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
126948131 12694813 1 I 2015 20160818 20160829 20160829 EXP US-INDIVIOR LIMITED-INDV-094179-2016 INDIVIOR 55.00 YR M Y 0.00000 20160829 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
126948131 12694813 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual 2 MG, FOUR TIMES A DAY, BY CUTTING Y UNKNOWN 22410
126948131 12694813 2 C PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral UNK 0
126948131 12694813 3 C ATIVAN LORAZEPAM 1 Oral 2 MG, TWICE A DAY 0
126948131 12694813 4 C ATIVAN LORAZEPAM 1 Oral 3 MG, TWICE A DAY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126948131 12694813 1 Drug dependence
126948131 12694813 2 Post-traumatic stress disorder
126948131 12694813 3 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126948131 12694813 HO
126948131 12694813 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126948131 12694813 Diarrhoea
126948131 12694813 Fatigue
126948131 12694813 Hyperhidrosis
126948131 12694813 Intentional product misuse
126948131 12694813 Oral discomfort
126948131 12694813 Oral pain
126948131 12694813 Procedural pain
126948131 12694813 Product preparation error
126948131 12694813 Small intestine carcinoma
126948131 12694813 Umbilical hernia

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
126948131 12694813 1 2015 201602 0
126948131 12694813 3 201608 0
126948131 12694813 4 201608 0