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
123617762 12361776 2 F 201604 20160613 20160512 20160809 PER US-SA-2016SA083235 AVENTIS 68.00 YR E F Y 0.00000 20160809 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
123617762 12361776 1 PS PRALUENT ALIROCUMAB 1 Unknown Y UNK 125559 75 MG INJECTION QOW
123617762 12361776 2 SS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Unknown Y UNK 0
123617762 12361776 3 C ALIROCUMAB PREFILLED PEN ALIROCUMAB 1 Unknown UNK 0 QOW
123617762 12361776 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123617762 12361776 1 Blood cholesterol increased
123617762 12361776 2 Bronchitis
123617762 12361776 3 Blood cholesterol increased
123617762 12361776 4 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123617762 12361776 Bronchitis
123617762 12361776 Malaise
123617762 12361776 Rash
123617762 12361776 Urticaria

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
123617762 12361776 1 20160304 20160415 0
123617762 12361776 2 20160416 20160418 0
123617762 12361776 3 20160304 20160415 0