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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327665 | 6314676 | F | 5327665-4 | 20070425 | 20070514 | 20070517 | EXP | B0471072A | GLAXOSMITHKLINE | 59 | YR | M | Y | 20070517 | CN | ITALY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327665 | 1008489329 | PS | AUGMENTIN '125' | 1 | INTRAVENOUS | 3G PER DAY | 50564 | ||||
| 5327665 | 1008489330 | SS | PHENYTOIN | 1 | ORAL | 300MG PER DAY | |||||
| 5327665 | 1008489331 | C | PARACETAMOL | 2 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5327665 | 1008489329 | PYREXIA |
| 5327665 | 1008489330 | GLIOMA |
| 5327665 | 1008489331 | PYREXIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5327665 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5327665 | EOSINOPHILIA |
| 5327665 | GENERALISED ERYTHEMA |
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 |
|---|---|---|---|---|---|
| 5327665 | 1008489329 | 20070422 | 20070425 | 4 | DAY |
| 5327665 | 1008489330 | 20070406 | 20070502 | 27 | DAY |