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
127674311 12767431 1 I 2012 20160914 20160921 20160921 EXP US-INDIVIOR LIMITED-INDV-094945-2016 INDIVIOR 0.00 E M Y 0.00000 20160921 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
127674311 12767431 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual UNK, DAILY UNKNOWN 22410
127674311 12767431 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual UNK, DAILY UNKNOWN 22410

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127674311 12767431 1 Drug dependence

Outcome of event

Event ID CASEID OUTC COD
127674311 12767431 OT
127674311 12767431 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127674311 12767431 Carbon dioxide increased
127674311 12767431 Cerebrovascular accident
127674311 12767431 Drug withdrawal syndrome
127674311 12767431 Hyperhidrosis
127674311 12767431 Pneumonia
127674311 12767431 Respiratory rate 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
127674311 12767431 2 2012 0