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
126407881 12640788 1 I 20160504 20160804 20160810 20160810 EXP CN-MUNDIPHARMA DS AND PHARMACOVIGILANCE-GBR-2016-0039586 PURDUE 76.11 YR M Y 0.00000 20160809 OT CN CN

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
126407881 12640788 1 PS Oxycodone HCL PR Tablet OXYCODONE HYDROCHLORIDE 1 Oral 40 MG, DAILY 750 MG Y Y 184365 22272 40 MG PROLONGED-RELEASE TABLET
126407881 12640788 2 SS Oxycodone HCL PR Tablet OXYCODONE HYDROCHLORIDE 1 Oral 30 MG, DAILY 750 MG Y Y 184826 22272 30 MG PROLONGED-RELEASE TABLET
126407881 12640788 3 SS Oxycodone HCL PR Tablet OXYCODONE HYDROCHLORIDE 1 Oral UNK 750 MG Y Y 184826 22272 PROLONGED-RELEASE TABLET
126407881 12640788 4 SS Oxycodone HCL PR Tablet OXYCODONE HYDROCHLORIDE 1 Oral 10 MG, DAILY 750 MG Y Y 184826 22272 10 MG PROLONGED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126407881 12640788 1 Cancer pain

Outcome of event

Event ID CASEID OUTC COD
126407881 12640788 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126407881 12640788 Apnoea
126407881 12640788 Delirium
126407881 12640788 Feeling jittery
126407881 12640788 Hallucination

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
126407881 12640788 1 20160501 20160523 0
126407881 12640788 2 20160427 20160523 0
126407881 12640788 4 20160427 0