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
126140611 12614061 1 I 201601 20160201 20160802 20160802 EXP DE-ABBVIE-16K-062-1552888-00 ABBVIE 58.89 YR M Y 0.00000 20160802 CN COUNTRY NOT SPECIFIED DE

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
126140611 12614061 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
126140611 12614061 2 SS VOLTAREN DICLOFENAC SODIUM 1 Unknown U UNKNOWN 0 TABLET
126140611 12614061 3 C INSULINE INSULIN NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126140611 12614061 1 Ankylosing spondylitis
126140611 12614061 2 Pain in extremity
126140611 12614061 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126140611 12614061 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126140611 12614061 Bone loss
126140611 12614061 Fall
126140611 12614061 Feeling hot
126140611 12614061 Inflammation
126140611 12614061 Local swelling
126140611 12614061 Nausea
126140611 12614061 Pain in extremity
126140611 12614061 Syncope

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
126140611 12614061 1 20100201 0
126140611 12614061 2 201601 0