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
127403201 12740320 1 I 20110224 20160907 20160913 20160913 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00519 AMNEAL 63.00 YR F Y 76.19000 KG 20160913 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
127403201 12740320 1 PS NAPROXEN. NAPROXEN 1 UNK 75927
127403201 12740320 2 C JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 UNK 0
127403201 12740320 3 C AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 UNK 0
127403201 12740320 4 C VYTORIN EZETIMIBESIMVASTATIN 1 UNK 0
127403201 12740320 5 C Acetylsalicylic acid ASPIRIN 1 UNK 0
127403201 12740320 6 C LANTUS INSULIN GLARGINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127403201 12740320 1 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
127403201 12740320 HO
127403201 12740320 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127403201 12740320 Myocardial infarction

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
127403201 12740320 1 20101001 20110223 0
127403201 12740320 2 2010 0
127403201 12740320 3 2004 20110224 0
127403201 12740320 4 2006 0
127403201 12740320 5 2008 0
127403201 12740320 6 2010 0