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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127833411 | 12783341 | 1 | I | 20160902 | 20160913 | 20160927 | 20160927 | EXP | GB-AUROBINDO-AUR-APL-2016-11659 | AUROBINDO | 37.00 | YR | M | Y | 73.00000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127833411 | 12783341 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | U | U | 65256 | |||||||||
| 127833411 | 12783341 | 2 | C | TRIMETHOPRIM. | TRIMETHOPRIM | 1 | Unknown | 1 DF, TWO TIMES A DAY | 2 | DF | U | 0 | 1 | DF | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127833411 | 12783341 | 1 | Product used for unknown indication |
| 127833411 | 12783341 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127833411 | 12783341 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127833411 | 12783341 | Peripheral swelling | |
| 127833411 | 12783341 | Pruritus | |
| 127833411 | 12783341 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 127833411 | 12783341 | 1 | 20160901 | 0 | ||
| 127833411 | 12783341 | 2 | 20160901 | 0 |