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
126102651 12610265 1 I 20160720 20160801 20160801 EXP GB-MHRA-ADR 23564272 GB-TEVA-679659ACC TEVA 81.00 YR M Y 0.00000 20160801 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
126102651 12610265 1 SS CODEINE CODEINE 1 Oral 240 MILLIGRAM DAILY; REQUIRED DOSE 30MG FOUR TIMES A DAY.390MG ADMINISTERED IN TOTAL. Y U 0 60 MG TABLET QID
126102651 12610265 2 PS MORPHINE MORPHINE 1 Y U 202718 5 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126102651 12610265 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102651 12610265 Aspiration
126102651 12610265 Cardiac disorder
126102651 12610265 Depressed level of consciousness
126102651 12610265 Drug administration error
126102651 12610265 Hypoxia
126102651 12610265 Renal failure
126102651 12610265 Shock
126102651 12610265 Unresponsive to stimuli
126102651 12610265 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
126102651 12610265 1 20160314 20160315 0
126102651 12610265 2 20160314 20160315 0