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
126631751 12663175 1 I 20160720 20160806 20160818 20160818 EXP GB-MHRA-EYC 00143174 GB-TEVA-683467ACC TEVA 94.00 YR F Y 60.00000 KG 20160818 PH 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
126631751 12663175 1 PS BUMETANIDE. BUMETANIDE 1 DOSE INCREASED ON THIS DATE Y U 74225
126631751 12663175 2 SS DIGOXIN. DIGOXIN 1 Oral 125 MICROGRAM DAILY; 1250 UG Y U 0 125 UG QD
126631751 12663175 3 SS DIGOXIN. DIGOXIN 1 Oral LOADING DOSE 1250 UG Y U 0 1000 UG
126631751 12663175 4 C ATORVASTATIN ATORVASTATIN 1 0
126631751 12663175 5 C FERROUS FUMARATE FERROUS FUMARATE 1 0
126631751 12663175 6 C FOLIC ACID. FOLIC ACID 1 0
126631751 12663175 7 C PREGABALIN. PREGABALIN 1 0
126631751 12663175 8 C QUININE QUININE 1 HELD 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126631751 12663175 2 Atrial fibrillation
126631751 12663175 3 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126631751 12663175 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126631751 12663175 Acute kidney injury
126631751 12663175 Bradycardia
126631751 12663175 Confusional state
126631751 12663175 Incorrect dose administered
126631751 12663175 Toxicity to various agents

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
126631751 12663175 1 20160710 0
126631751 12663175 2 20160710 20160720 0