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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125983381 | 12598338 | 1 | I | 20160725 | 0 | 20160726 | 20160726 | DIR | 54.00 | YR | F | N | 0.00000 | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125983381 | 12598338 | 1 | PS | RIBASPHERE | RIBAVIRIN | 1 | Oral | 200MG 2AM AND 2PM ORAL | D | D | 0 | 200 | MG | BID | |||||
125983381 | 12598338 | 2 | SS | SOVALDI | SOFOSBUVIR | 1 | Oral | D | D | 0 | 400 | DF | QD |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125983381 | 12598338 | Gastrooesophageal reflux disease | |
125983381 | 12598338 | Headache | |
125983381 | 12598338 | Pruritus |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | CASEID | RPSR COD |
---|---|---|
125983381 | 12598338 | HP |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125983381 | 12598338 | 1 | 20160620 | 0 | ||
125983381 | 12598338 | 2 | 20160620 | 0 |