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
126922611 12692261 1 I 2013 20160816 20160828 20160828 EXP GB-MHRA-ADR 23598114 GB-TEVA-687186ACC TEVA 0.00 M Y 0.00000 20160829 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
126922611 12692261 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Intravenous (not otherwise specified) UNKNOWN U 74124
126922611 12692261 2 C INSULIN INSULIN NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126922611 12692261 1 Nosocomial infection
126922611 12692261 2 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126922611 12692261 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126922611 12692261 Malaise
126922611 12692261 Musculoskeletal stiffness
126922611 12692261 Neuropathy peripheral
126922611 12692261 Pain
126922611 12692261 Retinal disorder
126922611 12692261 Tendon rupture
126922611 12692261 Tendonitis
126922611 12692261 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
126922611 12692261 1 2013 2013 0