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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127649902 | 12764990 | 2 | F | 20140602 | 20161004 | 20160921 | 20160921 | EXP | GB-DEXPHARM-20161954 | DEXCEL | 30.00 | YR | A | M | Y | 114.30000 | KG | 20161009 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127649902 | 12764990 | 1 | PS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | DAILY DOSE: 20 MG MILLGRAM(S) EVERY DAYS | 20720 | MG | Y | U | 0 | 20 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127649902 | 12764990 | 1 | Irritable bowel syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127649902 | 12764990 | DS |
| 127649902 | 12764990 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127649902 | 12764990 | Asthenia | |
| 127649902 | 12764990 | Chest pain | |
| 127649902 | 12764990 | Dizziness | |
| 127649902 | 12764990 | Fatigue | |
| 127649902 | 12764990 | Nausea |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127649902 | 12764990 | 1 | 20110802 | 20160407 | 0 |