Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125733581 | 12573358 | 1 | I | 20160706 | 20160720 | 20160720 | EXP | CA-JNJFOC-20160710627 | JOHNSON AND JOHNSON | 65.00 | YR | A | M | Y | 0.00000 | 20160720 | PH | CA | CA |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125733581 | 12573358 | 1 | PS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | U | U | 19872 | UNKNOWN | ||||||||
| 125733581 | 12573358 | 2 | SS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | U | U | 19872 | 1 | G | UNKNOWN | ||||||
| 125733581 | 12573358 | 3 | I | APO-WARFARIN | WARFARIN SODIUM | 1 | Oral | U | 0 | 5 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125733581 | 12573358 | 2 | Product used for unknown indication |
| 125733581 | 12573358 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125733581 | 12573358 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125733581 | 12573358 | Atrial fibrillation | |
| 125733581 | 12573358 | Drug interaction | |
| 125733581 | 12573358 | International normalised ratio increased | |
| 125733581 | 12573358 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |