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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126014501 | 12601450 | 1 | I | 20120207 | 0 | 20160727 | 20160727 | DIR | 44.00 | YR | F | N | 125.00000 | LBS | 20160726 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126014501 | 12601450 | 1 | PS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | N | D | 0 | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126014501 | 12601450 | 1 | Sinusitis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126014501 | 12601450 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126014501 | 12601450 | Arthralgia | |
126014501 | 12601450 | Dry eye | |
126014501 | 12601450 | Dysuria | |
126014501 | 12601450 | Fibromyalgia | |
126014501 | 12601450 | Myalgia | |
126014501 | 12601450 | Myasthenia gravis | |
126014501 | 12601450 | Neuropathy peripheral | |
126014501 | 12601450 | Systemic lupus erythematosus |
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 |
---|---|---|---|---|---|---|
126014501 | 12601450 | 1 | 20080207 | 20080209 | 0 |