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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127750531 | 12775053 | 1 | I | 20160905 | 20160913 | 20160923 | 20160923 | EXP | GB-MHRA-TPP25222081C1164154YC1473084850330 | GB-TEVA-693730ACC | TEVA | 54.00 | YR | F | Y | 71.00000 | KG | 20160923 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127750531 | 12775053 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | U | U | 61926 | ||||||||||
| 127750531 | 12775053 | 2 | C | NITROFURANTOIN. | NITROFURANTOIN | 1 | 2 DOSAGE FORMS DAILY; | 10 | DF | 0 | 1 | DF | BID |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127750531 | 12775053 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127750531 | 12775053 | Diarrhoea | |
| 127750531 | 12775053 | 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 |
|---|---|---|---|---|---|---|
| 127750531 | 12775053 | 1 | 20160831 | 0 | ||
| 127750531 | 12775053 | 2 | 20160831 | 0 |