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
125261391 12526139 1 I 20160630 0 20160701 20160701 DIR 39.00 YR F N 125.00000 LBS 20160630 N 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
125261391 12526139 1 PS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Sublingual Y D A16GW108 20170630 0 60 DF BID
125261391 12526139 2 C CELEXA CITALOPRAM HYDROBROMIDE 1 0
125261391 12526139 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
125261391 12526139 4 C NIFEDIPINE. NIFEDIPINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125261391 12526139 1 Drug dependence

Outcome of event

Event ID CASEID OUTC COD
125261391 12526139 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125261391 12526139 Blood pressure increased
125261391 12526139 Impaired work ability
125261391 12526139 Peripheral swelling
125261391 12526139 Raynaud's phenomenon
125261391 12526139 Skin discolouration
125261391 12526139 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
125261391 12526139 1 20160301 20160620 0