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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6251651 | 6890924 | F | 6251651-3 | 20090624 | 20090630 | EXP | US-PFIZER INC-2009154829 | PFIZERINC | M | Y | 20090630 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6251651 | 1011816546 | PS | BEXTRA | 1 | 021341 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6251651 | 1011816546 | ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
6251651 | HO |
6251651 | OT |
Reactions reported
Event ID | PT |
---|---|
6251651 | TRANSIENT ISCHAEMIC ATTACK |
6251651 | VISUAL ACUITY REDUCED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |