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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125347091 | 12534709 | 1 | I | 20160527 | 20160706 | 20160706 | PER | US-ASTRAZENECA-2016SE58347 | ASTRAZENECA | 0.00 | F | Y | 0.00000 | 20160707 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125347091 | 12534709 | 1 | PS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | U | 19810 | ||||||||||
125347091 | 12534709 | 2 | SS | PRILOSEC OTC | OMEPRAZOLE MAGNESIUM | 1 | Oral | U | 0 | MODIFIED-RELEASE TABLET | |||||||||
125347091 | 12534709 | 3 | C | REGLAN | METOCLOPRAMIDE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125347091 | 12534709 | Depression | |
125347091 | 12534709 | Drug dose omission |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |