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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7266811 | 8140448 | I | 7266811-2 | 20110111 | 20110121 | EXP | 2011SP001916 | SCHERING-PLOUGH CORPORATION | YR | N | 20110119 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7266811 | 1015685615 | PS | ZEGERID OTC | 1 | ORAL | PO | D | D | 22281 | ||
| 7266811 | 1015749655 | SS | LISINOPRIL | 1 | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7266811 | 1015685615 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7266811 | 1015749655 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7266811 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7266811 | ANGIOEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 7266811 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7266811 | 1015685615 | 3 | MON |