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
125699941 12569994 1 I 20160125 20160708 20160719 20160719 EXP FR-INDIVIOR LIMITED-INDV-092175-2016 INDIVIOR 25.35 YR M Y 0.00000 20160719 OT FR FR

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
125699941 12569994 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Unknown 8 MG, QD U UNKNOWN 20732 8 MG SUBLINGUAL TABLET QD
125699941 12569994 2 SS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Oral ALMOST 16MG, UNK U UNKNOWN 20732 SUBLINGUAL TABLET
125699941 12569994 3 SS VALIUM DIAZEPAM 1 Unknown 10MG TABLET,5 TIMES A DAY U 0
125699941 12569994 4 SS VALIUM DIAZEPAM 1 Unknown 10MG TABLET,5 TIMES A DAY U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125699941 12569994 1 Overdose
125699941 12569994 3 Overdose

Outcome of event

Event ID CASEID OUTC COD
125699941 12569994 HO
125699941 12569994 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125699941 12569994 Coma
125699941 12569994 Disturbance in attention
125699941 12569994 Hyperhidrosis
125699941 12569994 Mydriasis
125699941 12569994 Seizure
125699941 12569994 Somnolence
125699941 12569994 Toxicity to various agents

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
125699941 12569994 2 20160125 0
125699941 12569994 4 20160125 0