Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4430570 | 4122965 | F | 1 | 4430570-9 | 20040322 | 20040816 | 20040818 | EXP | 2004-03-1589 | SCHERING-PLOUGH CORPORATION | 45 | YR | M | N | 67 | KG | 20040816 | MD |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4430570 | 1005132462 | PS | REBETOL | 1 | ORAL | 800 MG ORAL | Y | D | 20903 | ||
4430570 | 1005146993 | SS | INTRON A | 1 | INTRAMUSCULAR | 6 MU INTRAMUSCULAR | Y | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4430570 | 1005132462 | HEPATITIS C |
4430570 | 1005146993 | HEPATITIS C |
Outcome of event
Event ID | OUTC COD |
---|---|
4430570 | HO |
Reactions reported
Event ID | PT |
---|---|
4430570 | GASTROINTESTINAL HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4430570 | FGN |
4430570 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4430570 | 1005132462 | 20040224 | 20040301 | ||
4430570 | 1005146993 | 20040224 | 20040301 |