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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6767313 | 7418171 | I | 6767313-X | 20100601 | 20100602 | 20100614 | EXP | US-BAYER-201016591BCC | BAYER HEALTHCARE LLC | 69 | YR | M | Y | 98 | KG | 20100614 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6767313 | 1013856277 | PS | ALEVE (CAPLET) | 1 | ORAL | TOTAL DAILY DOSE: 440 MG UNIT DOSE: 220 MG | UNK | 020204 | |||
| 6767313 | 1013856278 | C | UNKNOWN VITAMINS | 2 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6767313 | 1013856277 | HEADACHE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6767313 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6767313 | AMNESIA |
| 6767313 | SOMNOLENCE |
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 |
|---|---|---|---|---|---|
| 6767313 | 1013856277 | 20100601 |