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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016612 | 8317503 | I | 8016612-2 | 20111221 | 20111222 | 20111231 | EXP | CHPA2011US018566 | NOVARTIS CONSUMER HEALTH, INC. | 82 | YR | F | Y | 20111231 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016612 | 1018419876 | SS | BENEFIBER ORANGE POWDER | 2 | ORAL | 1 TSP, UNK | |||||
| 8016612 | 1018419875 | PS | BENEFIBER W/ WHEAT DEXTRIN | 2 | ORAL | 1 TSP, A DAY | 10116296 | ||||
| 8016612 | 1018419877 | SS | BENEFIBER W/ WHEAT DEXTRIN | 2 | ORAL | UNK, UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016612 | 1018419875 | NUTRITIONAL SUPPORT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016612 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8016612 | NEURODEGENERATIVE DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |