
QUETIAPINE vs QUINIDINE