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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127080841 | 12708084 | 1 | I | 2013 | 20160822 | 20160901 | 20160901 | EXP | US-INDIVIOR LIMITED-INDV-094232-2016 | INDIVIOR | 0.00 | A | F | Y | 0.00000 | 20160901 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127080841 | 12708084 | 1 | PS | SUBOXONE | BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE | 1 | Sublingual | DOSE RANGED FROM 2-16 MG/DAILY | Y | U | UNKNOWN | 20733 | TABLET | ||||||
127080841 | 12708084 | 2 | SS | SUBOXONE | BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE | 1 | Sublingual | DOSE RANGED FROM 2-16 MG/DAILY | Y | U | UNKNOWN | 0 | |||||||
127080841 | 12708084 | 3 | SS | SUBUTEX | BUPRENORPHINE HYDROCHLORIDE | 1 | Sublingual | DOSE RANGED FROM 2-16 MG/DAILY | Y | U | UNKNOWN | 0 | SUBLINGUAL TABLET | ||||||
127080841 | 12708084 | 4 | SS | Buprenorphine/Naloxone Generic | BUPRENORPHINENALOXONE | 1 | Sublingual | DOSE RANGED FROM 2-16 MG/DAILY | Y | U | UNKNOWN | 0 | |||||||
127080841 | 12708084 | 5 | SS | BUTRANS | BUPRENORPHINE | 1 | Transdermal | UNK | Y | U | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127080841 | 12708084 | 1 | Drug dependence |
127080841 | 12708084 | 2 | Drug dependence |
127080841 | 12708084 | 3 | Drug dependence |
127080841 | 12708084 | 4 | Drug dependence |
127080841 | 12708084 | 5 | Drug dependence |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127080841 | 12708084 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127080841 | 12708084 | Activities of daily living impaired | |
127080841 | 12708084 | Demyelination | |
127080841 | 12708084 | Fatigue | |
127080841 | 12708084 | Intentional underdose | |
127080841 | 12708084 | Multiple sclerosis | |
127080841 | 12708084 | Seizure | |
127080841 | 12708084 | Thinking abnormal | |
127080841 | 12708084 | Weight increased |
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 |
---|---|---|---|---|---|---|
127080841 | 12708084 | 1 | 2005 | 0 | ||
127080841 | 12708084 | 2 | 2013 | 2015 | 0 | |
127080841 | 12708084 | 5 | 2015 | 20150815 | 0 |