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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7243267 | 8140440 | F | 1 | 7243267-7 | 20101126 | 20110105 | 20110118 | EXP | 2010SP065780 | SCHERING-PLOUGH CORPORATION | 59 | YR | F | N | 114 | LBS | 20110114 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7243267 | 1015591647 | PS | ZEGERID OTC | 1 | ORAL | 20 MG;QD;PO | N | D | 9D10NC | 20111001 | 22281 |
| 7243267 | 1015709417 | C | VITAMIN TAB | 1 | |||||||
| 7243267 | 1015709432 | C | ASPIRIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7243267 | 1015591647 | DYSPEPSIA |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7243267 | ABDOMINAL PAIN UPPER |
| 7243267 | DISCOMFORT |
| 7243267 | OESOPHAGEAL PAIN |
| 7243267 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 7243267 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7243267 | 1015591647 | 20101119 | 20101127 |