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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5797493 | 6695188 | I | 5797493-4 | 20080610 | 20080620 | 20080630 | EXP | 2008016536 | JOHNSON AND JOHNSON GROUP OF CONSUMER COMPANIES | 79 | YR | F | N | 128 | LBS | 20080627 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5797493 | 1010120669 | PS | LISTERINE WHITENING PRE-BRUSH RINSE (NO ACTIVE INGREDIENT) | 2 | ORAL | 3 TEASPOONS TWICE DAILY (2 IN 1 D), ORAL | N | D | |||
5797493 | 1010152090 | C | DARVON | 1 | |||||||
5797493 | 1010152091 | C | ATENOLOL | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5797493 | OT |
Reactions reported
Event ID | PT |
---|---|
5797493 | ORAL PAIN |
5797493 | THERMAL BURN |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5797493 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5797493 | 1010120669 | 20080609 | 20080611 |