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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8478674 | 8643666 | I | 8478674-8 | 20120628 | 20120629 | EXP | US-ROCHE-1082713 | ROCHE | YR | M | Y | 20120629 | CN | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8478674 | 1020128099 | PS | AVASTIN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8478674 | 1020128099 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
8478674 | DE |
Reactions reported
Event ID | PT |
---|---|
8478674 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |