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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127203341 | 12720334 | 1 | I | 20160728 | 20160825 | 20160907 | 20160907 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123101 | RANBAXY | 80.00 | YR | M | Y | 64.00000 | KG | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127203341 | 12720334 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Oral | 500 MG, BID | 1000 | MG | Y | U | 75747 | 500 | MG | Q12H | |||
127203341 | 12720334 | 2 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | 10 MG, UNK | U | U | 0 | 10 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127203341 | 12720334 | 1 | Urinary tract infection |
127203341 | 12720334 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127203341 | 12720334 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127203341 | 12720334 | Myositis | |
127203341 | 12720334 | Pain | |
127203341 | 12720334 | Rash | |
127203341 | 12720334 | Tendonitis | |
127203341 | 12720334 | White blood cell count increased |
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 |
---|---|---|---|---|---|---|
127203341 | 12720334 | 1 | 20160728 | 20160816 | 0 |