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
126523691 12652369 1 I 20160706 20160809 20160815 20160815 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201608-004026 CONCORDIA 68.00 YR M Y 0.00000 20160815 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
126523691 12652369 1 PS DIGOXIN. DIGOXIN 1 Y U 20405
126523691 12652369 2 SS DIGOXIN. DIGOXIN 1 Y U 20405
126523691 12652369 3 C FUROSEMIDE. FUROSEMIDE 1 0 40 MG QD
126523691 12652369 4 C FUROSEMIDE. FUROSEMIDE 1 0 80 MG QD
126523691 12652369 5 C RAMIPRIL. RAMIPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126523691 12652369 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126523691 12652369 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126523691 12652369 Agitation
126523691 12652369 Condition aggravated
126523691 12652369 Dizziness
126523691 12652369 Hypertension
126523691 12652369 Hypotension
126523691 12652369 Lethargy
126523691 12652369 Malaise
126523691 12652369 Night sweats
126523691 12652369 Panic attack

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found