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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127135711 | 12713571 | 1 | I | 20160822 | 20160903 | 20160903 | EXP | AU-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-123242 | RANBAXY | 21.00 | YR | M | Y | 0.00000 | 20160903 | OT | GB | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127135711 | 12713571 | 1 | PS | Zoledronic Acid | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 4 UNK, UNK | U | 202746 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127135711 | 12713571 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127135711 | 12713571 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127135711 | 12713571 | Acute phase reaction | |
| 127135711 | 12713571 | Arthralgia | |
| 127135711 | 12713571 | Myalgia | |
| 127135711 | 12713571 | Nausea | |
| 127135711 | 12713571 | Pyrexia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |