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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7232393 | 8140440 | I | 7232393-4 | 20101101 | 20101221 | 20110105 | EXP | 2010SP065780 | SCHERING-PLOUGH CORPORATION | 60 | YR | F | N | 20101223 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7232393 | 1015550673 | PS | ZEGERID OTC | 1 | ORAL | PO | N | D | 9D10NC | 20111001 | 22281 |
| 7232393 | 1015675067 | C | MULTIVITAMIN | 1 | |||||||
| 7232393 | 1015675076 | C | ASPIRIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7232393 | 1015550673 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7232393 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7232393 | ABDOMINAL PAIN UPPER |
| 7232393 | VOMITING |
| 7232393 | OESOPHAGEAL PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 7232393 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7232393 | 1015550673 | 20101128 |