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
117201233 11720123 3 F 20160816 20151110 20160824 EXP US-BAYER-2015-459193 BAYER 0.00 E F Y 90.70000 KG 20160825 MD 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
117201233 11720123 1 PS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 19537 TABLET
117201233 11720123 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 500 MG, BID 0 500 MG MODIFIED-RELEASE FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117201233 11720123 2 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
117201233 11720123 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117201233 11720123 Anxiety
117201233 11720123 Breast pain
117201233 11720123 Emotional distress
117201233 11720123 Headache
117201233 11720123 Injury
117201233 11720123 Neuropathy peripheral
117201233 11720123 Pain
117201233 11720123 Pain in extremity

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
117201233 11720123 2 20110526 20110601 0