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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 76405884 | 7640588 | 4 | F | 20091114 | 20160805 | 20101026 | 20160811 | EXP | PHHY2010US68353 | NOVARTIS | 67.39 | YR | F | Y | 0.00000 | 20160811 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 76405884 | 7640588 | 1 | PS | RECLAST | ZOLEDRONIC ACID | 1 | Intravenous drip | UNK | U | U | 21817 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 76405884 | 7640588 | 1 | Osteitis deformans |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 76405884 | 7640588 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 76405884 | 7640588 | Anuria | |
| 76405884 | 7640588 | Influenza like illness | |
| 76405884 | 7640588 | Pain | |
| 76405884 | 7640588 | Tremor | |
| 76405884 | 7640588 | Urinary tract disorder | |
| 76405884 | 7640588 | Urine flow decreased | |
| 76405884 | 7640588 | Urine output 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 |
|---|---|---|---|---|---|---|
| 76405884 | 7640588 | 1 | 20091114 | 0 |