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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6137761 | 6956398 | I | 6137761-X | 20090101 | 20090325 | 20090331 | EXP | JP-ASTRAZENECA-2009AP02207 | AZPRODUW00 | 60 | YR | F | Y | 20090331 | OT | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6137761 | 1011355040 | PS | CRESTOR | 1 | ORAL | 021366 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6137761 | 1011355040 | HYPERCHOLESTEROLAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
6137761 | HO |
Reactions reported
Event ID | PT |
---|---|
6137761 | ALVEOLITIS ALLERGIC |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |