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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126245661 | 12624566 | 1 | I | 20160412 | 20160729 | 20160805 | 20160805 | PER | US-ASTRAZENECA-2016SE82923 | ASTRAZENECA | 74.00 | YR | F | Y | 0.00000 | 20160805 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126245661 | 12624566 | 1 | PS | PRILOSEC OTC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 1 TABLET, DAILY FOR 14 DAYS OFF AND ON | N | 21229 | MODIFIED-RELEASE TABLET | ||||||||
| 126245661 | 12624566 | 2 | SS | PRILOSEC OTC | OMEPRAZOLE MAGNESIUM | 1 | Oral | N | 21229 | MODIFIED-RELEASE TABLET |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126245661 | 12624566 | Dizziness postural | |
| 126245661 | 12624566 | Dyspnoea | |
| 126245661 | 12624566 | Gastrointestinal disorder | |
| 126245661 | 12624566 | Heart rate irregular |
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 |
|---|---|---|---|---|---|---|
| 126245661 | 12624566 | 1 | 20160530 | 0 |