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
123683962 12368396 2 F 20160402 20160620 20160513 20160718 PER US-PFIZER INC-2016214358 PFIZER 75.00 YR M Y 95.25000 KG 20160718 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
123683962 12368396 1 PS TIKOSYN DOFETILIDE 1 Oral 375 UG, 2X/DAY 20931 375 UG CAPSULE, HARD BID
123683962 12368396 2 C METOPROLOL. METOPROLOL 1 50 MG, 2X/DAY 0 50 MG BID
123683962 12368396 3 C COUMADIN WARFARIN SODIUM 1 3.75MG ON MONDAY, 2.5MG EVERY DAY 0
123683962 12368396 4 C ATORVASTATIN ATORVASTATIN 1 40 MG, UNK 0 40 MG
123683962 12368396 5 C MAGNESIUM MAGNESIUM 1 400 MG, UNK 0 400 MG
123683962 12368396 6 C BABY ASPIRIN ASPIRIN 1 81 MG, 1X/DAY 0 81 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123683962 12368396 1 Atrial fibrillation
123683962 12368396 2 Blood pressure management
123683962 12368396 3 Cerebrovascular accident
123683962 12368396 4 Blood cholesterol
123683962 12368396 5 Mineral supplementation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123683962 12368396 Fall

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
123683962 12368396 1 20151201 0
123683962 12368396 2 201107 0
123683962 12368396 3 2005 0
123683962 12368396 4 1986 0
123683962 12368396 5 20151201 0
123683962 12368396 6 201107 0