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
125942681 12594268 1 I 20160505 20160719 20160726 20160726 EXP FR-TAKEDA-2016TEU003906 TAKEDA 80.00 YR F Y 0.00000 20160726 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
125942681 12594268 1 SS EUPANTOL PANTOPRAZOLE SODIUM 1 Oral 40 MG, QD 0 40 MG ENTERIC COATED TABLET QD
125942681 12594268 2 PS COLCHICINE. COLCHICINE 1 Oral 0.5 MG, QD 16 MG Y 22352 .5 MG QD
125942681 12594268 3 SS ALLOPURINOL. ALLOPURINOL 1 Oral UNK, QD 0 QD
125942681 12594268 4 SS COUMADINE WARFARIN SODIUM 1 Oral 2 MG, QD 78 MG Y 0 2 MG TABLET QD
125942681 12594268 5 SS CORDARONE AMIODARONE HYDROCHLORIDE 1 Oral UNK UNK, QD 0 QD
125942681 12594268 6 C TEMERIT NEBIVOLOL 1 Oral 5 MG, UNK U 0 5 MG
125942681 12594268 7 C TEMESTA /00273201/ LORAZEPAM 1 Oral 1 MG, BID U 0 1 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125942681 12594268 1 Product used for unknown indication
125942681 12594268 2 Gout
125942681 12594268 3 Gout
125942681 12594268 4 Atrial fibrillation
125942681 12594268 5 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125942681 12594268 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125942681 12594268 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
125942681 12594268 2 20160404 20160509 0
125942681 12594268 3 20160425 0
125942681 12594268 4 20160328 20160507 0