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
127006421 12700642 1 I 201509 20151005 20160830 20160830 PER US-SA-2015SA160073 AVENTIS 61.00 YR A M Y 0.00000 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
127006421 12700642 1 PS MULTAQ DRONEDARONE 1 Oral Y UNKNOWN 22425 400 MG TABLET BID
127006421 12700642 2 C IBUPROFEN. IBUPROFEN 1 0 200 MG
127006421 12700642 3 C ATENOLOL. ATENOLOL 1 0 25 MG
127006421 12700642 4 C LIPITOR ATORVASTATIN CALCIUM 1 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127006421 12700642 1 Atrial fibrillation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127006421 12700642 Chest discomfort
127006421 12700642 Condition aggravated
127006421 12700642 Cough
127006421 12700642 Feeling abnormal
127006421 12700642 Palpitations

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
127006421 12700642 1 20150919 20151002 0