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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125478652 | 12547865 | 2 | F | 20160722 | 20160712 | 20160804 | EXP | GB-AUROBINDO-AUR-APL-2016-07546 | AUROBINDO | 70.00 | YR | F | Y | 0.00000 | 20160804 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125478652 | 12547865 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | 750 MG, TWO TIMES A DAY | Y | U | 77859 | 750 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125478652 | 12547865 | 1 | Infection prophylaxis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125478652 | 12547865 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125478652 | 12547865 | Arthralgia | |
| 125478652 | 12547865 | Groin pain | |
| 125478652 | 12547865 | Normochromic normocytic anaemia | |
| 125478652 | 12547865 | Oedema | |
| 125478652 | 12547865 | Tendon disorder | |
| 125478652 | 12547865 | Tendon rupture | |
| 125478652 | 12547865 | Weight bearing difficulty |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |