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
127006391 12700639 1 I 201509 20150929 20160830 20160830 PER US-SA-2015SA152470 AVENTIS 68.00 YR E F 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
127006391 12700639 1 PS MULTAQ DRONEDARONE 1 Unknown Y UNK 22425 400 MG TABLET BID
127006391 12700639 2 C PROCARDIA NIFEDIPINE 1 0 90 MG PILLULES QD
127006391 12700639 3 C DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 0 PILLULES QD
127006391 12700639 4 C GLIPIZIDE. GLIPIZIDE 1 0 5 MG PILLULES BID
127006391 12700639 5 C INVOKAMET CANAGLIFLOZINMETFORMIN HYDROCHLORIDE 1 0 PILLULES BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127006391 12700639 1 Atrial fibrillation
127006391 12700639 2 Blood pressure measurement
127006391 12700639 3 Blood pressure measurement
127006391 12700639 4 Diabetes mellitus
127006391 12700639 5 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127006391 12700639 Abdominal discomfort
127006391 12700639 Asthenia
127006391 12700639 Fatigue
127006391 12700639 Feeding disorder
127006391 12700639 Nausea
127006391 12700639 Vomiting

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
127006391 12700639 1 201509 201509 0