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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5578156 | 6385955 | F | 5578156-7 | 19970101 | 20071219 | 20071231 | EXP | US-PFIZER INC-2006088309 | PFIZER INC | M | Y | 20071231 | LW | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5578156 | 1009350757 | PS | ATORVASTATIN | 2 | 20702 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5578156 | 1009350757 | BLOOD CHOLESTEROL INCREASED |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5578156 | DS |
| 5578156 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5578156 | AMNESIA |
| 5578156 | BURNING SENSATION |
| 5578156 | CONFUSIONAL STATE |
| 5578156 | DEPRESSION |
| 5578156 | FATIGUE |
| 5578156 | GAIT DISTURBANCE |
| 5578156 | IRRITABILITY |
| 5578156 | MYALGIA |
| 5578156 | MYOPATHY |
| 5578156 | NEUROPATHY PERIPHERAL |
| 5578156 | SENSORY DISTURBANCE |
| 5578156 | SINUSITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |