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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4331055 | 4112418 | F | 1 | 4331055-0 | 20040323 | 20040331 | EXP | 2004UW04151 | ASTRAZENECA PHARMACEUTICALS | N | 20040330 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4331055 | 1004758822 | PS | CRESTOR | 1 | ORAL | 10 MG PO | D | D | 21366 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4331055 | OT |
Reactions reported
Event ID | PT |
---|---|
4331055 | NO ADVERSE EFFECT |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4331055 | HP |
Therapies reported
no results found |