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
127877191 12787719 1 I 20160919 20160928 20160928 EXP GB-MHRA-EYC 00145273 GB-CONCORDIA PHARMACEUTICALS INC.-GSH201609-004728 CONCORDIA 97.00 YR F Y 0.00000 20160928 OT GB GB

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
127877191 12787719 1 PS DIGOXIN. DIGOXIN 1 Oral Y U 20405
127877191 12787719 2 C BUMETANIDE. BUMETANIDE 1 0
127877191 12787719 3 C BUPRENORPHINE. BUPRENORPHINE 1 0
127877191 12787719 4 C FERROUS FUMARATE FERROUS FUMARATE 1 0
127877191 12787719 5 C RABEPRAZOLE RABEPRAZOLE 1 0
127877191 12787719 6 C RAMIPRIL. RAMIPRIL 1 0
127877191 12787719 7 C CALCICHEW D3 FORTE CALCIUMCHOLECALCIFEROL 1 0
127877191 12787719 8 C PARACETAMOL ACETAMINOPHEN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127877191 12787719 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127877191 12787719 Bradycardia

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
127877191 12787719 1 201606 20160908 0