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
124648134 12464813 4 F 20160804 20160614 20160816 EXP US-PFIZER INC-2016289110 PFIZER 75.00 YR F Y 102.00000 KG 20160816 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
124648134 12464813 1 PS TIKOSYN DOFETILIDE 1 125 MG, 2X/DAY, (ONE IN MORNING AND ONE IN EVENING) 20931 125 MG CAPSULE, HARD BID
124648134 12464813 2 SS TIKOSYN DOFETILIDE 1 250 MG, DAILY 20931 250 MG CAPSULE, HARD
124648134 12464813 3 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 100 MG, 2X/DAY N 74133 100 MG BID
124648134 12464813 4 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 25 MG, 2X/DAY N 74133 25 MG BID

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
124648134 12464813 OT
124648134 12464813 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124648134 12464813 Angina pectoris
124648134 12464813 Asthenia
124648134 12464813 Atrial fibrillation
124648134 12464813 Dizziness
124648134 12464813 Drug ineffective
124648134 12464813 Visual impairment
124648134 12464813 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
124648134 12464813 1 201605 0