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
122776494 12277649 4 F 20160331 20160715 20160418 20160719 EXP CO-ABBVIE-16K-036-1606853-00 ABBVIE 23.27 YR F Y 45.00000 KG 20160719 CN COUNTRY NOT SPECIFIED CO

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
122776494 12277649 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
122776494 12277649 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y U UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED PEN
122776494 12277649 3 C MORPHINE MORPHINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122776494 12277649 1 Ankylosing spondylitis
122776494 12277649 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122776494 12277649 HO
122776494 12277649 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122776494 12277649 Chronic gastritis
122776494 12277649 Neurogenic bladder
122776494 12277649 Pancreatitis
122776494 12277649 Pneumonia

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
122776494 12277649 1 20160303 20160418 0
122776494 12277649 2 20160712 0