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
122821123 12282112 3 F 20160809 20160419 20160818 PER US-PFIZER INC-2016214212 PFIZER 70.00 YR F Y 73.00000 KG 20160818 CN US 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
122821123 12282112 1 PS TIKOSYN DOFETILIDE 1 Oral 500 UG, 2X/DAY 20931 500 UG CAPSULE, HARD BID
122821123 12282112 2 C XARELTO RIVAROXABAN 1 20 MG, 1X/DAY 0 20 MG QD
122821123 12282112 3 C XARELTO RIVAROXABAN 1 UNK 0
122821123 12282112 4 C LISINOPRIL. LISINOPRIL 1 2.5 MG, 1X/DAY 0 2.5 MG QD
122821123 12282112 5 C LISINOPRIL. LISINOPRIL 1 UNK 0
122821123 12282112 6 C LASIX FUROSEMIDE 1 20 MG, 1X/DAY 0 20 MG TABLET QD
122821123 12282112 7 C LASIX FUROSEMIDE 1 UNK 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122821123 12282112 1 Atrial fibrillation
122821123 12282112 2 Thrombosis prophylaxis
122821123 12282112 4 Blood pressure abnormal
122821123 12282112 6 Fluid retention

Outcome of event

Event ID CASEID OUTC COD
122821123 12282112 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122821123 12282112 Drug ineffective

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
122821123 12282112 1 20150410 0
122821123 12282112 2 201504 0
122821123 12282112 3 20120701 0
122821123 12282112 4 201503 0
122821123 12282112 5 20120701 0
122821123 12282112 6 201508 0
122821123 12282112 7 20150701 0