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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282275 | 6276593 | I | 5282275-2 | 20070309 | 20070320 | 20070331 | EXP | IT-PFIZER INC-2007023147 | PFIZER INC | 35 | YR | F | Y | 20070330 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282275 | 1008316795 | PS | UNASYN | 1 | INTRAVENOUS | TEXT:1G+500 MG; 1 UNIT-FREQ:FREQUENCY: ONCE | 050608 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5282275 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 5282275 | FLUSHING |
| 5282275 | HYPERHIDROSIS |
| 5282275 | HYPERSENSITIVITY |
| 5282275 | HYPOTENSION |
| 5282275 | PARAESTHESIA ORAL |
| 5282275 | PSYCHOMOTOR HYPERACTIVITY |
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 |
|---|---|---|---|---|---|
| 5282275 | 1008316795 | 20070309 | 20070309 |