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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126015331 | 12601533 | 1 | I | 20131101 | 0 | 20160727 | 20160727 | DIR | 50.00 | YR | F | N | 0.00000 | 20160726 | N | COUNTRY NOT SPECIFIED |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126015331 | 12601533 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | N | Y | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126015331 | 12601533 | 1 | Urinary tract infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126015331 | 12601533 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126015331 | 12601533 | Arthropathy | |
| 126015331 | 12601533 | Asthenia | |
| 126015331 | 12601533 | Blood urine | |
| 126015331 | 12601533 | Gait disturbance | |
| 126015331 | 12601533 | Muscle rupture | |
| 126015331 | 12601533 | Pain in extremity | |
| 126015331 | 12601533 | Plantar fasciitis | |
| 126015331 | 12601533 | Tendon rupture | |
| 126015331 | 12601533 | Tendonitis |
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 |
|---|---|---|---|---|---|---|
| 126015331 | 12601533 | 1 | 20131101 | 20150615 | 0 |