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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117960443 | 11796044 | 3 | F | 20151113 | 20160817 | 20151203 | 20160818 | EXP | IT-ROCHE-1663129 | ROCHE | 69.22 | YR | M | Y | 0.00000 | 20160818 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117960443 | 11796044 | 1 | PS | COPEGUS | RIBAVIRIN | 1 | Oral | 42 TABLETS | Y | 21511 | FILM-COATED TABLET | ||||||||
| 117960443 | 11796044 | 2 | SS | HARVONI | LEDIPASVIRSOFOSBUVIR | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117960443 | 11796044 | 1 | Liver transplant |
| 117960443 | 11796044 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117960443 | 11796044 | OT |
| 117960443 | 11796044 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117960443 | 11796044 | Anaemia | |
| 117960443 | 11796044 | Condition aggravated |
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 |
|---|---|---|---|---|---|---|
| 117960443 | 11796044 | 1 | 20151113 | 0 |