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
123726473 12372647 3 F 2016 20160803 20160516 20160824 PER US-PFIZER INC-2016223383 PFIZER 86.00 YR F Y 54.00000 KG 20160824 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
123726473 12372647 1 PS TIKOSYN DOFETILIDE 1 Oral 0.125 MG, 2X/DAY 4.0479999 MG 20931 .125 MG CAPSULE, HARD BID
123726473 12372647 2 SS TIKOSYN DOFETILIDE 1 Oral 125 UG, 2X/DAY 4.0479999 MG 20931 125 UG CAPSULE, HARD BID
123726473 12372647 3 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK 0
123726473 12372647 4 C METOPROLOL. METOPROLOL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123726473 12372647 1 Atrial fibrillation
123726473 12372647 3 Hypertension
123726473 12372647 4 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123726473 12372647 Agitation
123726473 12372647 Alopecia
123726473 12372647 Decreased appetite
123726473 12372647 Influenza like illness
123726473 12372647 Insomnia
123726473 12372647 Nasal congestion
123726473 12372647 Oropharyngeal pain
123726473 12372647 Restlessness

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
123726473 12372647 1 20160309 20160419 0
123726473 12372647 2 20160512 0
123726473 12372647 3 20150206 0
123726473 12372647 4 20150105 0