The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
119189062 11918906 2 F 200710 20160720 20160115 20160907 PER US-JNJFOC-20151205106 JANSSEN 41.20 YR A F Y 71.67000 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
119189062 11918906 1 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
119189062 11918906 2 PS LEVAQUIN LEVOFLOXACIN 1 Oral U U 20634 500 MG TABLETS
119189062 11918906 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown 0 250 MG UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119189062 11918906 1 Sinusitis
119189062 11918906 2 Sinusitis
119189062 11918906 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119189062 11918906 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119189062 11918906 Arthralgia
119189062 11918906 Myalgia
119189062 11918906 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
119189062 11918906 1 20000513 20000518 0
119189062 11918906 2 20071022 20071101 0
119189062 11918906 3 20060614 0