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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903474 | 6775420 | I | 5903474-X | 20080101 | 20080922 | 20080930 | PER | US-BAYER-200813839BCC | BAYER HEALTHCARE LLC | 65 | YR | M | Y | 78 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903474 | 1010520645 | PS | ALEVE | 1 | ORAL | TOTAL DAILY DOSE: 440 MG UNIT DOSE: 220 MG | UNK | 020204 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5903474 | 1010520645 | ARTHRALGIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5903474 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5903474 | ASTHENIA |
| 5903474 | FAECES DISCOLOURED |
| 5903474 | GASTROINTESTINAL HAEMORRHAGE |
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 |
|---|---|---|---|---|---|
| 5903474 | 1010520645 | 20080101 | 20080101 | 4 | DAY |