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
104657372 10465737 2 F 2013 20160801 20140920 20160815 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2014-BI-42478BP BOEHRINGER INGELHEIM 86.21 YR M Y 70.30000 KG 20160815 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
104657372 10465737 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 300 MG 404578 22512 150 MG CAPSULE BID
104657372 10465737 2 SS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 300 MG 404578 22512 150 MG CAPSULE BID
104657372 10465737 3 C PRAZOSIN PRAZOSIN 1 Oral 2 MG 0 2 MG TABLET QD
104657372 10465737 4 C PRAZOSIN PRAZOSIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104657372 10465737 1 Atrial flutter
104657372 10465737 2 Atrial fibrillation
104657372 10465737 3 Hypertension
104657372 10465737 4 Prostatic disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104657372 10465737 Blood urine present
104657372 10465737 Diarrhoea
104657372 10465737 Faeces discoloured
104657372 10465737 Gait disturbance
104657372 10465737 Off label use

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
104657372 10465737 1 2013 0
104657372 10465737 2 20131112 0