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
125216291 12521629 1 I 20160625 20160627 20160701 20160701 EXP US-INDIVIOR LIMITED-INDV-091771-2016 INDIVIOR 0.00 M Y 0.00000 20160701 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
125216291 12521629 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 24MG, DAILY Y U UNKNOWN 22410
125216291 12521629 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual CUT THE FILM AND TAPER HIS DOSE, UNK Y U UNKNOWN 22410
125216291 12521629 3 SS Buprenorphine/Naloxone Generic BUPRENORPHINENALOXONE 1 Sublingual 2MG, TWICE A DAY UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125216291 12521629 1 Drug dependence
125216291 12521629 3 Drug dependence

Outcome of event

Event ID CASEID OUTC COD
125216291 12521629 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125216291 12521629 Condition aggravated
125216291 12521629 Drug intolerance
125216291 12521629 Emphysema
125216291 12521629 Head discomfort
125216291 12521629 Product preparation error

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
125216291 12521629 1 201407 0
125216291 12521629 2 20160624 0
125216291 12521629 3 20160625 0