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
127006831 12700683 1 I 20160512 20160830 20160830 PER US-SA-2016SA095440 AVENTIS 78.00 YR E F Y 45.35000 KG 20160830 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
127006831 12700683 1 PS MULTAQ DRONEDARONE 1 Unknown Y Y UNK 22425 400 MG BID
127006831 12700683 2 SS MULTAQ DRONEDARONE 1 Unknown Y Y UNK 22425 400 MG BID
127006831 12700683 3 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 0 .5 DF TABLET BID
127006831 12700683 4 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 0 .5 DF TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127006831 12700683 1 Supraventricular tachycardia
127006831 12700683 2 Supraventricular tachycardia
127006831 12700683 3 Hypertension
127006831 12700683 4 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127006831 12700683 Blood pressure increased
127006831 12700683 Condition aggravated
127006831 12700683 Cystitis
127006831 12700683 Dizziness Dizziness
127006831 12700683 Drug dose omission
127006831 12700683 Hypoaesthesia Hypoaesthesia
127006831 12700683 Nausea Nausea
127006831 12700683 Pulse pressure increased
127006831 12700683 Stress

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
127006831 12700683 1 201511 201604 0
127006831 12700683 3 2014 0