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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125776471 | 12577647 | 1 | I | 201606 | 20160713 | 20160720 | 20160720 | EXP | US-ASTRAZENECA-2016SE76992 | ASTRAZENECA | 966.00 | MON | M | Y | 93.00000 | KG | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125776471 | 12577647 | 1 | PS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 19810 | |||||||||||
| 125776471 | 12577647 | 2 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 19810 | |||||||||||
| 125776471 | 12577647 | 3 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 20.0MG UNKNOWN | 19810 | 20 | MG | ||||||||
| 125776471 | 12577647 | 4 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 20.0MG UNKNOWN | 19810 | 20 | MG | ||||||||
| 125776471 | 12577647 | 5 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 10.0MG UNKNOWN | 19810 | 10 | MG | ||||||||
| 125776471 | 12577647 | 6 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 10.0MG UNKNOWN | 19810 | 10 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125776471 | 12577647 | 1 | Gastrooesophageal reflux disease |
| 125776471 | 12577647 | 2 | Gastrooesophageal reflux disease |
| 125776471 | 12577647 | 3 | Gastrooesophageal reflux disease |
| 125776471 | 12577647 | 4 | Gastrooesophageal reflux disease |
| 125776471 | 12577647 | 5 | Gastrooesophageal reflux disease |
| 125776471 | 12577647 | 6 | Gastrooesophageal reflux disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125776471 | 12577647 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125776471 | 12577647 | Body height decreased | |
| 125776471 | 12577647 | Colon neoplasm | |
| 125776471 | 12577647 | Dizziness | |
| 125776471 | 12577647 | Intentional product misuse | |
| 125776471 | 12577647 | Oesophageal disorder | |
| 125776471 | 12577647 | Off label use |
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 |
|---|---|---|---|---|---|---|
| 125776471 | 12577647 | 5 | 201606 | 0 | ||
| 125776471 | 12577647 | 6 | 201606 | 0 |