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
102766162 10276616 2 F 2013 20160726 20140703 20160803 EXP BR-ABBVIE-14P-020-1253503-00 ABBVIE 0.00 F Y 73.00000 KG 20160803 CN COUNTRY NOT SPECIFIED BR

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
102766162 10276616 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y 32416LX03 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
102766162 10276616 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y 32416LX03 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
102766162 10276616 3 SS CHLOROQUINE. CHLOROQUINE 1 Unknown U UNKNOWN 0
102766162 10276616 4 C PIROXICAM/DIPIRONE/FAMOTIDINE/CODEINE/NORTRIPTYLINE 2 Oral 0 TABLET
102766162 10276616 5 C PREDNISONE. PREDNISONE 1 Oral 0 TABLET
102766162 10276616 6 C CLONAZEPAM. CLONAZEPAM 1 Oral 0 TABLET
102766162 10276616 7 C MIRACALCIO VIT D 2 Oral EVERY NIGHT 0 TABLET QD
102766162 10276616 8 C ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 0 TABLET /wk
102766162 10276616 9 C METHOTREXATE. METHOTREXATE 1 Oral EVERY WEDNESDAY 0 1 DF TABLET
102766162 10276616 10 C METHOTREXATE. METHOTREXATE 1 0
102766162 10276616 11 C FOLIC ACID. FOLIC ACID 1 Oral EVERY THURSDAY 0 1 DF TABLET /wk
102766162 10276616 12 C FOLIC ACID. FOLIC ACID 1 0
102766162 10276616 13 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 TABLET
102766162 10276616 14 C CEFALINA 2 Oral 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102766162 10276616 1 Rheumatoid arthritis
102766162 10276616 3 Product used for unknown indication
102766162 10276616 4 Pain
102766162 10276616 5 Arthritis
102766162 10276616 6 Sleep disorder therapy
102766162 10276616 7 Osteoporosis
102766162 10276616 8 Osteoporosis
102766162 10276616 9 Arthritis
102766162 10276616 10 Rheumatoid arthritis
102766162 10276616 11 Arthritis
102766162 10276616 12 Complement factor
102766162 10276616 13 Gastric disorder
102766162 10276616 14 Antidepressant therapy

Outcome of event

Event ID CASEID OUTC COD
102766162 10276616 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102766162 10276616 Arthropathy
102766162 10276616 Exostosis
102766162 10276616 Eyelid disorder
102766162 10276616 Intervertebral disc protrusion
102766162 10276616 Ligament rupture
102766162 10276616 Meniscus injury
102766162 10276616 Osteoarthritis
102766162 10276616 Pain
102766162 10276616 Spinal disorder

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
102766162 10276616 1 20110101 0
102766162 10276616 7 1996 0
102766162 10276616 8 1996 0
102766162 10276616 9 2011 0
102766162 10276616 11 2011 0
102766162 10276616 14 2012 0