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
121321142 12132114 2 F 20070123 20160720 20160301 20160907 PER US-JNJFOC-20160207904 JANSSEN 60.34 YR A M Y 96.62000 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
121321142 12132114 1 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
121321142 12132114 2 SS LEVAQUIN LEVOFLOXACIN 1 Oral U U 0 500 MG TABLETS
121321142 12132114 3 PS LEVAQUIN LEVOFLOXACIN 1 Oral U U 20634 500 MG TABLETS
121321142 12132114 4 SS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 Oral U 0 500 MG UNSPECIFIED
121321142 12132114 5 SS MOXIFLOXACIN. MOXIFLOXACIN 1 Oral U 0 UNSPECIFIED
121321142 12132114 6 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121321142 12132114 1 Chills
121321142 12132114 2 Pyrexia
121321142 12132114 3 Headache
121321142 12132114 4 Influenza like illness
121321142 12132114 5 Product used for unknown indication
121321142 12132114 6 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
121321142 12132114 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121321142 12132114 Drug hypersensitivity
121321142 12132114 Drug intolerance
121321142 12132114 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
121321142 12132114 1 20070123 20070130 0
121321142 12132114 2 20070123 20070130 0
121321142 12132114 3 20070123 20070130 0
121321142 12132114 4 20070115 0
121321142 12132114 6 2008 0