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
123299002 12329900 2 F 20160817 20160503 20160825 EXP CA-AMGEN-CANSP2016055569 AMGEN 0.00 F Y 0.00000 20160825 OT CA CA

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
123299002 12329900 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 UNKNOWN FORMULATION
123299002 12329900 2 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0 TABLET
123299002 12329900 3 SS ASPIRIN. ASPIRIN 1 Unknown UNK 0
123299002 12329900 4 SS DICLOFENAC DICLOFENAC 1 Unknown UNK 0
123299002 12329900 5 SS GOLD GOLD 1 Unknown UNK 0
123299002 12329900 6 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK 0
123299002 12329900 7 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
123299002 12329900 8 SS MOTRIN IBUPROFEN 1 Unknown UNK 0
123299002 12329900 9 SS NAPROSYN NAPROXEN 1 Unknown UNK 0
123299002 12329900 10 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
123299002 12329900 11 C TRAMADOL. TRAMADOL 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123299002 12329900 1 Rheumatoid arthritis
123299002 12329900 2 Rheumatoid arthritis
123299002 12329900 3 Rheumatoid arthritis
123299002 12329900 4 Rheumatoid arthritis
123299002 12329900 5 Rheumatoid arthritis
123299002 12329900 6 Rheumatoid arthritis
123299002 12329900 7 Rheumatoid arthritis
123299002 12329900 8 Rheumatoid arthritis
123299002 12329900 9 Rheumatoid arthritis
123299002 12329900 10 Rheumatoid arthritis
123299002 12329900 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123299002 12329900 OT
123299002 12329900 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123299002 12329900 Adverse reaction
123299002 12329900 Deafness transitory
123299002 12329900 Decreased appetite
123299002 12329900 Dizziness
123299002 12329900 Ear infection
123299002 12329900 Foot operation
123299002 12329900 Gastrointestinal pain
123299002 12329900 Headache
123299002 12329900 Hypophagia
123299002 12329900 Nausea
123299002 12329900 Pharyngitis
123299002 12329900 Shoulder arthroplasty
123299002 12329900 Vomiting
123299002 12329900 Weight decreased

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

no results found

Therapies reported

no results found