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
125721681 12572168 1 I 20160712 20160719 20160719 EXP CA-PFIZER INC-2016348201 PFIZER 0.00 F Y 0.00000 20160719 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
125721681 12572168 1 SS ENBREL ETANERCEPT 1 UNK U 0
125721681 12572168 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK U 11719
125721681 12572168 3 SS REMICADE INFLIXIMAB 1 UNK U 0
125721681 12572168 4 SS ACTEMRA TOCILIZUMAB 1 UNK U 0
125721681 12572168 5 SS ARAVA LEFLUNOMIDE 1 UNK U 0 TABLET
125721681 12572168 6 SS CORTISONE ACETATE. CORTISONE ACETATE 1 25 MG, UNK U 0 25 MG TABLET
125721681 12572168 7 SS FOLIC ACID. FOLIC ACID 1 1 MG, UNK U 0 1 MG TABLET
125721681 12572168 8 SS FOSAMAX ALENDRONATE SODIUM 1 UNK U 0 TABLET
125721681 12572168 9 SS HUMIRA ADALIMUMAB 1 UNK U 0
125721681 12572168 10 SS ORENCIA ABATACEPT 1 UNK U 0
125721681 12572168 11 SS PHTHALYLSULFATHIAZOLE PHTHALYLSULFATHIAZOLE 1 UNK U 0
125721681 12572168 12 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK U 0 TABLET
125721681 12572168 13 SS PREDNISONE. PREDNISONE 1 UNK U 0
125721681 12572168 14 SS REACTINE CETIRIZINE HYDROCHLORIDE 1 Unknown UNK U 0
125721681 12572168 15 SS RITUXAN RITUXIMAB 1 UNK U 0
125721681 12572168 16 SS SIMPONI GOLIMUMAB 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125721681 12572168 1 Rheumatoid arthritis
125721681 12572168 2 Rheumatoid arthritis
125721681 12572168 3 Rheumatoid arthritis
125721681 12572168 4 Rheumatoid arthritis
125721681 12572168 5 Rheumatoid arthritis
125721681 12572168 6 Rheumatoid arthritis
125721681 12572168 7 Rheumatoid arthritis
125721681 12572168 9 Rheumatoid arthritis
125721681 12572168 10 Rheumatoid arthritis
125721681 12572168 11 Rheumatoid arthritis
125721681 12572168 12 Rheumatoid arthritis
125721681 12572168 15 Rheumatoid arthritis
125721681 12572168 16 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125721681 12572168 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125721681 12572168 Abdominal discomfort
125721681 12572168 Alopecia
125721681 12572168 Fatigue
125721681 12572168 Glossodynia
125721681 12572168 Pain
125721681 12572168 Pemphigus
125721681 12572168 Swelling
125721681 12572168 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