Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126600301 | 12660030 | 1 | I | 20160519 | 20160817 | 20160817 | EXP | US-PFIZER INC-2016270889 | PFIZER | SAFFERMAN, A.. UNRELATED AGRANULOCYTOSIS IN A PATIENT TAKING CLOZAPINE. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY. 1993;13(3):218-219 | 45.00 | YR | F | Y | 0.00000 | 20160817 | MD | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126600301 | 12660030 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | 600 MG, EVERY 4 HRS (AS NEEDED) | 18989 | 600 | MG | |||||||||
126600301 | 12660030 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | 18989 | ||||||||||||
126600301 | 12660030 | 3 | SS | IBUPROFEN. | IBUPROFEN | 1 | 18989 | ||||||||||||
126600301 | 12660030 | 4 | SS | CLOZAPINE. | CLOZAPINE | 1 | 350 MG, DAILY (100 MG IN THE MORNING AND 250 MG AT BEDTIME) | 0 | 350 | MG | |||||||||
126600301 | 12660030 | 5 | SS | CLOZAPINE. | CLOZAPINE | 1 | 200 MG, DAILY | 0 | 200 | MG | |||||||||
126600301 | 12660030 | 6 | SS | CLOZAPINE. | CLOZAPINE | 1 | 600 MG, DAILY (SLOWELY TITRATED) | 0 | 600 | MG | |||||||||
126600301 | 12660030 | 7 | SS | CLONAZEPAM. | CLONAZEPAM | 1 | 1 MG, 3X/DAY | 0 | 1 | MG | TID | ||||||||
126600301 | 12660030 | 8 | C | LITHIUM CARBONATE. | LITHIUM CARBONATE | 1 | 900 MG, EVERY NIGHT AT BEDTIME | 0 | 900 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126600301 | 12660030 | 1 | Schizoaffective disorder |
126600301 | 12660030 | 2 | Pain |
126600301 | 12660030 | 3 | Movement disorder |
126600301 | 12660030 | 4 | Tardive dyskinesia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126600301 | 12660030 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126600301 | 12660030 | Agranulocytosis | |
126600301 | 12660030 | Toxicity to various agents |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |