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
102563726 10256372 6 F 201306 20160826 20140624 20160830 EXP TR-ABBVIE-14P-161-1250484-00 ABBVIE 42.95 YR M Y 100.00000 KG 20160830 OT COUNTRY NOT SPECIFIED TR

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
102563726 10256372 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous N UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
102563726 10256372 2 C RAMIPRIL + HYDROCHLOROTHIAZIDE (DELIX) 2 0 10 MG QD
102563726 10256372 3 C LUSTRAL SERTRALINE HYDROCHLORIDE 1 Oral 0 100 MG QD
102563726 10256372 4 C MUSCORIL THIOCOLCHICOSIDE 1 Oral 0 8 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102563726 10256372 1 Ankylosing spondylitis
102563726 10256372 2 Hypertension
102563726 10256372 3 Ankylosing spondylitis
102563726 10256372 4 Ankylosing spondylitis

Outcome of event

Event ID CASEID OUTC COD
102563726 10256372 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
102563726 10256372 Nephritis
102563726 10256372 Pain
102563726 10256372 Renal failure

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
102563726 10256372 1 20130114 201504 0