Does QUETIAPINE Cause Product administration error? 174 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 174 reports of Product administration error have been filed in association with QUETIAPINE (Quetiapine). This represents 0.2% of all adverse event reports for QUETIAPINE.
174
Reports of Product administration error with QUETIAPINE
0.2%
of all QUETIAPINE reports
4
Deaths
117
Hospitalizations
How Dangerous Is Product administration error From QUETIAPINE?
Of the 174 reports, 4 (2.3%) resulted in death, 117 (67.2%) required hospitalization, and 13 (7.5%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for QUETIAPINE. However, 174 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which QUETIAPINE Alternatives Have Lower Product administration error Risk?
QUETIAPINE vs QUILLIVANT
QUETIAPINE vs QUINACRINE
QUETIAPINE vs QUINAPRIL
QUETIAPINE vs QUINAPRIL\QUINAPRIL
QUETIAPINE vs QUINIDINE