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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127834441 | 12783444 | 1 | I | 2016 | 20160725 | 20160927 | 20160927 | PER | US-DRREDDYS-USA/USA/16/0081803 | DR REDDYS | 0.00 | F | Y | 0.00000 | 20160927 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127834441 | 12783444 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | Oral | Y | U | UNKNOWN | 62216 | 250 | MG | CAPSULE | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127834441 | 12783444 | 1 | Sinusitis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127834441 | 12783444 | Abdominal discomfort | |
127834441 | 12783444 | Drug hypersensitivity | |
127834441 | 12783444 | Gastrointestinal pain | |
127834441 | 12783444 | Nausea | |
127834441 | 12783444 | 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 |
---|---|---|---|---|---|---|
127834441 | 12783444 | 1 | 2016 | 0 |