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
126174891 12617489 1 I 20160720 20160803 20160803 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121163 RANBAXY 81.00 YR M Y 0.00000 20160803 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
126174891 12617489 1 SS Codeine CODEINE 1 Oral REQUIRED DOSE 30MG FOUR TIMES A DAY. 390MG ADMINISTERED IN TOTAL. Y U 0 60 MG Q6H
126174891 12617489 2 PS Morphine MORPHINE 1 Unknown 5 MG, UNK Y U 78761 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126174891 12617489 1 Product used for unknown indication
126174891 12617489 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126174891 12617489 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126174891 12617489 Aspiration
126174891 12617489 Cardiac disorder
126174891 12617489 Depressed level of consciousness
126174891 12617489 Drug administration error
126174891 12617489 Hypoxia
126174891 12617489 Renal failure
126174891 12617489 Shock
126174891 12617489 Unresponsive to stimuli
126174891 12617489 Vomiting

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
126174891 12617489 1 20160314 20160315 0
126174891 12617489 2 20160314 20160315 0