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
126926681 12692668 1 I 2013 20160816 20160829 20160829 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122703 RANBAXY 0.00 M Y 0.00000 20160829 OT 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
126926681 12692668 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Intravenous (not otherwise specified) UNKNOWN U 75747
126926681 12692668 2 C INSULIN INSULIN NOS 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126926681 12692668 1 Nosocomial infection
126926681 12692668 2 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126926681 12692668 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126926681 12692668 Malaise
126926681 12692668 Musculoskeletal stiffness
126926681 12692668 Neuropathy peripheral
126926681 12692668 Pain
126926681 12692668 Retinal disorder
126926681 12692668 Tendon rupture
126926681 12692668 Tendonitis
126926681 12692668 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
126926681 12692668 1 2013 2013 0