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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125757481 | 12575748 | 1 | I | 20160608 | 20160720 | 20160720 | PER | US-ASTRAZENECA-2016SE62042 | ASTRAZENECA | 0.00 | M | Y | 77.10000 | KG | 20160720 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125757481 | 12575748 | 1 | PS | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | N | 21153 | ||||||||||
| 125757481 | 12575748 | 2 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | N | 0 | ||||||||||
| 125757481 | 12575748 | 3 | SS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | 0 | 40 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125757481 | 12575748 | 3 | Gastrooesophageal reflux disease |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125757481 | 12575748 | Abdominal discomfort | |
| 125757481 | 12575748 | Drug ineffective | |
| 125757481 | 12575748 | Gastrooesophageal reflux disease |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |