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
125671112 12567111 2 F 201604 20160727 20160718 20160805 PER US-PFIZER INC-2016320182 PFIZER 62.00 YR F Y 64.00000 KG 20160805 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
125671112 12567111 1 PS VERAPAMIL HCL VERAPAMIL HYDROCHLORIDE 1 240 MG, 1X/DAY Y 19152 240 MG MODIFIED-RELEASE TABLET QD
125671112 12567111 2 C DIGOXIN. DIGOXIN 1 0.125 MG, 1X/DAY (STARTED TAKING ABOUT 37 OR 38 YEARS AGO) 0 .125 MG QD
125671112 12567111 3 C ATENOLOL. ATENOLOL 1 0.25 MG, UNK (VENTRICULAR ISSUE STARTED TAKING 10 YEARS AGO) 0 .25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125671112 12567111 1 Supraventricular tachycardia
125671112 12567111 2 Supraventricular tachycardia
125671112 12567111 3 Ventricular dysfunction

Outcome of event

Event ID CASEID OUTC COD
125671112 12567111 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125671112 12567111 Heart rate decreased
125671112 12567111 Hypotension

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
125671112 12567111 1 201604 0