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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523397 | 7234935 | I | 6523397-5 | 20091221 | 20091221 | 20091231 | EXP | JP-ROCHE-676810 | ROCHE | 80 | YR | M | Y | 20091231 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523397 | 1012885637 | PS | TAMIFLU | 1 | ORAL | 021087 | |||||
| 6523397 | 1012885638 | C | MAXIPIME | 1 | |||||||
| 6523397 | 1012885639 | C | TS-1 | 2 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523397 | 1012885637 | INFLUENZA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523397 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6523397 | BLOOD CREATINE PHOSPHOKINASE INCREASED |
| 6523397 | RHABDOMYOLYSIS |
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 |
|---|---|---|---|---|---|
| 6523397 | 1012885637 | 20091220 | 20091221 | ||
| 6523397 | 1012885638 | 20091220 | |||
| 6523397 | 1012885639 | 20080101 | 20091201 |