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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126579534 | 12657953 | 4 | F | 20160816 | 20160915 | 20160816 | 20160916 | EXP | CA-HLSUS-2016-CA-000366 | HLS THERAPEUTICS | 71.60 | YR | E | F | Y | 0.00000 | 20160916 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126579534 | 12657953 | 1 | PS | CLOZARIL | CLOZAPINE | 1 | Oral | D | 0 | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126579534 | 12657953 | DE |
| 126579534 | 12657953 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126579534 | 12657953 | Anaemia | |
| 126579534 | 12657953 | Death | |
| 126579534 | 12657953 | Eating disorder | |
| 126579534 | 12657953 | Haematocrit decreased | |
| 126579534 | 12657953 | Malnutrition | |
| 126579534 | 12657953 | Off label use | |
| 126579534 | 12657953 | Red blood cell count decreased | |
| 126579534 | 12657953 | Weight decreased | |
| 126579534 | 12657953 | White blood cell count decreased |
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 |
|---|---|---|---|---|---|---|
| 126579534 | 12657953 | 1 | 20140912 | 20160915 | 0 |