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
125676811 12567681 1 I 20160712 20160718 20160718 EXP US-BAUSCH-BL-2016-016842 BAUSCH AND LOMB 0.00 M Y 0.00000 20160718 PH 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
125676811 12567681 1 PS CARDIZEM CD DILTIAZEM HYDROCHLORIDE 1 Oral 20062 360 MG CAPSULES BID
125676811 12567681 2 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U 21392 TABLET
125676811 12567681 3 SS DILTIAZEM. DILTIAZEM 1 Oral U 20062

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125676811 12567681 1 Product used for unknown indication
125676811 12567681 2 Product used for unknown indication
125676811 12567681 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125676811 12567681 OT
125676811 12567681 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125676811 12567681 Atrioventricular block
125676811 12567681 Drug dose omission
125676811 12567681 Loss of consciousness

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
125676811 12567681 1 2014 0