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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4524407 | 5701880 | I | 4524407-7 | 20040510 | 20041103 | 20041117 | PER | 2004UW20644 | ASTRAZENECA PHARMACEUTICALS | 70 | YR | M | N | 205 | LBS | 20041115 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4524407 | 1005480444 | PS | CRESTOR | 1 | ORAL | 10 MG PO | Y | D | 21366 | ||
| 4524407 | 1005525420 | C | SYNTHROID | 1 | |||||||
| 4524407 | 1005525421 | C | ZESTRIL | 1 | |||||||
| 4524407 | 1005525422 | C | INSULIN | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4524407 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 4524407 | BLOOD CREATINE PHOSPHOKINASE INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4524407 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4524407 | 1005480444 | 20031001 | 20040510 |