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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4462916 | 4218897 | I | 4462916-X | 20040921 | 20040930 | EXP | US-JNJFOC-20040907317 | JOHNSON + JOHNSON PHARMACEUTICAL | M | Y | 20040930 | MD |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4462916 | 1005251310 | PS | DURAGESIC | 1 | TRANSDERMAL |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4462916 | DE |
Reactions reported
Event ID | PT |
---|---|
4462916 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |