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
125694183 12569418 3 F 20160829 20160719 20160902 PER US-PFIZER INC-2016309699 PFIZER 88.00 YR F Y 0.00000 20160902 MD 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
125694183 12569418 1 PS TIKOSYN DOFETILIDE 1 20 MG, 1X/DAY Y 20931 20 MG CAPSULE, HARD QD
125694183 12569418 2 C ELIQUIS APIXABAN 1 UNK 0
125694183 12569418 3 C PLAVIX CLOPIDOGREL BISULFATE 1 UNK 0
125694183 12569418 4 C SPIRONOLACTONE. SPIRONOLACTONE 1 UNK 0
125694183 12569418 5 C TORSEMIDE. TORSEMIDE 1 UNK 0
125694183 12569418 6 C CARDIZEM DILTIAZEM HYDROCHLORIDE 1 UNK 0
125694183 12569418 7 C LISINOPRIL. LISINOPRIL 1 UNK 0
125694183 12569418 8 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK 0
125694183 12569418 9 C SLOAN 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125694183 12569418 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125694183 12569418 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125694183 12569418 Dizziness
125694183 12569418 Heart rate decreased
125694183 12569418 Weight increased

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
125694183 12569418 1 20160510 20160607 0