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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 96820351 | 9682035 | 1 | I | 20131106 | 20131111 | 20131111 | EXP | US-GILEAD-2013-0087179 | GILEAD | 65.00 | YR | M | Y | 0.00000 | 20131111 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 96820351 | 9682035 | 1 | PS | RANEXA | 1 | 1000 MG, UNK | D | 21526 | 1000 | MG | TABLET | ||||||||
| 96820351 | 9682035 | 2 | SS | RANEXA | 1 | 500 MG, UNK | D | 21526 | 500 | MG | TABLET | ||||||||
| 96820351 | 9682035 | 3 | SS | RANEXA | 1 | 500 MG, UNK | D | 21526 | 500 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 96820351 | 9682035 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 96820351 | 9682035 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 96820351 | 9682035 | Angina pectoris |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |