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
125768801 12576880 1 I 20160712 20160720 20160720 EXP CA-PFIZER INC-2016350830 PFIZER 0.00 F Y 0.00000 20160720 CN 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
125768801 12576880 1 SS ENBREL ETANERCEPT 1 Subcutaneous UNK U 0
125768801 12576880 2 PS METHOTREXATE. METHOTREXATE 1 Unknown UNK U 11719
125768801 12576880 3 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK U 7073
125768801 12576880 4 SS FOLIC ACID. FOLIC ACID 1 Unknown UNK U 0
125768801 12576880 5 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK U 0
125768801 12576880 6 SS ARAVA LEFLUNOMIDE 1 Unknown UNK U 0 TABLET
125768801 12576880 7 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous UNK U 0
125768801 12576880 8 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK U 0 TABLET
125768801 12576880 9 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
125768801 12576880 10 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) UNK U 0
125768801 12576880 11 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK U 0 TABLET
125768801 12576880 12 SS PREDNISONE. PREDNISONE 1 Unknown UNK U 0
125768801 12576880 13 SS REACTINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNK U 0
125768801 12576880 14 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK U 0
125768801 12576880 15 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK U 0
125768801 12576880 16 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125768801 12576880 1 Rheumatoid arthritis
125768801 12576880 2 Rheumatoid arthritis
125768801 12576880 3 Rheumatoid arthritis
125768801 12576880 5 Rheumatoid arthritis
125768801 12576880 6 Rheumatoid arthritis
125768801 12576880 7 Rheumatoid arthritis
125768801 12576880 8 Rheumatoid arthritis
125768801 12576880 9 Rheumatoid arthritis
125768801 12576880 10 Rheumatoid arthritis
125768801 12576880 11 Rheumatoid arthritis
125768801 12576880 12 Rheumatoid arthritis
125768801 12576880 14 Rheumatoid arthritis
125768801 12576880 15 Rheumatoid arthritis
125768801 12576880 16 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125768801 12576880 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125768801 12576880 Abdominal discomfort
125768801 12576880 Alopecia
125768801 12576880 Fatigue
125768801 12576880 Glossodynia
125768801 12576880 Hand deformity
125768801 12576880 Pain
125768801 12576880 Pemphigus
125768801 12576880 Swelling
125768801 12576880 Systemic lupus erythematosus
125768801 12576880 Wound

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

no results found

Therapies reported

no results found