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
125374161 12537416 1 I 2014 20160628 20160707 20160707 EXP CH-INDIVIOR LIMITED-INDV-091804-2016 INDIVIOR 0.00 F Y 0.00000 20160707 MD CH CH

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
125374161 12537416 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Unknown 4 MG, UNK UNKNOWN 20732 4 MG SUBLINGUAL TABLET
125374161 12537416 2 SS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Unknown 2 MG, UNK UNKNOWN 20732 2 MG SUBLINGUAL TABLET QD
125374161 12537416 3 SS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Unknown 4 MG, UNK UNKNOWN 20732 4 MG SUBLINGUAL TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125374161 12537416 1 Substance dependence

Outcome of event

Event ID CASEID OUTC COD
125374161 12537416 OT
125374161 12537416 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125374161 12537416 Maternal exposure during pregnancy
125374161 12537416 Mycoplasma infection
125374161 12537416 Urinary tract infection
125374161 12537416 Vulvovaginal injury

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
125374161 12537416 1 2012 0
125374161 12537416 2 2014 2015 0