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
108937008 10893700 8 F 20150227 20160802 20150306 20160805 EXP ES-ABBVIE-15P-144-1354747-00 ABBVIE 37.00 YR F Y 58.00000 KG 20160805 OT COUNTRY NOT SPECIFIED ES

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
108937008 10893700 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
108937008 10893700 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 80 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
108937008 10893700 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
108937008 10893700 4 C CIPROFLOXACINO CIPROFLOXACIN HYDROCHLORIDE 1 Oral 0 500 MG BID
108937008 10893700 5 C ANSO 2 0 1 G BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108937008 10893700 1 Colitis ulcerative
108937008 10893700 4 Pain
108937008 10893700 5 Haemorrhoids

Outcome of event

Event ID CASEID OUTC COD
108937008 10893700 HO
108937008 10893700 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108937008 10893700 Abdominal pain
108937008 10893700 Abdominal pain upper
108937008 10893700 Anaemia

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
108937008 10893700 1 20141113 0
108937008 10893700 2 20150211 20150218 0
108937008 10893700 3 20150408 0
108937008 10893700 4 20150206 20150302 0
108937008 10893700 5 20160203 0