Does CLOZAPINE Cause Product administration interrupted? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Product administration interrupted have been filed in association with CLOZAPINE (CLOZAPINE). This represents 0.0% of all adverse event reports for CLOZAPINE.
26
Reports of Product administration interrupted with CLOZAPINE
0.0%
of all CLOZAPINE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Product administration interrupted From CLOZAPINE?
Of the 26 reports, 13 (50.0%) required hospitalization, and 1 (3.8%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOZAPINE. However, 26 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 administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which CLOZAPINE Alternatives Have Lower Product administration interrupted 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