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
127203341 12720334 1 I 20160728 20160825 20160907 20160907 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123101 RANBAXY 80.00 YR M Y 64.00000 KG 20160907 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
127203341 12720334 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, BID 1000 MG Y U 75747 500 MG Q12H
127203341 12720334 2 C LISINOPRIL. LISINOPRIL 1 Unknown 10 MG, UNK U U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127203341 12720334 1 Urinary tract infection
127203341 12720334 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127203341 12720334 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127203341 12720334 Myositis
127203341 12720334 Pain
127203341 12720334 Rash
127203341 12720334 Tendonitis
127203341 12720334 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
127203341 12720334 1 20160728 20160816 0