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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7233650 | 8140447 | I | 7233650-8 | 20101231 | 20110110 | EXP | 2011SP000401 | SCHERING-PLOUGH CORPORATION | YR | M | N | 20110106 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7233650 | 1015702765 | SS | WARFARIN SODIUM | 1 | ORAL | PO | D | ||||
| 7233650 | 1015702770 | SS | DIGOXIN | 1 | ORAL | PO | D | ||||
| 7233650 | 1015555981 | PS | ZEGERID OTC | 1 | ORAL | ; QD; PO | D | 0DENC | 20130301 | 22281 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7233650 | 1015702765 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7233650 | 1015702770 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7233650 | 1015555981 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7233650 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7233650 | WEIGHT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 7233650 | CSM |
Therapies reported
| no results found |