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
122659112 12265911 2 F 2016 20160719 20160413 20160727 EXP CA-ABBVIE-16K-028-1602343-00 ABBVIE 63.87 YR F Y 0.00000 20160727 CN COUNTRY NOT SPECIFIED CA

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
122659112 12265911 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous N U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
122659112 12265911 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous N U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
122659112 12265911 3 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown N UNKNOWN 0
122659112 12265911 4 SS LOVENOX ENOXAPARIN SODIUM 1 N UNKNOWN 0
122659112 12265911 5 SS LOVENOX ENOXAPARIN SODIUM 1 N UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122659112 12265911 1 Rheumatoid arthritis
122659112 12265911 3 Post procedural haemorrhage
122659112 12265911 4 Postoperative care
122659112 12265911 5 Femur fracture

Outcome of event

Event ID CASEID OUTC COD
122659112 12265911 OT
122659112 12265911 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122659112 12265911 Femur fracture
122659112 12265911 Haemorrhage
122659112 12265911 Headache
122659112 12265911 Nasopharyngitis
122659112 12265911 Rheumatoid arthritis

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
122659112 12265911 1 20120119 2016 0
122659112 12265911 2 2016 0
122659112 12265911 3 2016 2016 0