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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4432365 | 4184492 | F | 1 | 4432365-9 | 20031127 | 20040805 | 20040818 | EXP | 2004047915 | WWS PFIZER INC | 66 | YR | M | N | 230 | LBS | 20040817 | MD | 20031128 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4432365 | 1005142413 | PS | LIPITOR | 1 | D | D | 20702 | ||||
| 4432365 | 1005160660 | C | ALL OTHER THERAPEUTIC PRODUCTS (ALL OTHER THERAPEUTIC PRODUCTS) | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4432365 | 1005142413 | BLOOD CHOLESTEROL INCREASED |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4432365 | DE |
| 4432365 | HO |
| 4432365 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4432365 | CARDIAC DISORDER |
| 4432365 | CEREBROVASCULAR ACCIDENT |
| 4432365 | DIFFICULTY IN WALKING |
| 4432365 | MYALGIA |
| 4432365 | PAIN IN EXTREMITY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4432365 | CSM |
| 4432365 | HP |
Therapies reported
| no results found |