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
125700071 12570007 1 I 20160119 0 20160718 20160718 DIR 53.00 YR M N 247.00000 LBS 20160716 N 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
125700071 12570007 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 1 INJECTION 2WEEKS INJECTED UNDER THE SKIN N D 20170101 0 1 DF SUSPENSION FOR INJECTION
125700071 12570007 3 C METAFORMIN 2 0
125700071 12570007 5 C LIPITOR ATORVASTATIN CALCIUM 1 0
125700071 12570007 7 C DIAVAN HCT 2 0
125700071 12570007 9 C VITAMIN D CHOLECALCIFEROL 1 0
125700071 12570007 11 C IBOPHROFEN 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125700071 12570007 1 Ankylosing spondylitis

Outcome of event

Event ID CASEID OUTC COD
125700071 12570007 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125700071 12570007 Bronchitis
125700071 12570007 Impaired work ability
125700071 12570007 Psoriasis
125700071 12570007 Rash

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
125700071 12570007 1 20151115 20160115 2 WK