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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4369782 | 4145529 | F | 1 | 4369782-1 | 20040401 | 20040513 | 20040525 | EXP | 2004030847 | PFIZER INC WWS | 77 | YR | F | N | 20040524 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4369782 | 1004911429 | PS | ZITHROMAX | 1 | ORAL | 500 MG (, 1 D), ORAL | D | D | 50784 | ||
| 4369782 | 1004928856 | C | PRAVASTATIN SODIUM | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4369782 | 1004911429 | UPPER RESPIRATORY TRACT INFLAMMATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4369782 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4369782 | ARTERIOSCLEROSIS |
| 4369782 | COLITIS ISCHAEMIC |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4369782 | CR |
| 4369782 | FGN |
| 4369782 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4369782 | 1004911429 | 20040427 | 20040429 |