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
127236531 12723653 1 I 20160728 20160825 20160908 20160908 EXP GB-AUROBINDO-AUR-APL-2016-10998 AUROBINDO 80.00 YR M Y 64.00000 KG 20160908 MD 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
127236531 12723653 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, TWO TIMES A DAY 1000 MG Y U 77859 500 MG BID
127236531 12723653 2 C LISINOPRIL. LISINOPRIL 1 Unknown 10 MG, UNK U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127236531 12723653 1 Urinary tract infection
127236531 12723653 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127236531 12723653 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127236531 12723653 Myositis
127236531 12723653 Pain
127236531 12723653 Rash
127236531 12723653 Tendonitis
127236531 12723653 White blood cell count increased

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
127236531 12723653 1 20160728 20160816 0