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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125809382 | 12580938 | 2 | F | 20160323 | 20160825 | 20160721 | 20160830 | EXP | JP-GILEAD-2016-0219089 | GILEAD | 70.00 | YR | E | M | Y | 0.00000 | 20160830 | MD | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125809382 | 12580938 | 1 | PS | SOVALDI | SOFOSBUVIR | 1 | Oral | UNK | 204671 | TABLET | |||||||||
| 125809382 | 12580938 | 2 | SS | COPEGUS | RIBAVIRIN | 1 | Oral | UNK MG, UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125809382 | 12580938 | 1 | Hepatic cirrhosis |
| 125809382 | 12580938 | 2 | Hepatic cirrhosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125809382 | 12580938 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125809382 | 12580938 | Drug ineffective | |
| 125809382 | 12580938 | Hepatitis C | |
| 125809382 | 12580938 | Hepatocellular carcinoma |
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 |
|---|---|---|---|---|---|---|
| 125809382 | 12580938 | 1 | 20151202 | 20160223 | 0 | |
| 125809382 | 12580938 | 2 | 20151202 | 20160223 | 0 |