The Safety Rates Drug Report

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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
122501372 12250137 2 F 20160315 20160718 20160408 20160722 EXP DE-BFARM-16105000 DE-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-20741DE BOEHRINGER INGELHEIM 0.00 E M Y 70.00000 KG 20160722 MD COUNTRY NOT SPECIFIED DE

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
122501372 12250137 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 220 MG 22512 110 MG BID
122501372 12250137 2 C PREGABALIN. PREGABALIN 1 Oral 0 75 MG
122501372 12250137 3 C CIPRALEX ESCITALOPRAM OXALATE 1 Oral 0 10 MG
122501372 12250137 4 C RESTEX BENSERAZIDE 1 Oral RETARD 0
122501372 12250137 5 C VALDOXAN AGOMELATINE 1 Oral 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122501372 12250137 1 Atrial fibrillation
122501372 12250137 2 Pain
122501372 12250137 3 Depression
122501372 12250137 4 Product used for unknown indication
122501372 12250137 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
122501372 12250137 OT
122501372 12250137 DS
122501372 12250137 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122501372 12250137 Ischaemic stroke

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found