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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125863221 | 12586322 | 1 | I | 20160721 | 20160725 | 20160725 | PER | US-ASTRAZENECA-2016SE79215 | ASTRAZENECA | 57.00 | YR | F | Y | 0.00000 | 20160725 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125863221 | 12586322 | 1 | PS | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | UNK | U | 0 | |||||||||
| 125863221 | 12586322 | 2 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | UNK | U | 0 | |||||||||
| 125863221 | 12586322 | 3 | SS | PREVACID | LANSOPRAZOLE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125863221 | 12586322 | Abdominal pain upper | |
| 125863221 | 12586322 | Dystonia | |
| 125863221 | 12586322 | Muscle spasms | |
| 125863221 | 12586322 | Musculoskeletal stiffness | |
| 125863221 | 12586322 | Paraesthesia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |