The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
4390412 4154183 F 1 4390412-7 20040401 20040616 20040630 EXP USA-2004-0013977 PURDUE PHARMA L.P. 48 YR M N 76.2 KG 20040629 MD 20040419

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
4390412 1004989431 PS OXYCONTIN 1 ORAL SEE IMAGE D D 20553
4390412 1005005644 SS BENZODIAZEPINE DERIVATIVES() 2 D D
4390412 1005005646 SS TRAMADOL HCL 1 D D
4390412 1005005649 SS OXYMORPHONE HYDROCHLORIDE 1 D D
4390412 1005005650 C ULTRAM 1
4390412 1005005653 C CELEBREX 1
4390412 1005005654 C SOMA 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4390412 1004989431 PAIN

Outcome of event

Event ID OUTC COD
4390412 DE
4390412 OT

Reactions reported

Event ID PT
4390412 ACCIDENTAL OVERDOSE
4390412 CARDIAC ARREST
4390412 CIRCULATORY COLLAPSE
4390412 DRUG DEPENDENCE
4390412 MALAISE
4390412 NAUSEA

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4390412 HP
4390412 OTH
4390412 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4390412 1004989431 20030710 20040220
4390412 1004989431 20040408