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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126251701 | 12625170 | 1 | I | 20160727 | 0 | 20160804 | 20160804 | DIR | 60.00 | YR | M | N | 0.00000 | 20160803 | N | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126251701 | 12625170 | 1 | PS | HARVONI | LEDIPASVIRSOFOSBUVIR | 1 | Oral | 90-400MG QD ORAL | Y | 0 | QD | ||||||||
| 126251701 | 12625170 | 2 | SS | RIBASPHERE | RIBAVIRIN | 1 | Oral | Y | 0 | 600 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126251701 | 12625170 | 1 | Chronic hepatitis C |
| 126251701 | 12625170 | 2 | Chronic hepatitis C |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126251701 | 12625170 | Fatigue | |
| 126251701 | 12625170 | Haemoglobin decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 126251701 | 12625170 | HP |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126251701 | 12625170 | 1 | 20160623 | 0 | ||
| 126251701 | 12625170 | 2 | 20160623 | 0 |