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
125798441 12579844 1 I 20160713 20160721 20160721 EXP FR-INDIVIOR LIMITED-INDV-092254-2016 INDIVIOR 42.00 YR M Y 0.00000 20160721 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
125798441 12579844 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Parenteral 8MG, ONCE DAILY IN THE MORNING, FOR 1 YEAR U UNKNOWN 20732 SUBLINGUAL TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125798441 12579844 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125798441 12579844 HO
125798441 12579844 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125798441 12579844 Drug abuse
125798441 12579844 Endocarditis
125798441 12579844 Intentional product use issue
125798441 12579844 Pulmonary embolism
125798441 12579844 Venous thrombosis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found