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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126245781 | 12624578 | 1 | I | 20160722 | 20160805 | 20160805 | EXP | FR-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-120918 | RANBAXY | 58.00 | YR | F | Y | 0.00000 | 20160805 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126245781 | 12624578 | 1 | PS | Esomeprazole | ESOMEPRAZOLE | 1 | Unknown | 20 MG, DAILY | U | 200882 | 20 | MG | |||||||
| 126245781 | 12624578 | 2 | I | VALPROIC ACID. | VALPROIC ACID | 1 | Unknown | 1500 MG, DAILY | U | 0 | 1500 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126245781 | 12624578 | 1 | Product used for unknown indication |
| 126245781 | 12624578 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126245781 | 12624578 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126245781 | 12624578 | Drug interaction | |
| 126245781 | 12624578 | Hepatic function abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |