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
125840852 12584085 2 F 20160714 20160722 20160728 EXP DE-BAYER-2016-138776 BAYER 0.00 F Y 0.00000 20160728 CN DE DE

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
125840852 12584085 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK 19537
125840852 12584085 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 19537

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125840852 12584085 1 Urinary tract inflammation
125840852 12584085 2 Pyelonephritis

Outcome of event

Event ID CASEID OUTC COD
125840852 12584085 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125840852 12584085 Alopecia
125840852 12584085 Arthropathy
125840852 12584085 Bone disorder
125840852 12584085 Bronchitis
125840852 12584085 Chest discomfort
125840852 12584085 Cognitive disorder
125840852 12584085 Fatigue
125840852 12584085 Gastrointestinal fungal infection
125840852 12584085 Headache
125840852 12584085 Immunodeficiency
125840852 12584085 Malaise
125840852 12584085 Mental disorder
125840852 12584085 Muscle atrophy
125840852 12584085 Onychoclasis
125840852 12584085 Oropharyngeal pain
125840852 12584085 Tendon disorder
125840852 12584085 Vulvovaginal candidiasis
125840852 12584085 Weight decreased

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
125840852 12584085 1 201507 0