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
124556124 12455612 4 F 20160517 20160823 20160610 20160829 PER US-PFIZER INC-2016264077 PFIZER 81.00 YR M Y 70.31000 KG 20160829 OT 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
124556124 12455612 1 PS TIKOSYN DOFETILIDE 1 500 UG, 2X/DAY N21847 20931 500 UG CAPSULE, HARD BID
124556124 12455612 2 SS TIKOSYN DOFETILIDE 1 UNK N21847 20931 CAPSULE, HARD
124556124 12455612 3 C LISINOPRIL. LISINOPRIL 1 UNK 0
124556124 12455612 4 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK 0
124556124 12455612 5 C PRAVASTATIN. PRAVASTATIN 1 UNK 0
124556124 12455612 6 C XARELTO RIVAROXABAN 1 UNK 0
124556124 12455612 7 C VESICARE SOLIFENACIN SUCCINATE 1 UNK 0
124556124 12455612 8 C CIALIS TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124556124 12455612 1 Atrial flutter
124556124 12455612 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
124556124 12455612 HO
124556124 12455612 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124556124 12455612 Atrial fibrillation
124556124 12455612 Atrial flutter
124556124 12455612 Heart rate abnormal
124556124 12455612 Palpitations
124556124 12455612 Poor quality drug administered
124556124 12455612 Suspected counterfeit product

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
124556124 12455612 1 20150108 0