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
125704192 12570419 2 F 20160718 20160719 20160722 EXP CA-AMGEN-CANSP2016091154 AMGEN 0.00 F Y 0.00000 20160722 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
125704192 12570419 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 UNKNOWN FORMULATION
125704192 12570419 2 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0 TABLET
125704192 12570419 3 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK 0
125704192 12570419 4 SS FOLIC ACID. FOLIC ACID 1 Unknown UNK 0
125704192 12570419 5 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK 0 TABLET
125704192 12570419 6 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK 0
125704192 12570419 7 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125704192 12570419 8 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) UNK 0 UNKNOWN FORMULATION
125704192 12570419 9 SS PHTHALYLSULFATHIAZOLE PHTHALYLSULFATHIAZOLE 1 Unknown UNK 0
125704192 12570419 10 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
125704192 12570419 11 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
125704192 12570419 12 SS REACTIN DICLOFENAC SODIUM 1 Unknown UNK 0
125704192 12570419 13 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK 0
125704192 12570419 14 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK 0
125704192 12570419 15 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125704192 12570419 1 Product used for unknown indication
125704192 12570419 2 Product used for unknown indication
125704192 12570419 3 Product used for unknown indication
125704192 12570419 4 Product used for unknown indication
125704192 12570419 5 Product used for unknown indication
125704192 12570419 6 Product used for unknown indication
125704192 12570419 7 Product used for unknown indication
125704192 12570419 8 Product used for unknown indication
125704192 12570419 9 Product used for unknown indication
125704192 12570419 10 Product used for unknown indication
125704192 12570419 11 Product used for unknown indication
125704192 12570419 12 Product used for unknown indication
125704192 12570419 13 Product used for unknown indication
125704192 12570419 14 Rheumatoid arthritis
125704192 12570419 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125704192 12570419 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125704192 12570419 Abdominal discomfort
125704192 12570419 Alopecia
125704192 12570419 Exposure during pregnancy
125704192 12570419 Glossodynia
125704192 12570419 Hip arthroplasty
125704192 12570419 Knee arthroplasty
125704192 12570419 Pain
125704192 12570419 Pemphigus
125704192 12570419 Rheumatoid arthritis
125704192 12570419 Systemic lupus erythematosus

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

no results found

Therapies reported

no results found