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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125980282 | 12598028 | 2 | F | 20160607 | 20160915 | 20160726 | 20160921 | EXP | CA-HLSUS-2016-CA-000218 | HLS THERAPEUTICS | 58.00 | YR | A | M | Y | 86.64000 | KG | 20160921 | OT | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125980282 | 12598028 | 1 | PS | CLOZARIL | CLOZAPINE | 1 | Oral | 350 MG QHS | 0 | 350 | MG | TABLET | QD |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125980282 | 12598028 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125980282 | 12598028 | Dizziness | |
125980282 | 12598028 | Eye contusion | |
125980282 | 12598028 | Head injury | |
125980282 | 12598028 | Loss of consciousness | |
125980282 | 12598028 | Scab | |
125980282 | 12598028 | Skin abrasion |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125980282 | 12598028 | 1 | 19970320 | 0 |