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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125174272 | 12517427 | 2 | F | 200811 | 20160623 | 20160630 | 20160707 | EXP | US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-119265 | RANBAXY | 12.00 | YR | M | Y | 0.00000 | 20160707 | OT | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125174272 | 12517427 | 1 | PS | Triamcinolone | TRIAMCINOLONE | 1 | Subcutaneous | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125174272 | 12517427 | 1 | Keloid scar |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125174272 | 12517427 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125174272 | 12517427 | Dizziness | |
| 125174272 | 12517427 | Eyelid ptosis | |
| 125174272 | 12517427 | Hyperhidrosis | |
| 125174272 | 12517427 | Hypoaesthesia | |
| 125174272 | 12517427 | Retinal artery occlusion |
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 |
|---|---|---|---|---|---|---|
| 125174272 | 12517427 | 1 | 200811 | 0 |