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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125747001 | 12574700 | 1 | I | 201510 | 20160708 | 20160720 | 20160720 | EXP | CA-PFIZER INC-2016346207 | PFIZER | 41.00 | YR | M | Y | 0.00000 | 20160720 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125747001 | 12574700 | 1 | PS | Tecta | PANTOPRAZOLE MAGNESIUM | 1 | Unknown | UNK | 20987 | PROLONGED-RELEASE TABLET | |||||||||
| 125747001 | 12574700 | 2 | SS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | UNK | 20987 | PROLONGED-RELEASE TABLET | |||||||||
| 125747001 | 12574700 | 3 | C | PREDNISONE. | PREDNISONE | 1 | 10 MG, UNK | 0 | 10 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125747001 | 12574700 | 1 | Gastrooesophageal reflux disease |
| 125747001 | 12574700 | 2 | Gastrooesophageal reflux disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125747001 | 12574700 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125747001 | 12574700 | Condition aggravated | |
| 125747001 | 12574700 | Crohn's disease |
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 |
|---|---|---|---|---|---|---|
| 125747001 | 12574700 | 3 | 20151001 | 0 |