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
126901891 12690189 1 I 2013 20160816 20160826 20160826 EXP GB-MHRA-ADR 23598114 GB-WEST-WARD PHARMACEUTICALS CORP.-GB-H14001-16-01626 WESTWARD 0.00 M Y 0.00000 20160826 CN GB GB

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
126901891 12690189 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Intravenous (not otherwise specified) 76558
126901891 12690189 2 C INSULIN INSULIN NOS 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126901891 12690189 1 Nosocomial infection
126901891 12690189 2 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126901891 12690189 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126901891 12690189 Malaise
126901891 12690189 Musculoskeletal stiffness
126901891 12690189 Neuropathy peripheral
126901891 12690189 Pain
126901891 12690189 Retinal disorder
126901891 12690189 Tendon rupture
126901891 12690189 Tendonitis
126901891 12690189 Visual acuity reduced

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
126901891 12690189 1 2013 2013 0