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
114718133 11471813 3 F 20160720 20150908 20160803 PER US-BAYER-2015-410938 BAYER 66.00 YR E M Y 64.41000 KG 20160803 CN US US

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
114718133 11471813 1 PS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 19537 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114718133 11471813 1 Prostate infection

Outcome of event

Event ID CASEID OUTC COD
114718133 11471813 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114718133 11471813 Coordination abnormal
114718133 11471813 Depressed mood
114718133 11471813 Emotional distress
114718133 11471813 Feeling abnormal
114718133 11471813 Gait disturbance
114718133 11471813 Initial insomnia
114718133 11471813 Injury
114718133 11471813 Insomnia
114718133 11471813 Limb discomfort
114718133 11471813 Mobility decreased
114718133 11471813 Neuropathy peripheral
114718133 11471813 Pain
114718133 11471813 Paraesthesia
114718133 11471813 Toxic neuropathy
114718133 11471813 Unevaluable event

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
114718133 11471813 1 20101117 20101127 0