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
127902021 12790202 1 I 201608 20160926 20160928 20160928 EXP US-ABBVIE-16K-163-1739573-00 ABBVIE 57.90 YR M Y 0.00000 20160928 CN COUNTRY NOT SPECIFIED US

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
127902021 12790202 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
127902021 12790202 2 SS LORTAB ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127902021 12790202 1 Crohn's disease
127902021 12790202 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127902021 12790202 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127902021 12790202 Coronary artery occlusion
127902021 12790202 Drug ineffective
127902021 12790202 Electrocardiogram abnormal
127902021 12790202 Vascular stent occlusion

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
127902021 12790202 1 2015 0