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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810903 | 7449533 | F | 6810903-6 | 20081103 | 20100630 | PER | US-PFIZER INC-2008071970 | PFIZERINC | YR | F | Y | 20100630 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810903 | 1014009999 | PS | ESTRING | 1 | KA993A | 020472 | |||||
| 6810903 | 1014010000 | C | PANTOPRAZOLE | 1 | |||||||
| 6810903 | 1014010001 | C | ALPRAZOLAM | 2 | |||||||
| 6810903 | 1014010002 | C | ETODOLAC | 1 | |||||||
| 6810903 | 1014010003 | C | ATENOLOL | 1 | |||||||
| 6810903 | 1014010004 | C | ALL OTHER THERAPEUTIC PRODUCTS | 2 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6810903 | LABORATORY TEST ABNORMAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6810903 | 1014010004 | 20080201 |