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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
107972822 | 10797282 | 2 | F | 20160708 | 20150216 | 20160713 | EXP | US-ASTRAZENECA-2015SE11543 | ASTRAZENECA | 71.00 | YR | F | Y | 0.00000 | 20160713 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
107972822 | 10797282 | 1 | PS | ESOMEPRAZOLE MAGNESIUM. | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | U | 0 | ||||||||||
107972822 | 10797282 | 2 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | U | 0 | ||||||||||
107972822 | 10797282 | 3 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | GASEC | U | 0 | |||||||||
107972822 | 10797282 | 4 | SS | GAS-X | DIMETHICONE | 1 | Unknown | U | 0 | ||||||||||
107972822 | 10797282 | 5 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
107972822 | 10797282 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
107972822 | 10797282 | Aplasia | |
107972822 | 10797282 | Drug ineffective | |
107972822 | 10797282 | Dyspepsia | |
107972822 | 10797282 | Gastrooesophageal reflux disease | |
107972822 | 10797282 | Hernia | |
107972822 | 10797282 | Malaise | |
107972822 | 10797282 | Nausea | |
107972822 | 10797282 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |