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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4964432 | 6026857 | I | 4964432-5 | 20060204 | 20060320 | 20060331 | EXP | 2006035773 | PFIZER INC. | 61 | YR | F | N | 290 | LBS | 20060328 | CN | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4964432 | 1007135812 | PS | ROLAIDS EXTRA STRENGTH (MAGNESIUM HYDROXIDE, CALCIUM CARBONATE) | 2 | ORAL | 1 TABLET DAILY, ORAL | U | U | 58525V | 20080630 | |
| 4964432 | 1007177559 | C | VERAPAMIL | 1 | |||||||
| 4964432 | 1007177560 | C | ESTROGEN NOS (ESTROGEN NOS) | 2 | |||||||
| 4964432 | 1007177561 | SS | SPIRONOLACTONE | 1 | |||||||
| 4964432 | 1007177562 | C | KETOROLAC TROMETHAMINE | 1 | |||||||
| 4964432 | 1007177563 | C | RANITIDINE HYDROCHLORIDE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4964432 | 1007135812 | ABDOMINAL DISCOMFORT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4964432 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4964432 | NEPHROLITHIASIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4964432 | CSM |
| 4964432 | FGN |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4964432 | 1007135812 | 20060204 |