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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127823471 | 12782347 | 1 | I | 20160905 | 20160913 | 20160927 | 20160927 | EXP | GB-AUROBINDO-AUR-APL-2016-11664 | AUROBINDO | 54.00 | YR | F | Y | 71.00000 | KG | 20160927 | MD | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127823471 | 12782347 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | U | U | 65256 | |||||||||
127823471 | 12782347 | 2 | C | NITROFURANTOIN. | NITROFURANTOIN | 1 | Unknown | 1 DF, TWO TIMES A DAY | 10 | DF | U | U | 0 | 1 | DF | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127823471 | 12782347 | 1 | Product used for unknown indication |
127823471 | 12782347 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127823471 | 12782347 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127823471 | 12782347 | Diarrhoea | |
127823471 | 12782347 | Rectal haemorrhage |
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 |
---|---|---|---|---|---|---|
127823471 | 12782347 | 1 | 20160831 | 0 | ||
127823471 | 12782347 | 2 | 20160831 | 0 |