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
127766221 12776622 1 I 2016 20160919 20160923 20160923 EXP US-ABBVIE-16K-163-1735016-00 ABBVIE 0.00 M Y 55.39000 KG 20160923 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
127766221 12776622 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
127766221 12776622 2 SS PREDNISONE. PREDNISONE 1 Unknown D U UNKNOWN 0
127766221 12776622 3 SS PREDNISONE. PREDNISONE 1 Unknown D U UNKNOWN 0
127766221 12776622 4 C METHOTREXATE. METHOTREXATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127766221 12776622 1 Rheumatoid arthritis
127766221 12776622 2 Product used for unknown indication
127766221 12776622 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127766221 12776622 DS
127766221 12776622 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127766221 12776622 Decreased appetite
127766221 12776622 Increased tendency to bruise
127766221 12776622 Pneumothorax
127766221 12776622 Pulmonary oedema
127766221 12776622 Weight decreased

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
127766221 12776622 1 2016 20160905 0
127766221 12776622 4 20160918 0