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
125732471 12573247 1 I 20160705 20160720 20160720 EXP LB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120486 RANBAXY 54.00 YR F Y 0.00000 20160720 OT GB LB

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
125732471 12573247 1 SS IMIPENEM AND CILASTATIN CILASTATIN SODIUMIMIPENEM 1 Intravenous (not otherwise specified) 500 MG, TID U U 0 500 MG Q8H
125732471 12573247 2 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, BID Y U 75747 500 MG Q12H
125732471 12573247 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Intravenous (not otherwise specified) 400 MG, BID Y U 0 400 MG Q12H
125732471 12573247 4 SS Vancomycin VANCOMYCIN 1 Intravenous (not otherwise specified) 1 G, BID U U 0 1 G Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125732471 12573247 1 Colitis
125732471 12573247 2 Colitis
125732471 12573247 3 Colitis
125732471 12573247 4 Colitis

Outcome of event

Event ID CASEID OUTC COD
125732471 12573247 HO
125732471 12573247 LT
125732471 12573247 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125732471 12573247 Acute respiratory distress syndrome
125732471 12573247 Drug ineffective
125732471 12573247 Pathogen resistance
125732471 12573247 Septic shock

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found