Does QUETIAPINE Cause Product prescribing error? 203 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), 203 reports of Product prescribing error have been filed in association with QUETIAPINE (Quetiapine). This represents 0.3% of all adverse event reports for QUETIAPINE.
203
Reports of Product prescribing error with QUETIAPINE
0.3%
of all QUETIAPINE reports
13
Deaths
120
Hospitalizations
How Dangerous Is Product prescribing error From QUETIAPINE?
Of the 203 reports, 13 (6.4%) resulted in death, 120 (59.1%) required hospitalization, and 27 (13.3%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for QUETIAPINE. However, 203 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which QUETIAPINE Alternatives Have Lower Product prescribing error Risk?
QUETIAPINE vs QUILLIVANT
QUETIAPINE vs QUINACRINE
QUETIAPINE vs QUINAPRIL
QUETIAPINE vs QUINAPRIL\QUINAPRIL
QUETIAPINE vs QUINIDINE