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
126905471 12690547 1 I 20100621 20160819 20160826 20160826 EXP US-PURDUE PHARMA-USA-2016-0133068 PURDUE 5.00 YR M Y 0.00000 20160826 MD 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
126905471 12690547 1 PS OXYCONTIN OXYCODONE HYDROCHLORIDE 1 Oral UNK U U UNKNOWN 22272 PROLONGED-RELEASE TABLET
126905471 12690547 2 SS Oxycodone Hydrochloride (similar to NDA 22-272) OXYCODONE HYDROCHLORIDE 1 Oral UNK U U UNKNOWN 0
126905471 12690547 3 SS LORTAB ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown UNK U U UNKNOWN 0
126905471 12690547 4 SS SOMA CARISOPRODOL 1 Unknown UNK U U UNKNOWN 0
126905471 12690547 5 SS XANAX ALPRAZOLAM 1 Unknown UNK U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126905471 12690547 1 Product used for unknown indication
126905471 12690547 2 Product used for unknown indication
126905471 12690547 3 Product used for unknown indication
126905471 12690547 4 Product used for unknown indication
126905471 12690547 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126905471 12690547 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126905471 12690547 Hypoxia
126905471 12690547 Loss of consciousness
126905471 12690547 Overdose

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

no results found

Therapies reported

no results found