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
123205423 12320542 3 F 20160922 20160429 20160926 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-27351BI BOEHRINGER INGELHEIM 0.00 M Y 0.00000 20160926 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
123205423 12320542 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Unknown 150 MG 22512 75 MG CAPSULE BID
123205423 12320542 2 C DILTIAZEM. DILTIAZEM 1 Oral 180 MG 0 180 MG QD
123205423 12320542 3 C ISOSORBIDE. ISOSORBIDE 1 Oral 30 MG 0 30 MG QD
123205423 12320542 4 C LASIX FUROSEMIDE 1 Oral 40 MG 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123205423 12320542 1 Atrial fibrillation
123205423 12320542 2 Product used for unknown indication
123205423 12320542 3 Product used for unknown indication
123205423 12320542 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123205423 12320542 DE
123205423 12320542 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123205423 12320542 Anaemia
123205423 12320542 Gastrointestinal haemorrhage
123205423 12320542 Haemorrhoidal haemorrhage

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
123205423 12320542 1 201201 20130416 0