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
122708993 12270899 3 F 20160718 20160415 20160725 EXP US-NAPPMUNDI-USA-2016-0130232 PURDUE 0.00 M Y 72.11000 KG 20160722 CN US US

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
122708993 12270899 1 PS OXYCONTIN OXYCODONE HYDROCHLORIDE 1 Oral 80 MG, TID U U UNKNOWN 22272 80 MG PROLONGED-RELEASE TABLET
122708993 12270899 2 SS Oxycodone Hydrochloride (similar to NDA 22-272) OXYCODONE HYDROCHLORIDE 1 Oral 30 MG, UNK U U UNKNOWN 0 30 MG
122708993 12270899 3 SS XANAX ALPRAZOLAM 1 Oral U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122708993 12270899 1 Product used for unknown indication
122708993 12270899 2 Product used for unknown indication
122708993 12270899 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122708993 12270899 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
122708993 12270899 Hypertensive heart disease
122708993 12270899 Intentional product use issue
122708993 12270899 Toxicity to various agents

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

no results found

Therapies reported

no results found