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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4524408 | 5654552 | F | 1 | 4524408-9 | 20041002 | 20041105 | 20041117 | PER | 2004UW20937 | ASTRAZENECA PHARMACEUTICALS | 53 | YR | F | N | 90.718 | KG | 20041110 | OT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4524408 | 1005480446 | PS | CRESTOR | 1 | ORAL | 10 MG QD PO | Y | D | 21366 | ||
4524408 | 1005527264 | C | MICARDIA/HYDROCHLOROTHIAZIDE | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4524408 | 1005480446 | HYPERCHOLESTEROLAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
4524408 | HO |
Reactions reported
Event ID | PT |
---|---|
4524408 | RHABDOMYOLYSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4524408 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4524408 | 1005480446 | 20031203 | 20041002 |