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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125267412 | 12526741 | 2 | F | 20160718 | 20160705 | 20160801 | EXP | US-AUROBINDO-AUR-APL-2016-08597 | AUROBINDO | 17.00 | YR | F | Y | 0.00000 | 20160730 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125267412 | 12526741 | 1 | PS | PREDNISONE. | PREDNISONE | 1 | Unknown | 60 MG, UNK | U | 84774 | 60 | MG | |||||||
| 125267412 | 12526741 | 2 | SS | TACROLIMUS. | TACROLIMUS | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125267412 | 12526741 | 1 | Nephrotic syndrome |
| 125267412 | 12526741 | 2 | Nephrotic syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125267412 | 12526741 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125267412 | 12526741 | Back pain | |
| 125267412 | 12526741 | Fatigue | |
| 125267412 | 12526741 | Hyperuricaemia | |
| 125267412 | 12526741 | Nausea | |
| 125267412 | 12526741 | Vomiting | |
| 125267412 | 12526741 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |