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
100428413 10042841 3 F 2013 20160901 20140327 20160909 EXP US-RB-063816-14 INDIVIOR 42.00 YR M Y 0.00000 20160909 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
100428413 10042841 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 24MG, DAILY UNKNOWN 22410
100428413 10042841 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 16MG DAILY, TAKING LESS THAN PRESCRIBED UNKNOWN 22410
100428413 10042841 3 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 Oral DOSING DETAILS UNKNOWN 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100428413 10042841 1 Drug dependence
100428413 10042841 3 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
100428413 10042841 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100428413 10042841 Condition aggravated
100428413 10042841 Dehydration
100428413 10042841 Hepatic cancer
100428413 10042841 Hepatic cirrhosis
100428413 10042841 Hepatitis C
100428413 10042841 Intentional underdose
100428413 10042841 Nausea
100428413 10042841 Tooth malformation
100428413 10042841 Vomiting

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
100428413 10042841 1 2011 2013 0
100428413 10042841 2 2013 0
100428413 10042841 3 2008 0