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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126217511 | 12621751 | 1 | I | 20151016 | 20160804 | 20160804 | PER | US-DRREDDYS-USA/USA/15/0053494 | DR REDDYS | 0.00 | F | Y | 0.00000 | 20160804 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126217511 | 12621751 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Oral | N | UNKNOWN | 75593 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126217511 | 12621751 | 1 | Cystitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126217511 | 12621751 | OT |
| 126217511 | 12621751 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126217511 | 12621751 | Anxiety | |
| 126217511 | 12621751 | Depression | |
| 126217511 | 12621751 | Diarrhoea | |
| 126217511 | 12621751 | Dysgeusia | |
| 126217511 | 12621751 | Nausea | |
| 126217511 | 12621751 | Nightmare | |
| 126217511 | 12621751 | Pain | |
| 126217511 | 12621751 | Pyrexia | |
| 126217511 | 12621751 | Skin sensitisation | |
| 126217511 | 12621751 | Suicidal ideation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |