Does CLOZAPINE Cause Wrong patient received product? 198 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 198 reports of Wrong patient received product have been filed in association with CLOZAPINE (CLOZAPINE). This represents 0.2% of all adverse event reports for CLOZAPINE.
198
Reports of Wrong patient received product with CLOZAPINE
0.2%
of all CLOZAPINE reports
15
Deaths
89
Hospitalizations
How Dangerous Is Wrong patient received product From CLOZAPINE?
Of the 198 reports, 15 (7.6%) resulted in death, 89 (44.9%) required hospitalization, and 37 (18.7%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOZAPINE. However, 198 reports have been filed with the FAERS database.
What Other Side Effects Does CLOZAPINE Cause?
Neutropenia (18,981)
Hospitalisation (12,144)
Death (9,500)
Schizophrenia (3,991)
White blood cell count decreased (3,454)
Off label use (3,192)
Neutrophil count increased (3,125)
Drug ineffective (3,105)
Neutrophilia (3,105)
White blood cell count increased (2,988)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
LAMOTRIGINE (112)
Which CLOZAPINE Alternatives Have Lower Wrong patient received product Risk?
CLOZAPINE vs CLOZARIL
CLOZAPINE vs COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTEIN C\PROTEIN S HUMAN\PROTHROMBIN
CLOZAPINE vs COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTHROMBIN
CLOZAPINE vs COAGULATION FACTOR IX RECOMBINANT HUMAN
CLOZAPINE vs COAGULATION FACTOR IX RECOMBINANT HUMAN\ISOPROPYL ALCOHOL