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
126066311 12606631 1 I 20160720 20160729 20160729 EXP GB-MUNDIPHARMA DS AND PHARMACOVIGILANCE-GBR-2016-0039253 PURDUE 81.00 YR M Y 0.00000 20160722 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
126066311 12606631 1 PS MORPHINE SULFATE. MORPHINE SULFATE 1 Unknown 5 MG, UNK Y U 2147483647 5 MG
126066311 12606631 2 SS CODEINE CODEINE 1 Oral 60 MG, QID Y U 0 60 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126066311 12606631 1 Product used for unknown indication
126066311 12606631 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126066311 12606631 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126066311 12606631 Aspiration
126066311 12606631 Cardiac disorder
126066311 12606631 Depressed level of consciousness
126066311 12606631 Drug administration error
126066311 12606631 Hypoxia
126066311 12606631 Renal failure
126066311 12606631 Shock
126066311 12606631 Unresponsive to stimuli
126066311 12606631 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
126066311 12606631 1 20160314 20160315 0
126066311 12606631 2 20160314 20160315 0