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
126620991 12662099 1 I 20151215 20160806 20160817 20160817 EXP GB-MHRA-EYC 00143216 GB-TEVA-683480ACC TEVA 69.00 YR M Y 78.00000 KG 20160817 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
126620991 12662099 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 1000 MILLIGRAM DAILY; Y U 74124 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126620991 12662099 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126620991 12662099 OT
126620991 12662099 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126620991 12662099 Anxiety
126620991 12662099 Arthralgia
126620991 12662099 Depression
126620991 12662099 Fatigue
126620991 12662099 Heart rate irregular
126620991 12662099 Hypoaesthesia
126620991 12662099 Myalgia
126620991 12662099 Pain
126620991 12662099 Paraesthesia
126620991 12662099 Photophobia
126620991 12662099 Rash
126620991 12662099 Suicidal ideation
126620991 12662099 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
126620991 12662099 1 201511 20151123 0