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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126022551 | 12602255 | 1 | I | 20150826 | 20160728 | 20160728 | PER | US-DRREDDYS-USA/USA/15/0050360 | DR REDDYS | 0.00 | M | Y | 90.71000 | KG | 20160728 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126022551 | 12602255 | 1 | PS | OMEPRAZOLE MAGNESIUM DELAYED RELEASE OTC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 79C408290 | 78878 | 20.6 | MG | CAPSULE | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126022551 | 12602255 | 1 | Dyspepsia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126022551 | 12602255 | Accidental exposure to product | |
126022551 | 12602255 | Extra dose administered | |
126022551 | 12602255 | No adverse event |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |