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
122983182 12298318 2 F 2014 20160809 20160423 20160818 EXP US-ABBVIE-16K-163-1606927-00 ABBVIE 0.00 F Y 68.10000 KG 20160818 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
122983182 12298318 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
122983182 12298318 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
122983182 12298318 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
122983182 12298318 4 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
122983182 12298318 5 C METHOTREXATE. METHOTREXATE 1 0
122983182 12298318 6 C PREDNISONE. PREDNISONE 1 0 5 MG QD
122983182 12298318 7 C FOLIC ACID. FOLIC ACID 1 0
122983182 12298318 8 C VITAMIN C ASCORBIC ACID 1 0
122983182 12298318 9 C LISINOPRIL. LISINOPRIL 1 0
122983182 12298318 10 C MAGNESIUM MAGNESIUM 1 0
122983182 12298318 11 C VITAMIN D3 CHOLECALCIFEROL 1 0
122983182 12298318 12 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122983182 12298318 1 Rheumatoid arthritis
122983182 12298318 5 Rheumatoid arthritis
122983182 12298318 6 Rheumatoid arthritis
122983182 12298318 7 Product used for unknown indication
122983182 12298318 8 Product used for unknown indication
122983182 12298318 9 Hypertension
122983182 12298318 10 Product used for unknown indication
122983182 12298318 11 Product used for unknown indication
122983182 12298318 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122983182 12298318 OT
122983182 12298318 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122983182 12298318 Arthralgia
122983182 12298318 Chondropathy
122983182 12298318 Drug ineffective
122983182 12298318 Foot deformity
122983182 12298318 Gait disturbance
122983182 12298318 Herpes zoster
122983182 12298318 Intervertebral disc protrusion
122983182 12298318 Lumbar spinal stenosis
122983182 12298318 Neuroma
122983182 12298318 Osteoarthritis
122983182 12298318 Pneumonia
122983182 12298318 Pruritus
122983182 12298318 Thrombosis

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
122983182 12298318 1 20140306 0
122983182 12298318 2 201407 201408 0
122983182 12298318 3 201410 201506 0
122983182 12298318 4 20160324 0
122983182 12298318 6 2012 0