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
123867873 12386787 3 F 2016 20160728 20160519 20160801 EXP CA-ABBVIE-16K-028-1631038-00 ABBVIE 58.03 YR M Y 56.75000 KG 20160801 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
123867873 12386787 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
123867873 12386787 2 C IMURAN AZATHIOPRINE 1 Oral 0 50 MG TID
123867873 12386787 3 C PENTASA MESALAMINE 1 Oral 0 1 G BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123867873 12386787 1 Crohn's disease
123867873 12386787 2 Crohn's disease
123867873 12386787 3 Crohn's disease

Outcome of event

Event ID CASEID OUTC COD
123867873 12386787 DE
123867873 12386787 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123867873 12386787 Acute respiratory distress syndrome
123867873 12386787 Bronchopulmonary aspergillosis
123867873 12386787 Crohn's disease
123867873 12386787 Intestinal obstruction
123867873 12386787 Pulmonary embolism
123867873 12386787 Respiratory moniliasis
123867873 12386787 Septic shock
123867873 12386787 Staphylococcal bacteraemia

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
123867873 12386787 1 20160401 0
123867873 12386787 2 20160309 0
123867873 12386787 3 201407 0