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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4331056 | 4121328 | I | 4331056-2 | 20040325 | 20040331 | EXP | 2004UW05924 | ASTRAZENECA PHARMACEUTICALS | F | N | 20040330 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4331056 | 1004758823 | PS | CRESTOR | 1 | ORAL | 10 MG PO | D | D | 21366 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4331056 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 4331056 | DIZZINESS |
| 4331056 | DYSKINESIA |
| 4331056 | TRANSIENT ISCHAEMIC ATTACK |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4331056 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4331056 | 1004758823 | 20040101 |