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
110240806 11024080 6 F 200808 20160720 20150413 20160907 PER US-JNJFOC-20100802885 JANSSEN 49.13 YR A M Y 104.33000 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
110240806 11024080 1 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG UNSPECIFIED
110240806 11024080 2 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG UNSPECIFIED
110240806 11024080 3 PS LEVAQUIN LEVOFLOXACIN 1 Oral U U 20634 500 MG UNSPECIFIED
110240806 11024080 4 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown U 0 500 MG UNSPECIFIED
110240806 11024080 5 C AMOXICILLIN. AMOXICILLIN 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110240806 11024080 1 Pneumonia
110240806 11024080 2 Sinusitis
110240806 11024080 3 Bacterial infection
110240806 11024080 4 Bacterial infection
110240806 11024080 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
110240806 11024080 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110240806 11024080 Musculoskeletal pain
110240806 11024080 Neuropathy peripheral
110240806 11024080 Psychiatric symptom
110240806 11024080 Tendon injury

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
110240806 11024080 1 200808 0
110240806 11024080 2 200808 0
110240806 11024080 3 200808 0
110240806 11024080 4 200808 0