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
126635171 12663517 1 I 20151215 20160805 20160818 20160818 EXP GB-AUROBINDO-AUR-APL-2016-10305 AUROBINDO 69.00 YR M Y 78.00000 KG 20160818 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
126635171 12663517 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, TWO TIMES A DAY Y U 77859 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126635171 12663517 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126635171 12663517 DS
126635171 12663517 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126635171 12663517 Anxiety
126635171 12663517 Arthralgia
126635171 12663517 Depression
126635171 12663517 Fatigue
126635171 12663517 Heart rate irregular
126635171 12663517 Hypoaesthesia
126635171 12663517 Myalgia
126635171 12663517 Pain
126635171 12663517 Paraesthesia
126635171 12663517 Photophobia
126635171 12663517 Rash
126635171 12663517 Suicidal ideation
126635171 12663517 Tendon disorder

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
126635171 12663517 1 201511 20151123 0