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
118465222 11846522 2 F 2015 20160202 20151217 20160210 EXP CA-ABBVIE-15K-028-1460868-00 ABBVIE 45.54 YR F Y 81.72000 KG 20160210 MD 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
118465222 11846522 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous 6052375,6053765 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
118465222 11846522 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous 6052375,6053765 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
118465222 11846522 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0 40 MG BID
118465222 11846522 4 C SEROQUEL QUETIAPINE FUMARATE 1 0
118465222 11846522 5 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118465222 11846522 1 Crohn's disease
118465222 11846522 3 Gastrooesophageal reflux disease
118465222 11846522 4 Product used for unknown indication
118465222 11846522 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118465222 11846522 HO
118465222 11846522 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118465222 11846522 Drug effect incomplete
118465222 11846522 Drug ineffective
118465222 11846522 Ileal stenosis

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
118465222 11846522 1 20150715 0
118465222 11846522 2 2015 20151118 0