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
127370171 12737017 1 I 20160413 20160906 20160913 20160913 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-58427BP BOEHRINGER INGELHEIM 87.65 YR M Y 0.00000 20160913 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
127370171 12737017 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 75 MG Y 22512 75 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127370171 12737017 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
127370171 12737017 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127370171 12737017 Asthenia
127370171 12737017 Chest pain
127370171 12737017 Dizziness
127370171 12737017 Dyspnoea
127370171 12737017 Full blood count decreased
127370171 12737017 Haematocrit decreased
127370171 12737017 Haemoglobin decreased
127370171 12737017 Loss of consciousness
127370171 12737017 Rectal 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
127370171 12737017 1 201601 201608 0