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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127317911 | 12731791 | 1 | I | 20160616 | 0 | 20160909 | 20160909 | DIR | FDA-CTU | 76.00 | YR | F | N | 80.00000 | LBS | 20160729 | Y | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127317911 | 12731791 | 1 | PS | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | Oral | Y | 655171 | 201802 | 0 | 1 | DF | COATED TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127317911 | 12731791 | 1 | Gastrooesophageal reflux disease |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127317911 | 12731791 | HO |
127317911 | 12731791 | RI |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127317911 | 12731791 | Diarrhoea | |
127317911 | 12731791 | Nausea | |
127317911 | 12731791 | Vomiting |
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 |
---|---|---|---|---|---|---|
127317911 | 12731791 | 1 | 20160615 | 20160616 | 0 |