The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5195450 6182812 F 5195450-2 20051101 20061201 20061230 EXP BE-ABBOTT-06P-013-0352187-00 ABBOTT F Y 20061230 MD BELGIUM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5195450 1007999495 PS HUMIRA 1 SUBCUTANEOUS UNKNOWN
5195450 1007999496 SS HUMIRA 1 UNKNOWN
5195450 1007999497 C METHOTREXATE 1
5195450 1007999498 C METHYLPREDNISOLONE 16MG TAB 1
5195450 1007999499 C FOLIC ACID 1
5195450 1007999500 C CELECOXIB 2
5195450 1007999502 C ZUMESTON 2
5195450 1007999503 C TRADONAL RETARD 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5195450 1007999495 RHEUMATOID ARTHRITIS
5195450 1007999497 RHEUMATOID ARTHRITIS
5195450 1007999498 RHEUMATOID ARTHRITIS
5195450 1007999499 RHEUMATOID ARTHRITIS
5195450 1007999500 RHEUMATOID ARTHRITIS
5195450 1007999502 DRUG USE FOR UNKNOWN INDICATION
5195450 1007999503 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
5195450 HO

Reactions reported

Event ID PT
5195450 OEDEMA PERIPHERAL
5195450 ROTATOR CUFF SYNDROME
5195450 TENDON RUPTURE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5195450 1007999495 20050802 20051101
5195450 1007999496 20060222