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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016621 | 8317511 | I | 8016621-3 | 20070101 | 20111227 | 20111231 | EXP | CHPA2011US018679 | NOVARTIS CONSUMER HEALTH, INC. | 84 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016621 | 1018419895 | PS | KERI ORIGINAL | 2 | TOPICAL | UNK, UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016621 | 1018419895 | THERAPEUTIC SKIN CARE TOPICAL |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016621 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 8016621 | BONE NEOPLASM MALIGNANT |
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 |
|---|---|---|---|---|---|
| 8016621 | 1018419895 | 19720101 | 20070101 |