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
125216462 12521646 2 F 20160425 20160630 20160701 20160708 EXP FI-INDIVIOR LIMITED-INDV-091721-2016 INDIVIOR 45.00 YR M Y 0.00000 20160708 MD FI FI

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
125216462 12521646 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 1 DOSAGE FORM (FILM), DAILY Y UNKNOWN 22410
125216462 12521646 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Unknown UNK U N UNKNOWN 0 TABLET
125216462 12521646 3 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 2 MG, UNK U N UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125216462 12521646 1 Drug dependence
125216462 12521646 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125216462 12521646 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125216462 12521646 Headache
125216462 12521646 Malaise
125216462 12521646 Mechanical urticaria

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
125216462 12521646 1 20160425 20160427 0
125216462 12521646 2 20160425 0
125216462 12521646 3 20160428 0