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
121431716 12143171 6 F 201510 20160913 20160304 20160922 EXP US-ABBVIE-16K-163-1568667-00 ABBVIE 52.13 YR F Y 0.00000 20160922 MD 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
121431716 12143171 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
121431716 12143171 2 SS METHOTREXATE. METHOTREXATE 1 Unknown DIVIDED DOSE (UNKNOWN MG) ON SAT AND SUN U UNKNOWN 0
121431716 12143171 3 C PREDNISONE. PREDNISONE 1 Oral 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121431716 12143171 1 Rheumatoid arthritis
121431716 12143171 2 Rheumatoid arthritis
121431716 12143171 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
121431716 12143171 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121431716 12143171 Abdominal pain
121431716 12143171 Alopecia
121431716 12143171 Anaemia
121431716 12143171 Blood pressure decreased
121431716 12143171 Cataract
121431716 12143171 Contusion
121431716 12143171 Disseminated intravascular coagulation
121431716 12143171 Drug ineffective
121431716 12143171 Fall
121431716 12143171 Hypersomnia
121431716 12143171 Intra-abdominal haematoma
121431716 12143171 Loss of consciousness
121431716 12143171 Nausea
121431716 12143171 Pyrexia
121431716 12143171 Rash macular
121431716 12143171 Renal failure
121431716 12143171 Rheumatoid arthritis
121431716 12143171 Sepsis
121431716 12143171 Tibia fracture

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
121431716 12143171 1 201510 20160213 0