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
127199552 12719955 2 F 2003 20160926 20160907 20160928 PER US-JNJFOC-20150810251 JANSSEN 0.00 A F Y 74.84000 KG 20160927 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
127199552 12719955 1 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS QD
127199552 12719955 2 PS LEVAQUIN LEVOFLOXACIN 1 Oral U U 20634 TABLETS
127199552 12719955 3 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Oral D 0 400 MG TABLETS QD
127199552 12719955 4 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Oral D 0 400 MG TABLETS QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127199552 12719955 1 Respiratory tract infection
127199552 12719955 2 Respiratory tract infection
127199552 12719955 3 Respiratory tract infection
127199552 12719955 4 Respiratory tract infection

Outcome of event

Event ID CASEID OUTC COD
127199552 12719955 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127199552 12719955 Amnesia
127199552 12719955 Depression
127199552 12719955 Gait disturbance
127199552 12719955 Neuropathy peripheral
127199552 12719955 Sleep disorder

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
127199552 12719955 1 20030915 20030925 0
127199552 12719955 2 200307 0
127199552 12719955 3 20001127 20001207 0
127199552 12719955 4 20020522 20020527 0