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
123353902 12335390 2 F 20140314 20160829 20160504 20160902 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-27381BI BOEHRINGER INGELHEIM 51.14 YR M Y 101.61000 KG 20160902 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
123353902 12335390 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 22512 150 MG CAPSULE BID
123353902 12335390 2 C LOPRESSOR METOPROLOL TARTRATE 1 Oral 50 MG 0 25 MG TABLET BID
123353902 12335390 3 C LOPRESSOR METOPROLOL TARTRATE 1 Oral 75 MG 0 25 MG TABLET TID
123353902 12335390 4 C LOPRESSOR METOPROLOL TARTRATE 1 Oral 100 MG 0 50 MG TABLET BID
123353902 12335390 5 C ASPIRIN. ASPIRIN 1 Oral ADULT LOW STRENGTH ; EC 0 81 MG TABLET QD
123353902 12335390 6 C MULTIVITAMIN VITAMINS 1 Oral 0 TABLET QD
123353902 12335390 7 C PRINIVIL LISINOPRIL 1 Oral 0 10 MG TABLET QD
123353902 12335390 8 C CARDIZEM CD DILTIAZEM HYDROCHLORIDE 1 Oral SR 0 120 MG CAPSULE QD
123353902 12335390 9 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 10 MG 0 10 MG TABLET QD
123353902 12335390 10 C ZESTRIL LISINOPRIL 1 Oral 0 10 MG TABLET QD
123353902 12335390 11 C CENTRUM SILVER MINERALSVITAMINS 1 Oral 0 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123353902 12335390 1 Atrial fibrillation
123353902 12335390 2 Hypertension
123353902 12335390 5 Product used for unknown indication
123353902 12335390 6 Product used for unknown indication
123353902 12335390 7 Hypertension
123353902 12335390 8 Hypertension
123353902 12335390 9 Product used for unknown indication
123353902 12335390 10 Hypertension
123353902 12335390 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123353902 12335390 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123353902 12335390 Cerebrovascular accident

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
123353902 12335390 1 20110613 0