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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4465960 | 5664776 | I | 4465960-1 | 20030801 | 20040916 | 20040930 | EXP | 2004234133FR | PFIZER INC. | M | N | 20040927 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4465960 | 1005264986 | PS | CELEBREX | 1 | ORAL | 200 MG, QD, ORAL | D | D | 20998 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4465960 | 1005264986 | OSTEOARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
4465960 | DE |
Reactions reported
Event ID | PT |
---|---|
4465960 | OESOPHAGEAL VARICES HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4465960 | FGN |
4465960 | OTH |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4465960 | 1005264986 | 20030801 | 20030801 |