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
125376034 12537603 4 F 201604 20160728 20160707 20160805 PER US-PFIZER INC-2016320463 PFIZER 83.00 YR F Y 45.35000 KG 20160805 PH 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
125376034 12537603 1 PS TIKOSYN DOFETILIDE 1 Oral 0.25 MG, 2X/DAY 20931 .25 MG CAPSULE, HARD BID
125376034 12537603 2 SS ELIQUIS APIXABAN 1 Oral 2.5 MG, 2X/DAY (2.5MG BY MOUTH EVERY 12 HOURS) 0 2.5 MG FILM-COATED TABLET BID
125376034 12537603 3 SS SOTALOL. SOTALOL 1 80 MG, 2X/DAY Y 0 80 MG TABLET BID
125376034 12537603 4 C METOPROLOL. METOPROLOL 1 Oral 50 MG, 2X/DAY 0 50 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125376034 12537603 1 Atrial fibrillation
125376034 12537603 2 Cerebrovascular accident prophylaxis
125376034 12537603 3 Atrial fibrillation
125376034 12537603 4 Arrhythmia

Outcome of event

Event ID CASEID OUTC COD
125376034 12537603 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125376034 12537603 Atrial fibrillation
125376034 12537603 Headache
125376034 12537603 Nausea

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
125376034 12537603 1 20160615 0
125376034 12537603 2 201604 0
125376034 12537603 3 20160413 201606 0
125376034 12537603 4 2015 0