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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118981942 | 11898194 | 2 | F | 20151219 | 20160829 | 20160108 | 20160909 | EXP | IT-MINISAL02-341119 | IT-TEVA-623011ACC | TEVA | 10.30 | YR | F | Y | 22.00000 | KG | 20160909 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118981942 | 11898194 | 1 | PS | VINCRISTINE | VINCRISTINE | 1 | Intravenous (not otherwise specified) | 1.32 MG WEEKLY | 75493 | 1.32 | MG | ||||||||
| 118981942 | 11898194 | 2 | SS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Intravenous (not otherwise specified) | 40 MILLIGRAM DAILY; 40 MG DAILY | Y | 0 | 40 | MG | |||||||
| 118981942 | 11898194 | 3 | SS | POSACONAZOLE | POSACONAZOLE | 1 | Oral | 160 MILLIGRAM DAILY; 160 MG DAILY | Y | 0 | 160 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118981942 | 11898194 | 1 | Chemotherapy |
| 118981942 | 11898194 | 2 | Leukaemia |
| 118981942 | 11898194 | 3 | Leukaemia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118981942 | 11898194 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118981942 | 11898194 | Hyponatraemia | |
| 118981942 | 11898194 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |