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
117418393 11741839 3 F 201010 20160803 20151116 20160816 EXP US-JNJFOC-20151108031 JANSSEN 48.72 YR A F Y 0.00000 20160816 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
117418393 11741839 1 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 TABLETS
117418393 11741839 2 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 TABLETS
117418393 11741839 3 PS LEVAQUIN LEVOFLOXACIN 1 Oral U U 20634 500 MG TABLETS QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117418393 11741839 1 Sinusitis
117418393 11741839 2 Sinusitis
117418393 11741839 3 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
117418393 11741839 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117418393 11741839 Nerve injury
117418393 11741839 Neuropathy peripheral
117418393 11741839 Tendonitis

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
117418393 11741839 1 20080815 20080824 0
117418393 11741839 2 20040123 20040202 0
117418393 11741839 3 20100930 20101004 0