Does CLOZAPINE Cause Product dose omission? 206 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 206 reports of Product dose omission have been filed in association with CLOZAPINE (CLOZAPINE). This represents 0.2% of all adverse event reports for CLOZAPINE.
206
Reports of Product dose omission with CLOZAPINE
0.2%
of all CLOZAPINE reports
1
Deaths
169
Hospitalizations
How Dangerous Is Product dose omission From CLOZAPINE?
Of the 206 reports, 1 (0.5%) resulted in death, 169 (82.0%) required hospitalization, and 3 (1.5%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOZAPINE. However, 206 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which CLOZAPINE Alternatives Have Lower Product dose omission 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