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
127290481 12729048 1 I 2016 20160906 20160909 20160909 EXP US-SA-2016SA166616 AVENTIS 56.00 YR A M Y 0.00000 20160909 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
127290481 12729048 1 PS PRALUENT ALIROCUMAB 1 Unknown Y 6F035A 125559 75 MG QOW
127290481 12729048 2 SS NEURONTIN GABAPENTIN 1 Unknown U UNK 0
127290481 12729048 3 SS NEURONTIN GABAPENTIN 1 Unknown U UNK 0
127290481 12729048 4 C ALIROCUMAB PREFILLED PEN ALIROCUMAB 1 6F035A 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127290481 12729048 1 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
127290481 12729048 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127290481 12729048 Abdominal pain upper
127290481 12729048 Pancreatitis

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
127290481 12729048 1 201603 201608 0
127290481 12729048 2 2016 2016 0
127290481 12729048 3 2016 0
127290481 12729048 4 201603 201608 0