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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126278931 | 12627893 | 1 | I | 20150425 | 20160726 | 20160807 | 20160807 | EXP | DE-DEXPHARM-20161664 | DEXCEL | YU, M.; QIAN, J.; GUO, D.; LI, L.; LIU, X. SEVERE ADVERSE REACTIONS CAUSED BY OMEPRAZOLE: A CASE REPORT. EXPERIMENTAL AND THERAPEUTIC MEDICINE 2016, V12, P1103-1106 | 61.00 | YR | A | F | Y | 0.00000 | 20160807 | OT | CN | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126278931 | 12627893 | 1 | PS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | U | U | 0 | 20 | MG | TABLET | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126278931 | 12627893 | 1 | Abdominal discomfort |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126278931 | 12627893 | HO |
| 126278931 | 12627893 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126278931 | 12627893 | Acute kidney injury | |
| 126278931 | 12627893 | Anaphylactic shock | |
| 126278931 | 12627893 | Diarrhoea | |
| 126278931 | 12627893 | Electrolyte imbalance | |
| 126278931 | 12627893 | Metabolic acidosis | |
| 126278931 | 12627893 | Nausea | |
| 126278931 | 12627893 | Rash | |
| 126278931 | 12627893 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |