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
126064051 12606405 1 I 20160520 20160715 20160729 20160729 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121117 RANBAXY 74.00 YR M Y 71.66000 KG 20160729 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
126064051 12606405 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 750 MG, BID 10500 MG N U 75747 750 MG Q12H
126064051 12606405 2 C DICLOFLEX 2 Unknown U U 0 75 MG
126064051 12606405 3 C ELIQUIS APIXABAN 1 Unknown U U 0 2.5 MG
126064051 12606405 4 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown U U 0 20 MG
126064051 12606405 5 C TAMSULOSIN TAMSULOSIN 1 Unknown U U 0 400 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126064051 12606405 1 Lung infection
126064051 12606405 2 Product used for unknown indication
126064051 12606405 3 Product used for unknown indication
126064051 12606405 4 Product used for unknown indication
126064051 12606405 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126064051 12606405 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126064051 12606405 Pain
126064051 12606405 Peripheral swelling
126064051 12606405 Swelling face

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
126064051 12606405 1 20160513 20160524 0