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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119188652 | 11918865 | 2 | F | 200604 | 20160720 | 20160115 | 20160907 | PER | US-JNJFOC-20151205056 | JANSSEN | 39.91 | YR | A | M | Y | 76.66000 | KG | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119188652 | 11918865 | 1 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | U | U | 0 | 500 | MG | TABLETS | ||||||
119188652 | 11918865 | 2 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | U | U | 0 | 500 | MG | TABLETS | ||||||
119188652 | 11918865 | 3 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | U | U | 0 | 500 | MG | TABLETS | ||||||
119188652 | 11918865 | 4 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | U | U | 0 | 500 | MG | TABLETS | ||||||
119188652 | 11918865 | 5 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | U | U | 0 | 500 | MG | TABLETS | ||||||
119188652 | 11918865 | 6 | PS | LEVAQUIN | LEVOFLOXACIN | 1 | Oral | U | U | 20634 | 500 | MG | TABLETS | ||||||
119188652 | 11918865 | 7 | SS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Unknown | U | 0 | 500 | MG | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
119188652 | 11918865 | 1 | Dysuria |
119188652 | 11918865 | 2 | Dysuria |
119188652 | 11918865 | 3 | Haematuria |
119188652 | 11918865 | 4 | Haematuria |
119188652 | 11918865 | 5 | Prostatitis |
119188652 | 11918865 | 6 | Prostatitis |
119188652 | 11918865 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
119188652 | 11918865 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
119188652 | 11918865 | Drug hypersensitivity | |
119188652 | 11918865 | Neuropathy peripheral |
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 |
---|---|---|---|---|---|---|
119188652 | 11918865 | 1 | 20060420 | 0 | ||
119188652 | 11918865 | 2 | 20030729 | 0 | ||
119188652 | 11918865 | 3 | 20030729 | 0 | ||
119188652 | 11918865 | 4 | 20060420 | 0 | ||
119188652 | 11918865 | 5 | 20060420 | 0 | ||
119188652 | 11918865 | 6 | 20030729 | 0 | ||
119188652 | 11918865 | 7 | 20030712 | 0 |