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
125190681 12519068 1 I 20160623 20160701 20160701 EXP US-ABBVIE-16K-163-1661208-00 ABBVIE 0.00 M Y 0.00000 20160630 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
125190681 12519068 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous 1053686 125057 SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
125190681 12519068 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous 1053686 125057 SOLUTION FOR INJECTION IN PRE-FILLED PEN
125190681 12519068 3 SS IMURAN AZATHIOPRINE 1 Unknown U UNKNOWN 0
125190681 12519068 4 C LISINOPRIL. LISINOPRIL 1 0
125190681 12519068 5 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125190681 12519068 1 Crohn's disease
125190681 12519068 3 Product used for unknown indication
125190681 12519068 4 Product used for unknown indication
125190681 12519068 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125190681 12519068 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125190681 12519068 Drug ineffective
125190681 12519068 Gastrointestinal obstruction

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found