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
127437772 12743777 2 F 20150912 20160905 20160914 20160914 EXP PHHY2016IT122594 SANDOZ 86.39 YR F Y 0.00000 20160914 OT IT IT

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
127437772 12743777 1 PS AMIODARONE AMIODARONE 1 Oral 200 MG, QD 86000 MG Y 75315 200 MG QD
127437772 12743777 2 SS XARELTO RIVAROXABAN 1 Oral 15 MG, QD 6450 MG 0 15 MG FILM-COATED TABLET QD
127437772 12743777 3 C SIMVASTATIN. SIMVASTATIN 1 Unknown 20 MG, UNK U 0 20 MG
127437772 12743777 4 C ALPRAZOLAM. ALPRAZOLAM 1 Unknown 12 GTT, UNK Y 0 12 GTT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127437772 12743777 1 Atrial fibrillation
127437772 12743777 2 Atrial fibrillation
127437772 12743777 3 Arteriosclerosis coronary artery
127437772 12743777 4 Insomnia

Outcome of event

Event ID CASEID OUTC COD
127437772 12743777 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127437772 12743777 Hyperthyroidism
127437772 12743777 Normochromic normocytic anaemia

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
127437772 12743777 1 20140710 20150912 0
127437772 12743777 2 20140710 20150912 0