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
8622718 8746031 I 8622718-7 20030101 20120817 20120827 EXP US-JNJFOC-20120810150 JANSSEN BIOTECH, INC. 41 YR F Y 106.6 KG 20120827 CN UNITED STATES

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
8622718 1020666694 SS REMICADE 1 INTRAVENOUS UNKNOWN
8622718 1020666698 SS CORTISONE ACETATE 1 UNKNOWN
8622718 1020666696 SS ENBREL 1 UNKNOWN
8622718 1020666697 SS PREDNISONE TAB 1 UNKNOWN
8622718 1020666695 PS REMICADE 1 INTRAVENOUS EVERY 6 TO 8 WEEKS UNKNOWN
8622718 1020666699 C METHOTREXATE 1 ORAL
8622718 1020666700 C PREDNISONE TAB 1 ORAL
8622718 1020666701 C NORCO 1 ORAL 10-35 TABLETS ONE TO TWO TABLETS DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
8622718 1020666694 RHEUMATOID ARTHRITIS
8622718 1020666698 RHEUMATOID ARTHRITIS
8622718 1020666696 RHEUMATOID ARTHRITIS
8622718 1020666697 RHEUMATOID ARTHRITIS
8622718 1020666699 RHEUMATOID ARTHRITIS
8622718 1020666701 PAIN

Outcome of event

Event ID OUTC COD
8622718 OT

Reactions reported

Event ID PT
8622718 ALOPECIA
8622718 VITAMIN D DECREASED
8622718 CHILLS
8622718 SKIN ATROPHY
8622718 URTICARIA
8622718 HYPERSENSITIVITY
8622718 DIABETES MELLITUS
8622718 DRUG INEFFECTIVE
8622718 OSTEOARTHRITIS
8622718 CHEST DISCOMFORT
8622718 INSOMNIA
8622718 PRURITUS
8622718 ANIMAL SCRATCH
8622718 HEADACHE

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
8622718 1020666694 20120701
8622718 1020666695 20030101 20060101
8622718 1020666699 20030101
8622718 1020666700 20120501
8622718 1020666701 20070101