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
118303994 11830399 4 F 2011 20160720 20151214 20160907 PER US-JNJFOC-20111107139 JANSSEN 0.00 A F Y 0.00000 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
118303994 11830399 1 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
118303994 11830399 2 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
118303994 11830399 3 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
118303994 11830399 4 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
118303994 11830399 5 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
118303994 11830399 6 PS LEVAQUIN LEVOFLOXACIN 1 Oral U U 20634 500 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118303994 11830399 1 Sinusitis
118303994 11830399 2 Sinusitis
118303994 11830399 3 Sinusitis
118303994 11830399 4 Bacterial infection
118303994 11830399 5 Bacterial infection
118303994 11830399 6 Bacterial infection

Outcome of event

Event ID CASEID OUTC COD
118303994 11830399 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118303994 11830399 Neuropathy peripheral
118303994 11830399 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
118303994 11830399 1 20100204 20100214 0
118303994 11830399 2 20110407 20110423 0
118303994 11830399 3 20110222 20110306 0
118303994 11830399 4 20100204 20100214 0
118303994 11830399 5 20110407 20110423 0
118303994 11830399 6 20110222 20110306 0