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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016613 | 8317504 | I | 8016613-4 | 20111222 | 20111223 | 20111231 | EXP | CHPA2011US018586 | NOVARTIS CONSUMER HEALTH, INC. | YR | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016613 | 1018419878 | PS | EX-LAX UNKNOWN | 2 | ORAL | UNK, UNK |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016613 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8016613 | RECTAL HAEMORRHAGE |
| 8016613 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 8016613 | 1018419878 | 20111222 | 20111222 | 1 | DAY |