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
126676151 12667615 1 I 201608 20160812 20160819 20160819 EXP US-INDIVIOR LIMITED-INDV-093793-2016 INDIVIOR 38.00 YR F Y 0.00000 20160819 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
126676151 12667615 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 8 MG, BID, FOR ABOUT FIVE YEARS Y UNKNOWN 22410 8 MG BID
126676151 12667615 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Unknown UNK U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126676151 12667615 1 Drug dependence
126676151 12667615 2 Drug withdrawal syndrome

Outcome of event

Event ID CASEID OUTC COD
126676151 12667615 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126676151 12667615 Decreased appetite
126676151 12667615 Drug withdrawal syndrome
126676151 12667615 Insomnia
126676151 12667615 Intentional product misuse
126676151 12667615 Loss of consciousness
126676151 12667615 Panic attack
126676151 12667615 Substance abuse
126676151 12667615 Therapy cessation
126676151 12667615 Weight decreased

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
126676151 12667615 1 20160801 0
126676151 12667615 2 201608 0