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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5039985 | 6075132 | I | 5039985-1 | 20060621 | 20060630 | EXP | 2006UW13169 | AZPRODUW00 | 77 | YR | F | Y | 59 | KG | 20060630 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5039985 | 1007429048 | PS | CRESTOR | 1 | ORAL | 021366 | |||||
| 5039985 | 1007429049 | SS | CRESTOR | 1 | ORAL | 10 MG 1/2 TABLET | 021366 | ||||
| 5039985 | 1007429050 | C | TOPROL-XL | 1 | |||||||
| 5039985 | 1007429051 | C | LEVOTHYROXINE SODIUM | 1 | |||||||
| 5039985 | 1007429052 | C | ASPIRIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5039985 | 1007429048 | BLOOD CHOLESTEROL INCREASED |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5039985 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5039985 | MACULAR DEGENERATION |
| 5039985 | MUSCLE SPASMS |
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 |
|---|---|---|---|---|---|
| 5039985 | 1007429048 | 20040101 | 6 | MON | |
| 5039985 | 1007429049 | 20060101 |