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
126734981 12673498 1 I 20160701 20160810 20160822 20160822 EXP FR-PFIZER INC-2016391263 PFIZER 66.00 YR F Y 0.00000 20160822 OT FR FR

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
126734981 12673498 1 PS AMIODARONE HCL AMIODARONE HYDROCHLORIDE 1 Oral 200MG PER DAY 5 D/ 7 18972 200 MG
126734981 12673498 2 I AMIODARONE HCL AMIODARONE HYDROCHLORIDE 1 Oral 400 MG IN THE MORNING 5 DAY/7 18972 400 MG
126734981 12673498 3 SS PREVISCAN FLUINDIONE 1 Oral UNK 0
126734981 12673498 4 C WARFARIN WARFARIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126734981 12673498 1 Atrial fibrillation
126734981 12673498 3 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126734981 12673498 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126734981 12673498 Cardiac failure
126734981 12673498 Drug interaction
126734981 12673498 Haematoma
126734981 12673498 International normalised ratio 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
126734981 12673498 2 20160427 0
126734981 12673498 3 201505 0