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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903473 | 6775419 | I | 5903473-8 | 20080918 | 20080918 | 20080930 | EXP | US-BAYER-200813832BCC | BAYER HEALTHCARE LLC | 63 | YR | F | Y | 58 | KG | 20080930 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903473 | 1010520644 | PS | ALEVE | 1 | ORAL | TOTAL DAILY DOSE: 880 MG UNIT DOSE: 220 MG | 219355P | 020204 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5903473 | 1010520644 | ARTHRALGIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5903473 | HO |
| 5903473 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5903473 | ABDOMINAL RIGIDITY |
| 5903473 | DYSURIA |
| 5903473 | NEPHROLITHIASIS |
| 5903473 | RENAL PAIN |
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 |
|---|---|---|---|---|---|
| 5903473 | 1010520644 | 20080911 | 20080918 | 8 | DAY |