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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124741692 | 12474169 | 2 | F | 20160630 | 20160616 | 20160706 | EXP | US-009507513-1606USA006040 | MERCK | 61.00 | YR | M | Y | 0.00000 | 20160706 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124741692 | 12474169 | 1 | PS | ZEPATIER | ELBASVIRGRAZOPREVIR | 1 | Oral | UNK, QD | Y | 208261 | TABLET | QD | |||||||
| 124741692 | 12474169 | 2 | SS | REBETOL | RIBAVIRIN | 1 | Oral | 200 MG, QD | U | 0 | 200 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124741692 | 12474169 | 1 | Chronic hepatitis C |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124741692 | 12474169 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124741692 | 12474169 | Dizziness | |
| 124741692 | 12474169 | Fatigue | |
| 124741692 | 12474169 | Lethargy | |
| 124741692 | 12474169 | Ocular icterus |
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 |
|---|---|---|---|---|---|---|
| 124741692 | 12474169 | 1 | 20160519 | 0 |