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
126851521 12685152 1 I 2011 20160815 20160825 20160825 EXP US-INDIVIOR LIMITED-INDV-093861-2016 INDIVIOR 0.00 A F Y 0.00000 20160825 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
126851521 12685152 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 2 MG, 5 TIMES/DAY UNKNOWN 22410 2 MG
126851521 12685152 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual UNKNOWN, ABOUT 1 YEAR Y U UNKNOWN 0 TABLET
126851521 12685152 3 SS BUTRANS BUPRENORPHINE 1 Transdermal UNK Y U UNKNOWN 0
126851521 12685152 4 SS Buprenorphine/Naloxone Generic BUPRENORPHINENALOXONE 1 Sublingual 2 MG, FIVE TIMES A DAY Y U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126851521 12685152 1 Pain
126851521 12685152 2 Pain
126851521 12685152 3 Pain
126851521 12685152 4 Pain

Outcome of event

Event ID CASEID OUTC COD
126851521 12685152 HO
126851521 12685152 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126851521 12685152 Hand fracture
126851521 12685152 Hypoaesthesia oral
126851521 12685152 Intentional product misuse
126851521 12685152 Off label use
126851521 12685152 Oral mucosal blistering

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
126851521 12685152 1 2015 0
126851521 12685152 2 2011 2012 0
126851521 12685152 3 2012 201408 0
126851521 12685152 4 201505 2015 0