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
126782991 12678299 1 I 2013 20160816 20160823 20160823 EXP GB-MHRA-ADR 23598114 GB-MYLANLABS-2016M1034595 MYLAN 0.00 Y 0.00000 20160823 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
126782991 12678299 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Intravenous (not otherwise specified) UNKNOWN 75817
126782991 12678299 2 C INSULIN INSULIN NOS 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126782991 12678299 1 Nosocomial infection
126782991 12678299 2 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126782991 12678299 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126782991 12678299 Malaise
126782991 12678299 Musculoskeletal stiffness
126782991 12678299 Neuropathy peripheral
126782991 12678299 Pain
126782991 12678299 Retinal disorder
126782991 12678299 Tendon rupture
126782991 12678299 Tendonitis
126782991 12678299 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
126782991 12678299 1 2013 2013 0