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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5119579 | 6144840 | I | 5119579-X | 20060921 | 20060929 | EXP | 2006115116 | PFIZER INC | 68 | YR | F | N | 20060928 | OT | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5119579 | 1007725115 | PS | ATORVASTATIN CALCIUM | 1 | ORAL | 20 MG, ORAL | U | D | 20702 | ||
5119579 | 1007746634 | C | BENDROFLUMETHIAZIDE | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5119579 | 1007725115 | HYPERCHOLESTEROLAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
5119579 | OT |
Reactions reported
Event ID | PT |
---|---|
5119579 | AGGRESSION |
5119579 | ANGER |
5119579 | MOOD SWINGS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5119579 | FGN |
5119579 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5119579 | 1007725115 | 20060815 | 20060825 |