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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126632911 | 12663291 | 1 | I | 20160618 | 0 | 20160817 | 20160817 | DIR | 34.00 | YR | F | N | 118.00000 | LBS | 20160816 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126632911 | 12663291 | 1 | PS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | Y | N | 0 | 1 | DF | COATED TABLET | QD | |||||
126632911 | 12663291 | 3 | C | MULTIVITAMIN | VITAMINS | 1 | 0 | ||||||||||||
126632911 | 12663291 | 5 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126632911 | 12663291 | 1 | Sinusitis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126632911 | 12663291 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126632911 | 12663291 | Pain in extremity | |
126632911 | 12663291 | Tendonitis | |
126632911 | 12663291 | Weight bearing difficulty |
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 |
---|---|---|---|---|---|---|
126632911 | 12663291 | 1 | 20160618 | 20160628 | 0 |