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
126670201 12667020 1 I 20151215 20160805 20160819 20160819 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122189 RANBAXY 69.00 YR M Y 78.00000 KG 20160819 OT 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
126670201 12667020 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, BID Y U 75747 500 MG Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126670201 12667020 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126670201 12667020 OT
126670201 12667020 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126670201 12667020 Anxiety
126670201 12667020 Arthralgia
126670201 12667020 Depression
126670201 12667020 Fatigue
126670201 12667020 Heart rate irregular
126670201 12667020 Hypoaesthesia
126670201 12667020 Myalgia
126670201 12667020 Pain
126670201 12667020 Paraesthesia
126670201 12667020 Photophobia
126670201 12667020 Rash
126670201 12667020 Suicidal ideation
126670201 12667020 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
126670201 12667020 1 201511 20151123 0