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
125416791 12541679 1 I 20160501 20160630 20160708 20160708 EXP FR-PURDUE PHARMA-GBR-2016-0037709 PURDUE 85.85 YR F Y 0.00000 20160708 OT FR FR

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
125416791 12541679 1 PS OXYCONTIN OXYCODONE HYDROCHLORIDE 1 Unknown 1 DF, BID U U 22272 1 DF PROLONGED-RELEASE TABLET
125416791 12541679 2 SS OXYNORM 5 mg, gelule OXYCODONE HYDROCHLORIDE 1 Unknown 1 DF, DAILY U U 0 1 DF CAPSULE, HARD
125416791 12541679 3 SS AMLOR AMLODIPINE BESYLATE 1 Oral 1 DF, DAILY U U 0 1 DF
125416791 12541679 4 SS RAMIPRIL. RAMIPRIL 1 Oral 1 DF, DAILY Y U 0 1 DF
125416791 12541679 5 SS SERESTA OXAZEPAM 1 Oral 1 DF, DAILY U U 0 1 DF
125416791 12541679 6 C ESIDREX HYDROCHLOROTHIAZIDE 1 1 DF, DAILY U 0 1 DF
125416791 12541679 7 C CLINUTREN 2 UNK, BID U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125416791 12541679 1 Pain
125416791 12541679 2 Pain
125416791 12541679 3 Hypertension
125416791 12541679 4 Hypertension
125416791 12541679 5 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125416791 12541679 OT
125416791 12541679 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125416791 12541679 Acute kidney injury
125416791 12541679 Malaise

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
125416791 12541679 1 201604 20160501 0
125416791 12541679 2 201604 20160501 0
125416791 12541679 3 201604 20160501 0
125416791 12541679 4 201604 20160501 0
125416791 12541679 5 201604 0