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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126081652 | 12608165 | 2 | F | 201607 | 20160720 | 20160729 | 20160904 | PER | US-ASTRAZENECA-2016SE79758 | ASTRAZENECA | 58.00 | YR | F | Y | 0.00000 | 20160904 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126081652 | 12608165 | 1 | PS | PRILOSEC OTC | OMEPRAZOLE MAGNESIUM | 1 | Oral | Y | 21229 | 1 | DF | MODIFIED-RELEASE TABLET | QD |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126081652 | 12608165 | Back pain | |
| 126081652 | 12608165 | Chest pain | |
| 126081652 | 12608165 | Dyspnoea | |
| 126081652 | 12608165 | Local swelling | |
| 126081652 | 12608165 | Neck pain | |
| 126081652 | 12608165 | Skin burning sensation |
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 |
|---|---|---|---|---|---|---|
| 126081652 | 12608165 | 1 | 20160703 | 20160717 | 0 |