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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5707649 | 6872524 | I | 5707649-4 | 20080409 | 20080415 | EXP | CHPA2008US06333 | NOVARTIS CONSUMER HEALTH, INC. | 68 | YR | M | N | 20080412 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5707649 | 1009796308 | PS | BENEFIBER (WHEAT DEXTRIN) | 2 | ORAL | 2 TSP, QD, ORAL | N | D | |||
| 5707649 | 1009844812 | SS | ADVIL LIQUI-GELS | 1 | |||||||
| 5707649 | 1009844817 | SS | ANTIHYPERTENSIVES | 2 | |||||||
| 5707649 | 1009844818 | C | PRILOSEC | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5707649 | 1009796308 | NUTRITIONAL SUPPORT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5707649 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5707649 | HAEMATOCHEZIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5707649 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5707649 | 1009796308 | 20060409 |