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
120064963 12006496 3 F 2012 20160801 20160204 20160811 PER US-BAYER-2016-020744 BAYER 37.00 YR A F Y 91.61000 KG 20160811 OT 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
120064963 12006496 1 PS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 19537 TABLET
120064963 12006496 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 0 FILM-COATED TABLET
120064963 12006496 3 SS LEVAQUIN LEVOFLOXACIN 1 UNK 0
120064963 12006496 4 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, UNK 0 500 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
120064963 12006496 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120064963 12006496 Cardiovascular disorder
120064963 12006496 Mental disorder
120064963 12006496 Musculoskeletal injury
120064963 12006496 Nervous system disorder
120064963 12006496 Neuropathy peripheral
120064963 12006496 Pain
120064963 12006496 Skin injury

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
120064963 12006496 1 20120301 0
120064963 12006496 4 20120328 0