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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523396 | 7234934 | I | 6523396-3 | 20090908 | 20091225 | 20091231 | EXP | JP-ROCHE-676640 | ROCHE | 74 | YR | M | Y | 20091231 | MD | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523396 | 1012885636 | PS | TAMIFLU | 1 | ORAL | 021087 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523396 | 1012885636 | H1N1 INFLUENZA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523396 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6523396 | HEPATITIS FULMINANT |
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 |
|---|---|---|---|---|---|
| 6523396 | 1012885636 | 20090907 | 20090907 |